Product Name

  • Name

    3,4-Dinitrochlorobenzene

  • EINECS 210-223-7
  • CAS No. 610-40-2
  • Article Data11
  • CAS DataBase
  • Density 1.619 g/cm3
  • Solubility insoluble in water, soluble in hot ethanol, ethyl ether
  • Melting Point 40-41 ºC
  • Formula C6H3ClN2O4
  • Boiling Point 335.1 °C at 760 mmHg
  • Molecular Weight 202.554
  • Flash Point 156.5 °C
  • Transport Information UN 3441
  • Appearance yellow liquid or needle-like crystals
  • Safety 28-36/37-45-60-61
  • Risk Codes 23/24/25-33-50/53
  • Molecular Structure Molecular Structure of 610-40-2 (3,4-Dinitrochlorobenzene)
  • Hazard Symbols ToxicT,DangerousN
  • Synonyms 1,2-Dinitro-4-chlorobenzene;1-Chloro-3,4-dinitrobenzene;3,4-Dinitrochlorobenzene;4-Chloro-1,2-dinitrobenzene;NSC 119343;
  • PSA 91.64000
  • LogP 3.20280

Synthetic route

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
4-Chloro-2-nitroaniline
89-63-4

4-Chloro-2-nitroaniline

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

3,4-dinitro-chlorobenzene

Conditions
ConditionsYield
With sulfuric acid; acetic acid; tetra-n-propylammonium bromate for 1.5h; Heating;86%
3,4-dinitroaniline
610-41-3

3,4-dinitroaniline

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

3,4-dinitro-chlorobenzene

Conditions
ConditionsYield
With phosphonic Acid; nitrosylsulfuric acid; sulfuric acid Diazotization.Behandlung der Diazoniumsalz-Loesung mit CuCl in konz. wss. HCl;
2-Chloronitrobenzene
88-73-3

2-Chloronitrobenzene

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

3,4-dinitro-chlorobenzene

Conditions
ConditionsYield
durch Nitrieren;
3,4-dinitophenol
577-71-9

3,4-dinitophenol

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

3,4-dinitro-chlorobenzene

Conditions
ConditionsYield
With trichlorophosphate In N,N-dimethyl-formamide for 2h; Ambient temperature;
α-form

α-form

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

3,4-dinitro-chlorobenzene

Conditions
ConditionsYield
at 39 - 40℃; (Herstellung der β-Form);
β-form

β-form

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

3,4-dinitro-chlorobenzene

Conditions
ConditionsYield
at 42℃; (Herstellung der fluessigen Form);
3-Chloronitrobenzene
121-73-3

3-Chloronitrobenzene

sulfuric acid
7664-93-9

sulfuric acid

nitric acid
7697-37-2

nitric acid

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

3,4-dinitro-chlorobenzene

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

3,4-dinitro-chlorobenzene

4-Chloro-1,2-phenylenediamine
95-83-0

4-Chloro-1,2-phenylenediamine

Conditions
ConditionsYield
With sodium tetrahydroborate; C16H18Cl2N4O2Pd In water at 27℃; for 0.25h;99%
With hydrogenchloride; tin
With sodium tetrahydroborate In water at 20℃; for 40h;
3,4-dinitro-chlorobenzene
610-40-2

3,4-dinitro-chlorobenzene

1,2-bis(4-methoxyphenyl)-1,2-ethanedione
1226-42-2

1,2-bis(4-methoxyphenyl)-1,2-ethanedione

6-chloro-2,3-bis(4-methoxyphenyl)quinoxaline

6-chloro-2,3-bis(4-methoxyphenyl)quinoxaline

Conditions
ConditionsYield
With tin(ll) chloride In ethanol; water for 4h; Reflux;98%
formic acid
64-18-6

formic acid

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

3,4-dinitro-chlorobenzene

5-chloro-1H-benzimidazole
4887-82-5

5-chloro-1H-benzimidazole

Conditions
ConditionsYield
With gold nano particles supported on rutile TiO2 In toluene at 70℃; under 750.075 Torr; for 6h; Inert atmosphere; chemoselective reaction;95%
4,4'-dibromobenzil
35578-47-3

4,4'-dibromobenzil

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

3,4-dinitro-chlorobenzene

2,3-bis(4-bromophenyl)-6-chloroquinoxaline
1094618-65-1

2,3-bis(4-bromophenyl)-6-chloroquinoxaline

Conditions
ConditionsYield
With tin(ll) chloride In ethanol; water for 4h; Reflux;94%
furil
492-94-4

furil

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

3,4-dinitro-chlorobenzene

6-chloro-2,3-di(furan-2-yl)-quinoxaline
70976-04-4

6-chloro-2,3-di(furan-2-yl)-quinoxaline

Conditions
ConditionsYield
With tin(ll) chloride In ethanol; water for 4h; Reflux;94%
3,4-dinitro-chlorobenzene
610-40-2

3,4-dinitro-chlorobenzene

benzil
134-81-6

benzil

2,3-diphenyl-6-chloroquinoxaline
36305-60-9

2,3-diphenyl-6-chloroquinoxaline

Conditions
ConditionsYield
With tin(ll) chloride In ethanol; water for 4h; Reflux;94%
3,4-dinitro-chlorobenzene
610-40-2

3,4-dinitro-chlorobenzene

phenylacetylene
536-74-3

phenylacetylene

1,2-Dinitro-4-phenylethynyl-benzene

1,2-Dinitro-4-phenylethynyl-benzene

Conditions
ConditionsYield
With potassium carbonate; bis(η3-allyl-μ-chloropalladium(II)); (1RS,2RS,3SR,4SR)-1,2,3,4-tetrakis((diphenylphosphanyl)methyl)cyclopentane In N,N-dimethyl-formamide at 140℃; for 20h; Sonogashira cross-coupling;93%
3,4-dinitro-chlorobenzene
610-40-2

3,4-dinitro-chlorobenzene

aniline
62-53-3

aniline

5-chloro-2-nitro-N-phenylaniline
25781-92-4

5-chloro-2-nitro-N-phenylaniline

Conditions
ConditionsYield
In ethanol at 20℃; for 10h; Solvent; Temperature; Time;90%
3,4-dinitro-chlorobenzene
610-40-2

3,4-dinitro-chlorobenzene

4-Chloro-2-nitroaniline
89-63-4

4-Chloro-2-nitroaniline

Conditions
ConditionsYield
With sodium tetrahydroborate In ethanol; water at 20℃; for 4h; Green chemistry;90%
ethanol
64-17-5

ethanol

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

3,4-dinitro-chlorobenzene

6-chloro-2-methyl-1H-benzo[d]imidazole
2818-69-1

6-chloro-2-methyl-1H-benzo[d]imidazole

Conditions
ConditionsYield
With titanium(IV) oxide for 4h; Irradiation;89%
3,4-dinitro-chlorobenzene
610-40-2

3,4-dinitro-chlorobenzene

1,2-diamino-benzene
95-54-5

1,2-diamino-benzene

Conditions
ConditionsYield
With palladium 10% on activated carbon; hydrazine hydrate In methanol at 120℃; for 0.25h; Microwave irradiation;89%
3,4-dinitro-chlorobenzene
610-40-2

3,4-dinitro-chlorobenzene

1,2,4-Trichlorobenzene
120-82-1

1,2,4-Trichlorobenzene

Conditions
ConditionsYield
With Dichlorophenylphosphine In various solvent(s) at 170℃; for 5h;86%
cyclohexylamine
108-91-8

cyclohexylamine

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

3,4-dinitro-chlorobenzene

N-cyclohexyl-2-nitro-5-chloro-aniline
28096-58-4

N-cyclohexyl-2-nitro-5-chloro-aniline

Conditions
ConditionsYield
In ethanol for 8h; Ambient temperature;85%
propan-1-ol
71-23-8

propan-1-ol

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

3,4-dinitro-chlorobenzene

6-chloro-2-ethylbenzimidazole

6-chloro-2-ethylbenzimidazole

Conditions
ConditionsYield
With titanium(IV) oxide for 4h; Irradiation;84%
3,4-dinitro-chlorobenzene
610-40-2

3,4-dinitro-chlorobenzene

triethyl phosphite
122-52-1

triethyl phosphite

C10H13N2O7P

C10H13N2O7P

Conditions
ConditionsYield
In toluene Michaelis-Arbuzov Synthesis; Reflux;84%
3,4-dinitro-chlorobenzene
610-40-2

3,4-dinitro-chlorobenzene

toluene-4-sulfonic acid hydrazide
1576-35-8

toluene-4-sulfonic acid hydrazide

3,4-dinitro-1-(4-methylphenylsulfonyl)-benzene
127291-62-7

3,4-dinitro-1-(4-methylphenylsulfonyl)-benzene

Conditions
ConditionsYield
With sodium acetate In ethanol for 1h; Heating;80%
3,4-dinitro-chlorobenzene
610-40-2

3,4-dinitro-chlorobenzene

5-chloro-2-nitrophenylhydrazine
1966-16-1

5-chloro-2-nitrophenylhydrazine

Conditions
ConditionsYield
With hydrazine hydrate; urea In ethanol76%
With hydrazine In ethanol at 20℃; for 1h;62%
With hydrazine hydrate
With ethanol; hydrazine hydrate
4-phenyl-butan-1-ol
3360-41-6

4-phenyl-butan-1-ol

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

3,4-dinitro-chlorobenzene

4-(4-phenylbutoxy)-1,2-dinitrobenzene

4-(4-phenylbutoxy)-1,2-dinitrobenzene

Conditions
ConditionsYield
In tetrahydrofuran; mineral oil72%
(2R)-methylpiperazine
75336-86-6

(2R)-methylpiperazine

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

3,4-dinitro-chlorobenzene

A

(R)-1-(3,4-Dinitro-phenyl)-3-methyl-piperazine

(R)-1-(3,4-Dinitro-phenyl)-3-methyl-piperazine

B

(R)-1-(5-chloro-2-nitrophenyl)-3-methylpiperazine
907991-13-3

(R)-1-(5-chloro-2-nitrophenyl)-3-methylpiperazine

Conditions
ConditionsYield
With potassium carbonate In ethanol; water for 1h; Heating;A n/a
B 71%
pyrrolidine
123-75-1

pyrrolidine

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

3,4-dinitro-chlorobenzene

A

4-chloro-2-(1-pyrrolidinyl)nitrobenzene
133387-30-1

4-chloro-2-(1-pyrrolidinyl)nitrobenzene

B

1-(3,4-dinitro-phenyl)-pyrrolidine

1-(3,4-dinitro-phenyl)-pyrrolidine

Conditions
ConditionsYield
In methanol at 20℃; for 5h;A 70%
B n/a
3,4-dinitro-chlorobenzene
610-40-2

3,4-dinitro-chlorobenzene

benzylamine
100-46-9

benzylamine

A

N-benzyl-N-(2-nitro-5-chlorophenyl)-amine
10066-19-0

N-benzyl-N-(2-nitro-5-chlorophenyl)-amine

B

N-Benzyl-2,4-dinitroanilin

N-Benzyl-2,4-dinitroanilin

Conditions
ConditionsYield
In methanol at 20℃; for 3h;A 70%
B n/a
3,4-dinitro-chlorobenzene
610-40-2

3,4-dinitro-chlorobenzene

rac-methylbenzylamine
618-36-0

rac-methylbenzylamine

A

N-(1-phenylethyl)-5-chloro-2-nitroaniline
330830-31-4

N-(1-phenylethyl)-5-chloro-2-nitroaniline

B

(3,4-dinitro-phenyl)-(1-phenyl-ethyl)-amine

(3,4-dinitro-phenyl)-(1-phenyl-ethyl)-amine

Conditions
ConditionsYield
In methanol at 20℃; for 3h;A 68%
B n/a
piperidine
110-89-4

piperidine

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

3,4-dinitro-chlorobenzene

A

1-(5-chloro-2-nitrophenyl)piperidine
53013-43-7

1-(5-chloro-2-nitrophenyl)piperidine

B

1-(3,4-Dinitro-phenyl)-piperidine

1-(3,4-Dinitro-phenyl)-piperidine

Conditions
ConditionsYield
In methanol at 20℃; for 5h;A 65%
B n/a
ethanolamine
141-43-5

ethanolamine

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

3,4-dinitro-chlorobenzene

A

2-<(5-chloro-2-nitro)phenylamino>ethanol
50610-29-2

2-<(5-chloro-2-nitro)phenylamino>ethanol

B

2-(3,4-dinitro-phenylamino)-ethanol

2-(3,4-dinitro-phenylamino)-ethanol

Conditions
ConditionsYield
In methanol at 20℃; for 3h;A 65%
B n/a
2,2-dimethylpropylamine
5813-64-9

2,2-dimethylpropylamine

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

3,4-dinitro-chlorobenzene

A

N-(2,2-dimethylpropyl)-5-chloro-2-nitroaniline
725705-48-6

N-(2,2-dimethylpropyl)-5-chloro-2-nitroaniline

B

(2,2-dimethyl-propyl)-(3,4-dinitro-phenyl)-amine

(2,2-dimethyl-propyl)-(3,4-dinitro-phenyl)-amine

Conditions
ConditionsYield
In methanol at 20℃; for 3h;A 65%
B n/a
3,4-dinitro-chlorobenzene
610-40-2

3,4-dinitro-chlorobenzene

(4-aminophenyl)-α-D-glucopyranoside
31302-52-0

(4-aminophenyl)-α-D-glucopyranoside

4-(3,4-dinitrophenylamino)phenyl α-D-glucopyranoside

4-(3,4-dinitrophenylamino)phenyl α-D-glucopyranoside

Conditions
ConditionsYield
With sodium hydrogencarbonate In ethanol; water for 1h;63%
1-(para-methoxyphenyl)piperazine hydrochloride
84145-43-7

1-(para-methoxyphenyl)piperazine hydrochloride

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

3,4-dinitro-chlorobenzene

1-(5-chloro-2-nitrophenyl)-4-(4-methoxyphenyl)piperazine
150916-81-7

1-(5-chloro-2-nitrophenyl)-4-(4-methoxyphenyl)piperazine

Conditions
ConditionsYield
With potassium carbonate In ethanol; water for 5h; Heating;62%
3,4-dinitro-chlorobenzene
610-40-2

3,4-dinitro-chlorobenzene

triethyl phosphite
122-52-1

triethyl phosphite

O,O-diethyl-5-chloro-2-nitrophenylphosphonate

O,O-diethyl-5-chloro-2-nitrophenylphosphonate

Conditions
ConditionsYield
In toluene for 6h; Heating;60.3%

3,4-Dinitrochlorobenzene Specification

The Benzene,4-chloro-1,2-dinitro-, with the CAS registry number 610-40-2, is also known as 3,4-Dinitrochlorobenzene. It belongs to the product categories of Benzene derivates; API intermediates. Its EINECS number is 210-223-7. This chemical's molecular formula is C6H3ClN2O4 and formula weight is 202.55. What's more, its IUPAC name is 4-chloro-1,2-dinitrobenzene.

Physical properties of Benzene,4-chloro-1,2-dinitro- are: (1)ACD/LogP: 2.58; (2)ACD/LogD (pH 5.5): 2.58; (3)ACD/LogD (pH 7.4): 2.58; (4)ACD/BCF (pH 5.5): 53.99; (5)ACD/BCF (pH 7.4): 53.99; (6)ACD/KOC (pH 5.5): 604.8; (7)ACD/KOC (pH 7.4): 604.8; (8)#H bond acceptors: 6; (9)#H bond donors: 0; (10)#Freely Rotating Bonds: 2; (11)Polar Surface Area: 91.64 Å2; (12)Index of Refraction: 1.625; (13)Molar Refractivity: 44.23 cm3; (14)Molar Volume: 125 cm3; (15)Surface Tension: 64.2 dyne/cm; (16)Density: 1.619 g/cm3; (17)Flash Point: 156.5 °C; (18)Enthalpy of Vaporization: 55.52 kJ/mol; (19)Boiling Point: 335.1 °C at 760 mmHg; (20)Vapour Pressure: 0.000237 mmHg at 25°C.

Uses of Benzene,4-chloro-1,2-dinitro-: it can be used to produce N-cyclohexyl-2-nitro-5-chloro-aniline at the ambient temperature. It will need solvent ethanol with the reaction time of 8 hours. The yield is about 85%.

When you are using this chemical, please be cautious about it as the following:
It is toxic by inhalation, in contact with skin and if swallowed. It is danger of cumulative effects. It is very toxic to aquatic organisms, and may cause long-term adverse effects in the aquatic environment. After contact with skin, you should wash immediately with plenty of ... (to be specified by the manufacturer). When using it, you must wear suitable protective clothing and gloves. In case of accident or if you feel unwell seek medical advice immediately (show the label where possible). This material and its container must be disposed of as hazardous waste. This chemical should avoid release to the environment. You need refer to special instructions/safety data sheet.

You can still convert the following datas into molecular structure:
(1)Canonical SMILES: C1=CC(=C(C=C1Cl)[N+](=O)[O-])[N+](=O)[O-]
(2)InChI: InChI=1S/C6H3ClN2O4/c7-4-1-2-5(8(10)11)6(3-4)9(12)13/h1-3H
(3)InChIKey: QVQSOXMXXFZAKU-UHFFFAOYSA-N

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