Product Name

  • Name

    3-Nitrochlorobenzene

  • EINECS 204-496-1
  • CAS No. 121-73-3
  • Article Data134
  • CAS DataBase
  • Density 1.534 g/cm3
  • Solubility insoluble in water
  • Melting Point 43-47 °C(lit.)
  • Formula C6H4ClNO2
  • Boiling Point 236 °C at 760 mmHg
  • Molecular Weight 157.556
  • Flash Point 103.3 °C
  • Transport Information UN 1578 6.1/PG 2
  • Appearance Moist tan or pale yellow crystalline solid
  • Safety 22-24/25-60-61-45-38-36/37/39-28A
  • Risk Codes 22-50/53-23/24/25
  • Molecular Structure Molecular Structure of 121-73-3 (3-Nitrochlorobenzene)
  • Hazard Symbols ToxicT,HarmfulXn,DangerousN
  • Synonyms 1-Chloro-3-nitrobenzene;3-Chloro-1-nitrobenzene;3-Chloronitrobenzene;3-Nitro-1-chlorobenzene;3-Nitrophenyl chloride;NSC 5502;m-Chloronitrobenzene;m-Nitrochlorobenzene;
  • PSA 45.82000
  • LogP 2.77140

Synthetic route

m-nitrobenzene boronic acid
13331-27-6

m-nitrobenzene boronic acid

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With 1,3-dichloro-5,5-dimethylhydantoin; copper(l) chloride In acetonitrile at 80℃; for 2h;98%
With N-chloro-succinimide In acetonitrile at 80℃; for 12h;97%
With 1,3-dichloro-5,5-dimethylhydantoin; sodium methylate In methanol; water; acetonitrile at 60℃;43 % Chromat.
4-Chloro-2-nitroaniline
89-63-4

4-Chloro-2-nitroaniline

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With tetrahydrofuran; tert.-butylnitrite; dimethyl sulfoxide at 30℃; for 1h; Green chemistry;96%
3-Bromonitrobenzene
585-79-5

3-Bromonitrobenzene

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With copper(I) oxide; tetramethlyammonium chloride; L-proline In ethanol at 110℃; for 20h; Inert atmosphere;93%
With lithium chloride In water; acetic acid Irradiation;90%
With hydrogenchloride; lithium chloride In water; acetonitrile at 20℃; Product distribution; Mechanism; Irradiation; investigation of nucleophilic aromatic photosubstitution at different H+ and Cl- ion concentration;90%
3-chloro-aniline
108-42-9

3-chloro-aniline

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With 1,9-diperoxynonanedioic acid In acetonitrile at 50℃; for 0.5h;92%
With 3-chloro-benzenecarboperoxoic acid In 1,2-dichloro-ethane for 10h; Reflux;81%
With tert.-butylhydroperoxide; potassium iodide In water; acetonitrile at 80℃; for 15h;70%
2-Chloro-4-nitroaniline
121-87-9

2-Chloro-4-nitroaniline

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With tetrahydrofuran; tert.-butylnitrite; dimethyl sulfoxide at 30℃; for 1h; Green chemistry;92%
Stage #1: 2-Chloro-4-nitroaniline With Nitrogen dioxide In acetonitrile at -20℃; Diazotization;
Stage #2: With calcium bis(hypophosphite); Fe2SO4*7H2O In methanol; acetonitrile at 20℃; Dediazonation;
87%
With sulfuric acid; ethyl acetate; sodium nitrite In water at 50 - 55℃; for 0.5h;50%
Multi-step reaction with 3 steps
1: 98 percent / i-pentyl nitrite; HOAc / 0 - 5 °C
2: 91 percent / aq. NaOH / 0.5 h / 0 - 5 °C
3: 9 percent / aq. HBr / acetonitrile / 0.5 h / 60 °C
View Scheme
Multi-step reaction with 3 steps
1: 98 percent / i-pentyl nitrite; HOAc / 0 - 5 °C
2: 91 percent / aq. NaOH / 0.5 h / 0 - 5 °C
3: 2 percent / aq. HI; HBF4 / acetonitrile / 0.5 h / 60 °C
View Scheme
nitrobenzene
98-95-3

nitrobenzene

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With N-chloro-succinimide; iron(III) chloride for 3h;91%
With trichloroisocyanuric acid; sulfuric acid at 80℃; for 5h;80%
With N-chloro-succinimide; boron trifluoride at 100 - 105℃; for 24h;69%
3-chlorophenylboronic acid
63503-60-6

3-chlorophenylboronic acid

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With Iron(III) nitrate nonahydrate In toluene at 80℃; for 18h; Inert atmosphere;88%
With zirconium(IV) oxynitrate hydrate; iodine In toluene at 20℃; for 18h; Inert atmosphere;87%
With copper(I) oxide; ammonium hydroxide; oxygen; sodium nitrite In water at 25℃; for 36h;60%
With chloro-trimethyl-silane; silver nitrate In dichloromethane at 20℃; for 72h;90 % Spectr.
potassium 3-nitrophenyltrifluoroborate

potassium 3-nitrophenyltrifluoroborate

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With trichloroisocyanuric acid In water; ethyl acetate at 80℃; for 4h; Open flask;85%
mesityl(3-nitrophenyl)iodonium trifluoromethanesulfonate
1415642-81-7

mesityl(3-nitrophenyl)iodonium trifluoromethanesulfonate

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With copper(l) chloride In acetonitrile at 80℃; for 2h;85%
3-chlorobenzoate
535-80-8

3-chlorobenzoate

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With nitronium tetrafluoborate; silver carbonate In N,N-dimethyl acetamide at 90℃; for 12h; Inert atmosphere; Schlenk technique; regioselective reaction;80%
4-chloro-2-nitro-benzoic acid
6280-88-2

4-chloro-2-nitro-benzoic acid

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With copper(l) iodide; triethylamine In dimethyl sulfoxide at 120℃; under 760.051 Torr; for 20h; Inert atmosphere; Schlenk technique;79%
With 2.9-dimethyl-1,10-phenanthroline; oxygen; copper (I) acetate; silver sulfate; sodium bromide In dimethyl sulfoxide at 160℃; for 24h; Schlenk technique;64%
With copper(I) oxide; N,N,N,N,-tetramethylethylenediamine In 1-methyl-pyrrolidin-2-one at 140℃; for 0.333333h; Inert atmosphere;83 %Chromat.
With copper(I) oxide at 120℃; for 24h; Ionic liquid;
Multi-step reaction with 3 steps
1: acetonitrile / 2 h / 20 °C / Darkness
2: acetonitrile / Darkness
3: water / d7-N,N-dimethylformamide / 0.67 h / 100 °C / Inert atmosphere; Glovebox; Sealed tube; Darkness
View Scheme
nitrobenzene
98-95-3

nitrobenzene

A

m-iodonitrobenzene
645-00-1

m-iodonitrobenzene

B

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With sulfuric acid; water; Iodine monochloride; silver sulfate at 20℃; for 0.25h; Yields of byproduct given;A 74%
B n/a
With sulfuric acid; water; Iodine monochloride; silver sulfate at 20℃; for 0.25h; Yield given;A 74%
B n/a
With sulfuric acid; Iodine monochloride; fluorine Ambient temperature;A 45%
B 44%
C10H13ClN4O2
401631-87-6

C10H13ClN4O2

A

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

B

1-bromo-2-chloro-4-nitrobenzene
29682-39-1

1-bromo-2-chloro-4-nitrobenzene

Conditions
ConditionsYield
With hydrogen bromide In acetonitrile at 60℃; for 0.5h;A 9%
B 74%
C10H13ClN4O2
401631-87-6

C10H13ClN4O2

A

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

B

3-chloro-4-iodonitrobenzene
41252-96-4

3-chloro-4-iodonitrobenzene

Conditions
ConditionsYield
With tetrafluoroboric acid; hydrogen iodide In acetonitrile at 60℃; for 0.5h;A 2%
B 74%
3-nitrobenzenediazonium o-benzenedisulfonimide

3-nitrobenzenediazonium o-benzenedisulfonimide

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With N-benzyl-N,N,N-triethylammonium chloride; copper In acetonitrile at 20℃; for 0.75h; Substitution;72%
With N-benzyl-N,N,N-triethylammonium chloride In acetonitrile at 60℃; for 0.75h; Substitution;19%
3-nitro-aniline
99-09-2

3-nitro-aniline

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With tert.-butylnitrite; N-benzyl-N,N,N-triethylammonium chloride; toluene-4-sulfonic acid; copper dichloride In acetonitrile at 60℃; for 1h;66%
With tert.-butylnitrite; N-benzyl-N,N,N-triethylammonium chloride; toluene-4-sulfonic acid; copper dichloride65%
With tert.-butylnitrite; N-benzyl-N,N,N-triethylammonium chloride; copper dichloride; 10-camphorsulfonic acid In neat (no solvent) Time; Solvent;65%
methyl 4-chloro-2-nitrobenzoate
42087-80-9

methyl 4-chloro-2-nitrobenzoate

A

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

B

4-chloro-2-fluorobenzoic acid methyl ester

4-chloro-2-fluorobenzoic acid methyl ester

Conditions
ConditionsYield
With potassium fluoride; tetraphenylphosphonium bromide In sulfolane at 220℃; for 0.5h; Product distribution; other chloronitroaromatic compounds, other reagents and solvents, var. temp. and time;A 66%
B 27%
With potassium fluoride; tetraphenylphosphonium bromide In sulfolane at 220℃; for 0.5h;A 66 % Chromat.
B 27 % Chromat.
(R,S)-1-(4-chloro-2-nitrophenyl)ethanol
787633-79-8

(R,S)-1-(4-chloro-2-nitrophenyl)ethanol

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With 1,10-Phenanthroline; oxygen; copper diacetate; silver nitrate; sodium hydroxide In dimethyl sulfoxide at 140℃; under 3750.38 Torr; for 12h; Autoclave; Green chemistry;48%
3-chloro-N,N-dimethylaniline
6848-13-1

3-chloro-N,N-dimethylaniline

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With tert.-butylhydroperoxide; ammonium iodide; water In dimethyl sulfoxide at 90℃; for 4h; Sealed tube;38%
meta-nitrophenol
554-84-7

meta-nitrophenol

dichlorotriphenoxyphosphorane
15493-07-9

dichlorotriphenoxyphosphorane

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
at 120 - 140℃; anschliessendes Erhitzen auf 250-350grad;
acetic anhydride
108-24-7

acetic anhydride

3-nitro-benzenediazonium; pentachloro plumbate(III)

3-nitro-benzenediazonium; pentachloro plumbate(III)

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

3-nitro-aniline
99-09-2

3-nitro-aniline

A

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

B

3-Bromonitrobenzene
585-79-5

3-Bromonitrobenzene

Conditions
ConditionsYield
With sulfuric acid; acetic acid Diazotization.Eintragen der Diazoniumsalz-Loesung in eine Loesung von CuCl in wss. HBr;
3-Nitrobenzenesulfonic acid
98-47-5

3-Nitrobenzenesulfonic acid

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With copper dichloride
perfluoro(methylcyclohexane)
355-02-2

perfluoro(methylcyclohexane)

3-Chloronitrobenzene radical anion
34467-54-4, 121-73-3

3-Chloronitrobenzene radical anion

A

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

B

1,1,2,2,3,3,4,4,5,5,6-Undecafluoro-6-trifluoromethyl-cyclohexane
96759-86-3

1,1,2,2,3,3,4,4,5,5,6-Undecafluoro-6-trifluoromethyl-cyclohexane

Conditions
ConditionsYield
In gas at 150℃; Rate constant;
methyl 4-chloro-2-nitrobenzoate
42087-80-9

methyl 4-chloro-2-nitrobenzoate

A

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

B

4-chloro-2-fluorobenzoic acid methyl ester

4-chloro-2-fluorobenzoic acid methyl ester

C

methyl 4-fluoro-2-nitrobenzoate
151504-81-3

methyl 4-fluoro-2-nitrobenzoate

Conditions
ConditionsYield
With potassium fluoride; tetraphenylphosphonium bromide In dimethyl sulfoxide at 130℃; for 27h;A 2.5 % Chromat.
B 72 % Chromat.
C 0.9 % Chromat.
With potassium fluoride; tetraphenylphosphonium bromide In N,N-dimethyl acetamide at 130℃; for 25h;A 2 % Chromat.
B 31 % Chromat.
C 5 % Chromat.
nitrobenzene radical anion
98-95-3, 12169-65-2

nitrobenzene radical anion

3-Chloronitrobenzene radical anion
34467-54-4, 121-73-3

3-Chloronitrobenzene radical anion

A

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

B

nitrobenzene
98-95-3

nitrobenzene

Conditions
ConditionsYield
at 76.9℃; Rate constant;
C7H6ClN3O3
81536-33-6

C7H6ClN3O3

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With methanol; sodium methylate at 10℃; Rate constant;
C8H8ClN3O3
71099-79-1

C8H8ClN3O3

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

Conditions
ConditionsYield
With ethanol; sodium ethanolate at 10℃; Rate constant; var. base concentrations;
methoxybenzene
100-66-3

methoxybenzene

A

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

B

4-chlorobenzonitrile
100-00-5

4-chlorobenzonitrile

C

2-Chloronitrobenzene
88-73-3

2-Chloronitrobenzene

Conditions
ConditionsYield
With N-nitro-2,4,6-trimethylpyridinium tetrafluoroborate In nitromethane at 25℃; Rate constant; competitive nitration with benzene;
nitrobenzene
98-95-3

nitrobenzene

A

3,4-dichloronitrobenzene
99-54-7

3,4-dichloronitrobenzene

B

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

C

1,2-Dichloro-3-nitrobenzene
3209-22-1

1,2-Dichloro-3-nitrobenzene

D

4-chlorobenzonitrile
100-00-5

4-chlorobenzonitrile

E

2-Chloronitrobenzene
88-73-3

2-Chloronitrobenzene

F

2,5-dichloronitrobenzene
89-61-2

2,5-dichloronitrobenzene

Conditions
ConditionsYield
With chlorine; iron(III) chloride at 60 - 120℃; Product distribution; Kinetics; relative rates of each steps;
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

3-chloro-aniline
108-42-9

3-chloro-aniline

Conditions
ConditionsYield
With 2 weight% platinum on carbon; ethanol at 100℃; under 7500.75 Torr; for 8h; Autoclave;100%
With hydrogen In ethanol at 20℃; under 7500.75 Torr; for 8h; Catalytic behavior; Sealed tube;100%
With hydrazine hydrate In ethanol; water at 80℃; for 1h; chemoselective reaction;100%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

potassium isopropoxide
6831-82-9

potassium isopropoxide

3,3'-dichloroazoxybenzene
139-24-2, 71297-98-8

3,3'-dichloroazoxybenzene

Conditions
ConditionsYield
In isopropyl alcohol at 75℃; Mechanism; Product distribution; Rate constant; also with the K+ complexing 18-crown-6 ether under anaerobic and aerobic conditions;100%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

chloromethyl phenyl sulfone
7205-98-3

chloromethyl phenyl sulfone

1-Benzenesulfonylmethyl-2-chloro-4-nitro-benzene
89303-35-5

1-Benzenesulfonylmethyl-2-chloro-4-nitro-benzene

Conditions
ConditionsYield
Stage #1: chloromethyl phenyl sulfone With potassium hydroxide In dimethyl sulfoxide for 0.166667h; Inert atmosphere;
Stage #2: 3-Nitrochlorobenzene In dimethyl sulfoxide at 20℃; for 0.166667h; Inert atmosphere;
100%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

phenylboronic acid
98-80-6

phenylboronic acid

3-nitro-1,1'-biphenyl
2113-58-8

3-nitro-1,1'-biphenyl

Conditions
ConditionsYield
With caesium carbonate; tris(dibenzylideneacetone)dipalladium (0) In 1,4-dioxane for 1h; Suzuki-Miyaura coupling; Heating;99%
With [PdCl{[(η5-C5H5)]Fe[(η5-C5H3)CH=NCy]}(PCy3)]; caesium carbonate In 1,4-dioxane at 100℃; for 12h; Suzuki coupling reaction;98.5%
With (bis(tricyclohexyl)phosphine)palladium(II) dichloride; cesium fluoride In various solvent(s) at 100℃; for 10h;97%
morpholine
110-91-8

morpholine

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

3-morpholinonitrobenzene
116922-22-6

3-morpholinonitrobenzene

Conditions
ConditionsYield
With sodium t-butanolate; palladium diacetate; [(μ-PPh2CH2PPh2)Co2(CO)4][μ,η-PhCCP(tBu)2] In toluene at 60℃; for 4h;99%
With sodium methylate; triethylamine; 2-(di-t-butylphosphino)biphenyl palladium In toluene at 60℃; for 5h;85%
With potassium acetate; 1-butyl-3-methylimidazolium Tetrafluoroborate for 0.0333333h; microwave irradiation;56%
In various solvent(s) at 180℃; for 5h; Irradiation;14%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

cyclohexylamine
108-91-8

cyclohexylamine

N-cyclohexyl-3-nitrobenzenamine
121086-17-7

N-cyclohexyl-3-nitrobenzenamine

Conditions
ConditionsYield
With copper(l) iodide; potassium carbonate In N,N-dimethyl-formamide at 20 - 110℃;99%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

m-tolylboronic acid
17933-03-8

m-tolylboronic acid

3-methyl-3'-nitro-1,1'-biphenyl
952-03-4

3-methyl-3'-nitro-1,1'-biphenyl

Conditions
ConditionsYield
With potassium phosphate tribasic trihydrate; C30H39P; palladium diacetate In tetrahydrofuran at 110℃; for 3h; Suzuki-Miyaura Coupling; Inert atmosphere;99%
With potassium phosphate tribasic trihydrate; (2-(anthracen-9-yl)-1H-inden-3-yl)dicyclohexylphosphine; palladium diacetate In water; isopropyl alcohol; toluene at 90℃; for 16h; Suzuki-Miyaura Coupling; Schlenk technique; Inert atmosphere;94%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

N-(3-chlorophenyl)hydroxylamine
10468-17-4

N-(3-chlorophenyl)hydroxylamine

Conditions
ConditionsYield
With carbon dioxide; zinc In water at 25℃; under 750.075 Torr; for 0.666667h; Sonication;98%
With ammonium formate; zinc In acetonitrile at 25 - 30℃; for 1h; sonification;94%
With hydrazine hydrate at 60℃; for 0.666667h; Green chemistry; chemoselective reaction;87%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

3,3'-dichloroazobenzene
15426-14-9, 106131-20-8, 106131-24-2

3,3'-dichloroazobenzene

Conditions
ConditionsYield
With C24H16CoN4O4; hydrogen; sodium hydroxide In tert-butyl alcohol at 80℃; under 22502.3 Torr; for 1h; chemoselective reaction;98%
With hydrogen In toluene at 50℃; under 15001.5 Torr; for 7h; Autoclave; Green chemistry; chemoselective reaction;97%
Stage #1: 3-Nitrochlorobenzene In ethanol for 0.0333333h;
Stage #2: With sodium tetrahydroborate In ethanol for 0.3h; Reflux;
96%
styrene
292638-84-7

styrene

carbon monoxide
201230-82-2

carbon monoxide

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

N-(3-chlorophenyl)-2-phenylpropanamide
59960-68-8

N-(3-chlorophenyl)-2-phenylpropanamide

Conditions
ConditionsYield
With 1,1'-bis-(diphenylphosphino)ferrocene; potassium tetrachloropalladate(II); boric acid In tetrahydrofuran at 80℃; under 26252.6 Torr; for 20h; Reagent/catalyst; Autoclave; regioselective reaction;98%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

3,4-dinitro-chlorobenzene
610-40-2

3,4-dinitro-chlorobenzene

Conditions
ConditionsYield
With sulfuric acid; nitric acid at 30℃; for 1h;97%
With sulfuric acid; uronium nitrate at 0 - 20℃; Nitration;77%
With sulfuric acid; potassium nitrate
With sulfuric acid; potassium nitrate
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

benzyl alcohol
100-51-6

benzyl alcohol

1-(benzyloxy)-3-chlorobenzene
24318-02-3

1-(benzyloxy)-3-chlorobenzene

Conditions
ConditionsYield
With potassium hydroxide; tetrabutylammomium bromide In various solvent(s) 1) 5 h, room temperature, 2) 3 h, 50 deg C; other nitrobenzene derivatives, other reaction times and temperatures;97%
With potassium hydroxide; tetrabutylammomium bromide In various solvent(s) at 50℃; for 24h;97%
5-Amino-1,3-dimethylpyrazole
3524-32-1

5-Amino-1,3-dimethylpyrazole

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

1,3-dimethyl-N-(3-nitrophenyl)-1H-pyrazol-5-amine
1255920-13-8

1,3-dimethyl-N-(3-nitrophenyl)-1H-pyrazol-5-amine

Conditions
ConditionsYield
With chloro[2-(dicyclohexylphosphino)-3 ,6-dimethoxy-2’,4’, 6’-triisopropyl- 1,1’-biphenyl] [2-(2-aminoethyl)phenyl]palladium(II); caesium carbonate; ruphos In tert-butyl alcohol at 110℃; for 24h; Inert atmosphere;97%
formic acid
64-18-6

formic acid

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

m-chloroformanilide
139-71-9

m-chloroformanilide

Conditions
ConditionsYield
With silver nanoparticles decorated mesoporous 1,3,5-triformylphloroglucinol-DMB covalent organic framework nanomaterial In water at 20℃; for 2h; Catalytic behavior; Irradiation; Green chemistry;97%
With gold nano particles supported on rutile TiO2 In toluene at 70℃; under 750.075 Torr; for 3h; Inert atmosphere; chemoselective reaction;96%
With cobalt nanoparticles anchoring on nitrogen doped carbon, pyrolysis at 700 °C In acetonitrile at 110℃; under 750.075 Torr; for 5h; Inert atmosphere; chemoselective reaction;93.8%
With dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; triethylamine; potassium iodide In dimethyl sulfoxide at 100℃; for 20h; Inert atmosphere; chemoselective reaction;86%
With palladium(II) trifluoroacetate; triphenylphosphine In water at 80℃; for 2.5h; Sealed tube; Green chemistry;77%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

2-Methyl-4-phenyl-3-butyn-2-ol
1719-19-3

2-Methyl-4-phenyl-3-butyn-2-ol

1-(3-nitrophenyl)-2-phenylacetylene
29338-47-4

1-(3-nitrophenyl)-2-phenylacetylene

Conditions
ConditionsYield
With {(Pd{Fe(η5-C5H5)(η5-C5H3C(CH3)=NC6H4CH3-4)}(μ-Cl))2}; potassium carbonate; XPhos In acetonitrile at 110℃; for 16h; Inert atmosphere;96%
With tetrabutylammomium bromide; potassium carbonate; palladium dichloride; XPhos In water at 120℃; Inert atmosphere; Schlenk technique; Green chemistry;87%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

sodium 4-methylbenzenesulfinate
824-79-3

sodium 4-methylbenzenesulfinate

N-(3-chloro-phenyl)-4-methylbenzenesulfonamide
19377-04-9

N-(3-chloro-phenyl)-4-methylbenzenesulfonamide

Conditions
ConditionsYield
With trans-N,N'-dimethyl-1,2-cyclohexyldiamine; sodium hydrogen sulfite; iron(II) chloride In dimethyl sulfoxide at 60℃; for 12h; Sealed tube; Inert atmosphere;96%
Stage #1: 3-Nitrochlorobenzene With tetrahydroxydiboron In methanol; water at 100℃; for 8h; Schlenk technique;
Stage #2: sodium 4-methylbenzenesulfinate With iodine In methanol; water at 35℃; for 3h; Schlenk technique;
80%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

acetic anhydride
108-24-7

acetic anhydride

3-Chloroacetanilide
588-07-8

3-Chloroacetanilide

Conditions
ConditionsYield
With indium; acetic acid In methanol at 20℃; for 1h;95%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

N-(2-bromophenyl)formamide
10113-38-9

N-(2-bromophenyl)formamide

molybdenum hexacarbonyl
13939-06-5, 199620-15-0

molybdenum hexacarbonyl

3-(3-chlorophenyl)-4(3H)-quinazolinone
24122-26-7

3-(3-chlorophenyl)-4(3H)-quinazolinone

Conditions
ConditionsYield
With palladium diacetate; triethylamine In 1,4-dioxane at 140℃; under 7500.75 Torr; for 16h; Inert atmosphere;95%
1-trifluoromethyl-4-vinyl-benzene
402-50-6

1-trifluoromethyl-4-vinyl-benzene

carbon monoxide
201230-82-2

carbon monoxide

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

C16H13ClF3NO

C16H13ClF3NO

Conditions
ConditionsYield
With tetrakis(acetonitrile)palladium bistriflate; boric acid; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene In tetrahydrofuran at 80℃; under 750.075 Torr; for 20h; Autoclave; regioselective reaction;95%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

butan-1-ol
71-36-3

butan-1-ol

n-butyl 3-nitrophenylether
122329-01-5

n-butyl 3-nitrophenylether

Conditions
ConditionsYield
With palladium diacetate; caesium carbonate; 2-N,N-(dimethylamino)-2'-di-tert-butylphosphino-1,1'-binaphthyl In toluene at 70℃;94%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

aniline
62-53-3

aniline

3-nitro-N-phenylaniline
4531-79-7

3-nitro-N-phenylaniline

Conditions
ConditionsYield
With potassium hydroxide; tris(dibenzylideneacetone)dipalladium (0); XPhos In water at 60℃; for 8h;94%
With potassium acetate; 1-butyl-3-methylimidazolium Tetrafluoroborate for 0.0333333h; microwave irradiation;43%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

4-[4-(4-fluorophenyl)-1-methyl-2-methylsulfanyl-1H-imidazol-5-yl]pyridin-2-ylamine
452056-98-3

4-[4-(4-fluorophenyl)-1-methyl-2-methylsulfanyl-1H-imidazol-5-yl]pyridin-2-ylamine

C22H18FN5O2S

C22H18FN5O2S

Conditions
ConditionsYield
With BrettPhos precatalyst; caesium carbonate In 1,4-dioxane; tert-butyl alcohol for 4h; Reagent/catalyst; Solvent; Buchwald-Hartwig Coupling;94%
carbon monoxide
201230-82-2

carbon monoxide

3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

methylenecyclohexane
1192-37-6

methylenecyclohexane

N-(3-chlorophenyl)cyclohexanecarboxamide

N-(3-chlorophenyl)cyclohexanecarboxamide

Conditions
ConditionsYield
With tetrakis(acetonitrile)palladium bistriflate; boric acid; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene In tetrahydrofuran at 80℃; under 750.075 Torr; for 20h; Reagent/catalyst; Autoclave; regioselective reaction;94%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

3,3'-dichloroazoxybenzene
139-24-2, 71297-98-8

3,3'-dichloroazoxybenzene

Conditions
ConditionsYield
With potassium hydroxide In water; isopropyl alcohol at 30℃; under 760.051 Torr; for 8h; Inert atmosphere;93%
With bismuth for 1.5h;92%
With cerium(IV) oxide; hydrogen In toluene at 120℃; under 7500.75 Torr; chemoselective reaction;92%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

acetic anhydride
108-24-7

acetic anhydride

N-(acetyloxy)-N-(3-chlorophenyl) acetamide

N-(acetyloxy)-N-(3-chlorophenyl) acetamide

Conditions
ConditionsYield
With methanol; indium(III) chloride; indium In chloroform at 20℃; for 19h;93%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

toluene
108-88-3

toluene

N-benzyl-3-chloroaniline
50798-95-3

N-benzyl-3-chloroaniline

Conditions
ConditionsYield
With tert.-butylhydroperoxide; hydrogen In water; toluene at 160℃; under 30003 Torr; for 36h; Autoclave;93%
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

(E)-1,2-bis(3-chlorophenyl)diazene
106131-20-8, 15426-14-9, 106131-24-2

(E)-1,2-bis(3-chlorophenyl)diazene

Conditions
ConditionsYield
With isopropyl alcohol; sodium hydroxide at 30℃; for 2h; Catalytic behavior; Inert atmosphere; UV-irradiation;92%
With ammonium acetate; lead In methanol at 20℃;87%
With hydrazine hydrate; potassium hydroxide In toluene at 100℃; for 1h; Sealed tube;85%

3-Nitrochlorobenzene Consensus Reports

Reported in EPA TSCA Inventory.

3-Nitrochlorobenzene Standards and Recommendations

DOT Classification:  6.1; Label: Poison

3-Nitrochlorobenzene Specification

The 3-Nitrochlorobenzene, with the cas registry number 121-73-3, has its systematic name of 1-chloro-3-nitrobenzene. This is a kind of pale yellow crystalline solid and is insoluble in water. Besides, it is stable chemically but incompatible with strong oxidizing agents, strong acids, strong reducing agents. Its product categories are various, including intermediates of dyes and pigments; benzene derivates; alpha sort; analytical standards; aromaticsvolatiles/ semivolatiles; c; calphabetic; chchemical class; chemical class; chloroanalytical standards; halogenated; nitro compounds; nitrogen compounds; organic building blocks.

The characteristics of this chemical are as follows: (1)ACD/LogP: 2.64; (2)ACD/LogD (pH 5.5): 2.64; (3)ACD/LogD (pH 7.4): 2.64; (4)ACD/BCF (pH 5.5): 59.52; (5)ACD/BCF (pH 7.4): 59.52; (6)ACD/KOC (pH 5.5): 648.54; (7)ACD/KOC (pH 7.4): 648.54; (8)#H bond acceptors: 3; (9)#Freely Rotating Bonds: 1; (10)Polar Surface Area: 45.82; (11)Index of Refraction: 1.58; (12)Molar Refractivity: 37.69 cm3; (13)Molar Volume: 113.2 cm3; (14)Polarizability: 14.94 ×10-24 cm3; (15)Surface Tension: 48.3 dyne/cm; (16)Density: 1.391 g/cm3; (17)Flash Point: 103.3 °C; (18)Enthalpy of Vaporization: 45.36 kJ/mol; (19)Boiling Point: 236 °C at 760 mmHg; (20)Vapour Pressure: 0.0744 mmHg at 25°C; (21)Exact Mass: 156.993056; (22)MonoIsotopic Mass: 156.993056; (23)Topological Polar Surface Area: 45.8; (24)Heavy Atom Count: 10; (25)Complexity: 134.

Production method of 3-Nitrochlorobenzene is as below: 1-bromo-3-nitro-benzene could react to produce 3-Nitrochlorobenzene, with the following condition: reagent: LiCl; solvent: H2O and acetic acid; yield: 90%; other condition: Irradiation.

Use of 3-Nitrochlorobenzene: 3-Nitrochlorobenzene reacts to produce N-(3-chloro-phenyl)-hydroxylamine, with the following condition: reagent: KBH4, BiCl3; solvent: aq. ethanol; reaction time: 15 min; yield: 83%; other condition: Ambient temperature.

As to its usage, it is widely applied in many ways. It can be used as raw materials of organic synthesis and dyes' intermediates; It also could be used  for the system of inter-chloro-aniline; Then it can be also used in the pharmaceutical industry.

While dealing with this chemical, you should be very cautious. For one thing, being a kind of harmful chemical, it may cause damage to health, and it is toxic if by inhalation, in contact with skin and if swallowed. For another thing, it is dangerous for the environment. It may present an immediate or delayed danger to one or more components of the environment, and it is very toxic to aquatic organisms, which may cause long-term adverse effects in the aquatic environment.

Therefore, you should take the following instructions. Wear suitable protective clothing, gloves and eye/face protection. Then do not breathe dust and avoid contacting with skin and eyes at the same time. If in case of accident or if you feel unwell seek medical advice immediately (show the label where possible); If in case of insufficient ventilation wear suitable respiratory equipment. While using this chemical, you should also be careful. This material and its container must be disposed of as hazardous waste, and avoid releasing to the environment, with refering to special instructions/safety data sheet.

Additionally, the following datas could be converted into the molecular structure:
SMILES:
O=[N+]([O-])c1cc(Cl)ccc1

 

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