4-Chloro-2-nitrophenol supplier

Name
4-CHLORO-2-NITROPHENOL
EINECS 201-927-5
CAS No. 89-64-5
Article Data138
CAS DataBase
Density 1.554 g/cm³
Solubility insoluble in water
Melting Point 85-87 °C
Formula C₆H₄ClNO₃
Boiling Point 242.5 °C at 760 mmHg
Molecular Weight 173.556
Flash Point 100.4 °C
Transport Information UN 2811
Appearance yellow powder
Safety 26-36-36/37/39
Risk Codes 36/37/38-20/21/22
Molecular Structure
Hazard Symbols Xi,Xn
Synonyms 2-Nitro-4-chlorophenol;4-Chloro-2-nitrophenol;4-Chloro-6-nitrophenol;5-Chloro-2-hydroxynitrobenzene;NSC 520345;p-Chloro-o-nitrophenol;4- Chloro -2- Nitrophenol;
PSA 66.05000
LogP 2.47700

Synthetic route

: 106-48-9
4-chloro-phenol

: 89-64-5
p-chloro-o-nitrophenol

Conditions

Conditions	Yield
With dinitrogen tetraoxide; ferric nitrate In acetone Ambient temperature;	99%
With trichloroisocyanuric acid; silica gel; sodium nitrite In dichloromethane at 20℃; for 0.25h;	99%
With 1,3,5-tribromo-1,3,5-triazinane-2,4,6-trione; silica gel; sodium nitrite In dichloromethane at 20℃; for 0.25h;	99%

: 623-12-1
4-chloromethoxybenzene

A: 89-21-4
4-chloro-2-nitroanisole

B: 89-64-5
p-chloro-o-nitrophenol

Conditions

Conditions	Yield
With nitric acid In sulfuric acid at 25℃;	A 98.9% B 0.6%

: 33696-00-3
4-bromo-1-methoxy-2-nitrobenzene

A: 7693-52-9
4-bromo-2-nitrophenol

B: 89-64-5
p-chloro-o-nitrophenol

Conditions

Conditions	Yield
With lithium chloride In N,N-dimethyl-formamide for 4h; Heating;	A 95% B n/a

: 88-75-5
2-hydroxynitrobenzene

: 89-64-5
p-chloro-o-nitrophenol

Conditions

Conditions	Yield
With sodium periodate; sulfuric acid; sodium dodecyl-sulfate; acetic acid; sodium chloride In water at 25℃; for 2h;	85%
Stage #1: 2-hydroxynitrobenzene In acetonitrile at 80℃; for 0.166667h; Stage #2: With N-chloro-succinimide In acetonitrile at 80℃; for 8h; regioselective reaction;	80%
beim Chlorieren;

: 623-12-1
4-chloromethoxybenzene

A: 89-21-4
4-chloro-2-nitroanisole

B: 89-64-5
p-chloro-o-nitrophenol

C: 106-48-9
4-chloro-phenol

Conditions

Conditions	Yield
With nitric acid In sulfuric acid at 25℃; Rate constant; Product distribution; various acid concentrations, molar ratios;	A 83.4% B 17.5% C 5.4%
With nitric acid In sulfuric acid at 25℃;	A 65.4% B 28% C 9.2%

...Expand

: 106-48-9
4-chloro-phenol

A: 89-64-5
p-chloro-o-nitrophenol

B: 123871-57-8
4-chloro-4-nitrocyclohexa-2,5-dienone

Conditions

Conditions	Yield
With nitric acid In chloroform at -60℃; for 0.25h; Title compound not separated from byproducts;	A 20% B 80%
With nitric acid; trifluoroacetic anhydride In diethyl ether at -78℃; for 1.5h;	A 66% B 9%

: 121-73-3
3-Chloronitrobenzene

A: 619-08-9
2-chloro-4-nitrophenol

B: 89-64-5
p-chloro-o-nitrophenol

C: 603-86-1
2-chloro-6-nitrophenol

Conditions

Conditions	Yield
With tert.-butylhydroperoxide; potassium tert-butylate; ammonia In tetrahydrofuran for 0.25h;	A 79% B 1% C 3%
With potassium hydroxide; oxygen In ammonia at -35 - -33℃; for 5h; Product distribution; Mechanism;	A .66 g B n/a C n/a
With Cumene hydroperoxide; potassium tert-butylate In ammonia at -33℃; for 0.25h; Yield given. Yields of byproduct given;

...Expand

: 540-80-7
tert.-butylnitrite

: 106-48-9
4-chloro-phenol

: 89-64-5
p-chloro-o-nitrophenol

Conditions

Conditions	Yield
With water In tetrahydrofuran at 25℃; for 2.5h; Schlenk technique;	62%

: 92044-52-5
1-(benzyloxy)-4-chloro-2-nitrobenzene

A: 1019-90-5
5-chloro-2-phenyl-1,3-benzoxazole

B: 89-64-5
p-chloro-o-nitrophenol

C: 37593-94-5
4-chloro-2-nitrophenyl benzoate

D: 3743-12-2
N-(4-chloro-2-hydroxyphenyl)benzamide

Conditions

Conditions	Yield
In isopropyl alcohol for 10h; Irradiation;	A 3% B 2% C 2% D 50%
In isopropyl alcohol for 10h; Product distribution; Mechanism; Irradiation;	A 3% B 3% C 2% D 50%

...Expand

: 93099-44-6
4-chloro-2-nitrophenyl 4-methylbenzylether

A: 89-64-5
p-chloro-o-nitrophenol

B: N-(4-methylbenzoyl)-2-amino-4-chloro-phenol

C: 16715-75-6
2-(4-methylphenyl)-5-chlorobenzoxazole

Conditions

Conditions	Yield
In isopropyl alcohol for 11h; Irradiation;	A 3% B 41% C 4%
In isopropyl alcohol for 11h; Product distribution; Mechanism; Irradiation;	A 3% B 41% C 4%

...Expand

: 88-75-5
2-hydroxynitrobenzene

A: 89-64-5
p-chloro-o-nitrophenol

B: 609-89-2
2,4-dichloro-6-nitrophenol

C: 603-86-1
2-chloro-6-nitrophenol

Conditions

Conditions	Yield
With oxone; potassium chloride In acetonitrile at 20℃; for 48h;	A 39% B 18% C 6%

...Expand

: 81191-50-6, 61721-88-8
bis(4-chloro-1,2-benzoquinone 2-oximato)copper(II)

: 89-64-5
p-chloro-o-nitrophenol

Conditions

Conditions	Yield
With polymer-supported thiourea In acetone at 20℃; for 24h; Molecular sieve; Inert atmosphere;	5%

: 67-56-1
methanol

: 4-chlorophenyldiazonium nitrate

: 89-64-5
p-chloro-o-nitrophenol

: 64-17-5
ethanol

: 4-chlorophenyldiazonium nitrate

A: 622-61-7
1-chloro-4-ethoxybenzene

B: 89-64-5
p-chloro-o-nitrophenol

C: 108-90-7
chlorobenzene

...Expand

: 91-23-6
2-Nitroanisole

: 89-64-5
p-chloro-o-nitrophenol

Conditions

Conditions	Yield
With aluminium trichloride; sulfuryl dichloride

: 364-76-1
4-Fluoro-3-nitroaniline

A: 89-64-5
p-chloro-o-nitrophenol

B: 345-18-6
2-fluoro-5-chloronitrobenzene

Conditions

Conditions	Yield
und Zersetzen mit Kupfer und wss.HCl.Diazotization;

: 345-18-6
2-fluoro-5-chloronitrobenzene

: 89-64-5
p-chloro-o-nitrophenol

Conditions

Conditions	Yield
With sodium hydroxide

: 60569-15-5
3-nitro-4-propoxy-aniline

: 89-64-5
p-chloro-o-nitrophenol

Conditions

Conditions	Yield
With hydrogenchloride Diazotization.Behandlung mit CuCl in wss. HCl, zuletzt bei 60grad, und Kochen des Reaktionsprodukts mit AlCl3 in Benzol;

: 4-chloro-2-nitro-benzenesulfonic acid

: furan-2,3,5(4H)-trione pyridine (1:1)

: 89-64-5
p-chloro-o-nitrophenol

: 4-amino-2,3-dinitro-phenol

: 89-64-5
p-chloro-o-nitrophenol

Conditions

Conditions	Yield
With Nitrite; acetic acid Diazotization.man kocht das Produkt mit CuCl;

: 106-47-8
4-chloro-aniline

: 89-64-5
p-chloro-o-nitrophenol

Conditions

Conditions	Yield
With sulfuric acid at 5℃; Diazotization.Erwaermen der Diazoniumsalz-Loesung mit wss. HNO3;

: 4-amino-2,3-dinitro-phenol

: 64-19-7
acetic acid

: 89-64-5
p-chloro-o-nitrophenol

Conditions

Conditions	Yield
bei der Zers. der bei Abwesenheit von Mineralsaeure gewonnenen Diazoverbindung mit CuCl;

: 108-90-7
chlorobenzene

: 89-64-5
p-chloro-o-nitrophenol

Conditions

Conditions	Yield
With hydrogenchloride; dihydrogen peroxide; sodium nitrite

: 88-75-5
2-hydroxynitrobenzene

A: 89-64-5
p-chloro-o-nitrophenol

B: 603-86-1
2-chloro-6-nitrophenol

Conditions

Conditions	Yield
With methanol; chlorine

: 89-61-2
2,5-dichloronitrobenzene

: 89-64-5
p-chloro-o-nitrophenol

Conditions

Conditions	Yield
With sodium hydroxide
With potassium carbonate
With sodium hydroxide In water at 120 - 150℃; Autoclave;

: 576-26-1
2.6-dimethylphenol

: 123871-57-8
4-chloro-4-nitrocyclohexa-2,5-dienone

A: 2423-71-4
2,6-dimethyl-4-nitro phenol

B: 89-64-5
p-chloro-o-nitrophenol

C: 106-48-9
4-chloro-phenol

Conditions

Conditions	Yield
In chloroform-d1; chloroform -60 deg C to rt; Yield given. Yields of byproduct given;

...Expand

: 509-14-8
tetranitromethane

: 623-12-1
4-chloromethoxybenzene

A: 89-21-4
4-chloro-2-nitroanisole

B: 89-64-5
p-chloro-o-nitrophenol

C: 88-87-9
4-chloro-2,6-dinitrophenol

D: 110175-20-7
4-chloro-2-(trinitromethyl)anisole

: cis-4-chloro-5-hydroxy-2-trinitromethylanisole

: cis-4-chloro-2-trinitromethyl-5-nitritoanisole

Conditions

Conditions	Yield
In dichloromethane Product distribution; Irradiation; var. solvent, var.temperature;

...Expand

: 121-73-3
3-Chloronitrobenzene

A: 619-08-9
2-chloro-4-nitrophenol

B: 89-64-5
p-chloro-o-nitrophenol

C: 603-86-1
2-chloro-6-nitrophenol

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

Conditions

Conditions	Yield
With potassium hydroxide In ammonia at -35 - -33℃; for 5h; Product distribution; Mechanism;	A .34 g B n/a C n/a D .19 g

...Expand

: 3229-70-7
phenolate

: 4-chloro-2-nitrophenyl 4-nitrobenzenesulfonate

A: 89-64-5
p-chloro-o-nitrophenol

B: 32337-46-5
Phenyl p-nitrobenzenesulphonate

Conditions

Conditions	Yield
With potassium chloride In 1,4-dioxane; water at 50℃; Rate constant;

...Expand

: 68797-94-4
1-acetoxy-6-bromohexane

: 89-64-5
p-chloro-o-nitrophenol

: 892413-80-8
6-(4-chloro-2-nitrophenoxy)-1-hexanol acetate ester

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl acetamide at 60 - 90℃;	100%

: 89-64-5
p-chloro-o-nitrophenol

: 95-85-2
2-hydroxy-5-chloro-aniline

Conditions

Conditions	Yield
With hydrazine hydrate In water at 110℃; Sealed tube; Green chemistry;	99%
With hydrazine hydrate In ethanol at 70℃; for 0.133333h;	96%
With hydrazine hydrate In isopropyl alcohol at 110℃; for 0.2h; Catalytic behavior; Sealed tube; chemoselective reaction;	94%

: 89-64-5
p-chloro-o-nitrophenol

: 533-68-6
2-bromobutyric acid ethyl ester

: 57463-15-7
2-(4-chloro-2-nitro-phenoxy)-butyric acid ethyl ester

Conditions

Conditions	Yield
Stage #1: p-chloro-o-nitrophenol With potassium hydroxide In ethanol for 1h; Stage #2: 2-bromobutyric acid ethyl ester In N,N-dimethyl-formamide for 24h; Inert atmosphere;	99%
With potassium carbonate In acetone for 48h; Heating;

: 89-64-5
p-chloro-o-nitrophenol

: 105-36-2
ethyl bromoacetate

: 344443-67-0
ethyl 4-chloro-2-nitrophenoxyacetate

Conditions

Conditions	Yield
Stage #1: p-chloro-o-nitrophenol With potassium hydroxide In ethanol for 1h; Stage #2: ethyl bromoacetate In N,N-dimethyl-formamide for 24h; Further stages.;	99%
Stage #1: p-chloro-o-nitrophenol With potassium hydroxide In ethanol for 1h; Stage #2: ethyl bromoacetate In N,N-dimethyl-formamide for 24h; Inert atmosphere;	99%
With tetrabutylammomium bromide; potassium carbonate In acetone at 50℃; for 2h;	91%
With potassium carbonate; potassium iodide In acetonitrile at 80℃; for 2h;

: 615-83-8
2-bromo-pentanoic acid ethyl ester

: 89-64-5
p-chloro-o-nitrophenol

: 1225014-17-4
C13H16ClNO5

Conditions

Conditions	Yield
Stage #1: p-chloro-o-nitrophenol With potassium hydroxide In ethanol for 1h; Stage #2: 2-bromo-pentanoic acid ethyl ester In N,N-dimethyl-formamide for 24h; Inert atmosphere;	99%

: 89-64-5
p-chloro-o-nitrophenol

: 2882-19-1
ethyl 2-phenyl-2-bromoacetate

: 1225014-18-5
C16H14ClNO5

Conditions

Conditions	Yield
Stage #1: p-chloro-o-nitrophenol With potassium hydroxide In ethanol for 1h; Stage #2: ethyl 2-phenyl-2-bromoacetate In N,N-dimethyl-formamide for 24h; Inert atmosphere;	99%

: 89-64-5
p-chloro-o-nitrophenol

: 100-07-2
4-methoxy-benzoyl chloride

: 1290636-90-6
C14H10ClNO5

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 20℃; for 1h;	98%
With triethylamine In diethyl ether
With triethylamine In diethyl ether

: 89-64-5
p-chloro-o-nitrophenol

: potassium salt of 4-chloro-2-nitrophenol

Conditions

Conditions	Yield
With potassium hydroxide In dichloromethane; water	98%

: 50-00-0
formaldehyd

: 89-64-5
p-chloro-o-nitrophenol

: 626-56-2, 53152-98-0
3-Methylpiperidine

: 157831-70-4
4-chloro-6-(3'-methylpiperidin-1'-ylmethyl)-2-nitrophenol

Conditions

Conditions	Yield
In ethanol at 97℃; Heating;	97%

...Expand

: 89-64-5
p-chloro-o-nitrophenol

: 106-95-6
allyl bromide

: 100246-31-9
1-(allyloxy)-4-chloro-2-nitrobenzene

Conditions

Conditions	Yield
With potassium carbonate In acetonitrile at 70℃; for 24h; Schlenk technique;	97%
With potassium carbonate In acetone for 6h; Heating;

: 89-64-5
p-chloro-o-nitrophenol

: 75-26-3
isopropyl bromide

: 692284-82-5
4-chloro-2-isopropoxynitrobenzene

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 75 - 80℃; for 6h;	97%

: 89-64-5
p-chloro-o-nitrophenol

: 98-88-4
benzoyl chloride

: 37593-94-5
4-chloro-2-nitrophenyl benzoate

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 20℃; for 1h;	97%
With triethylamine In diethyl ether
With triethylamine In diethyl ether
With triethylamine In diethyl ether

: 2417-73-4
methyl 2-bromomethylbenzoate

: 89-64-5
p-chloro-o-nitrophenol

: 1451261-90-7
methyl 2-((4-chloro-2-nitrophenoxy)methyl)benzoate

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 16h;	96%

: 89-64-5
p-chloro-o-nitrophenol

: 1129-28-8
3-methoxycarbonylbenzyl bromide

: 1451261-96-3
methyl 3-((4-chloro-2-nitrophenoxy)methyl)benzoate

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 16h;	96%

: 89-64-5
p-chloro-o-nitrophenol

: 15969-10-5
2-bromo-4-chloro-6-nitro-phenol

Conditions

Conditions	Yield
With bromine In water at 20℃; for 0.166667h;	95%
With bromine; acetic acid at 5 - 20℃;	90.9%
With bromine; acetic acid at 5 - 20℃; for 3.5h;	84%
With bromine; acetic acid at 20℃; for 4h; Cooling with ice;	76%
With bromine; acetic acid

: 89-64-5
p-chloro-o-nitrophenol

: 870-63-3
prenyl bromide

: 4-chloro-1-(3'-methylbut-2'-enyloxy)-2-nitrobenzene

Conditions

Conditions	Yield
With potassium carbonate In acetone Heating;	95%

: 89-64-5
p-chloro-o-nitrophenol

: 100-51-6
benzyl alcohol

: 1019-90-5
5-chloro-2-phenyl-1,3-benzoxazole

Conditions

Conditions	Yield
With Au NCs/TiO2 In toluene at 130℃; for 24h; Inert atmosphere;	95%
With 1,1'-bis-(diphenylphosphino)ferrocene In toluene at 150℃; for 24h; Inert atmosphere;	80%

: 50-00-0
formaldehyd

: 89-64-5
p-chloro-o-nitrophenol

: 124-40-3
dimethyl amine

: 157831-66-8
4-chloro-6-(dimethylaminomethyl)-2-nitrophenol

Conditions

Conditions	Yield
In ethanol at 97℃; Heating;	94%

...Expand

: 89-64-5
p-chloro-o-nitrophenol

: 100-39-0
benzyl bromide

: 92044-52-5
1-(benzyloxy)-4-chloro-2-nitrobenzene

Conditions

Conditions	Yield
With potassium carbonate In DMF (N,N-dimethyl-formamide) at 60℃; for 22h;	94%
With potassium carbonate In N,N-dimethyl-formamide at 20℃;

: (2R,5S)-5-chloro-2-{2-[4-(4-fluoro-benzyl)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-benzoic acid methyl ester

: 89-64-5
p-chloro-o-nitrophenol

: (2R,5S)-2-(4-chloro-2-nitro-phenoxy)-1-[4-(4-fluoro-benzyl)-2,5-dimethyl-piperazin-1-yl]-ethanone

Conditions

Conditions	Yield
With potassium iodide; potassium carbonate In butanone	93%

: 89-64-5
p-chloro-o-nitrophenol

: 56-81-5
glycerol

: 95-85-2
2-hydroxy-5-chloro-aniline

: 25395-13-5
5-chloro-8-hydroxyquinoline hydrochloride

Conditions

Conditions	Yield
Stage #1: p-chloro-o-nitrophenol; glycerol; 2-hydroxy-5-chloro-aniline With sulfuric acid; boric acid In water at 120℃; for 5h; Large scale; Stage #2: With hydrogenchloride In water Temperature; Large scale;	92%

...Expand

: 89-64-5
p-chloro-o-nitrophenol

: 100-52-7
benzaldehyde

: 1019-90-5
5-chloro-2-phenyl-1,3-benzoxazole

Conditions

Conditions	Yield
With 1,4-diaza-bicyclo[2.2.2]octane; sulfur at 130℃; for 2h;	92%

: 1440-61-5
N-chloroacetylmorpholine

: 89-64-5
p-chloro-o-nitrophenol

: 708995-00-0
2-(4-Chloro-2-nitro-phenoxy)-1-morpholin-4-yl-ethanone

Conditions

Conditions	Yield
With potassium carbonate In DMF (N,N-dimethyl-formamide) at 70℃;	91%

: 89-64-5
p-chloro-o-nitrophenol

: 122-01-0
4-chloro-benzoyl chloride

: 1290636-91-7
C13H7Cl2NO4

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 20℃; for 1h;	91%

: 149299-82-1
tert-butyl 2-(2-(2-hydroxyethoxy)ethoxy)acetate

: 89-64-5
p-chloro-o-nitrophenol

: 1144518-54-6
{2-[2-(4-chloro-2-nitrophenoxy)ethoxy]ethoxy}acetic acid tert-butyl ester

Conditions

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 0 - 20℃; Mitsunobu reaction;	90%

: 939-97-9
4-tert-Butylbenzaldehyde

: 89-64-5
p-chloro-o-nitrophenol

: 5998-48-1
5-chloro-2-benzoxazole

Conditions

Conditions	Yield
With 1,4-diaza-bicyclo[2.2.2]octane; sulfur at 130℃; for 2h;	90%

: 89-64-5
p-chloro-o-nitrophenol

: 6226-25-1
2,2,2-trifluoroethyl trifluoromethanesulphonate

: 99366-81-1
4-chloro-2-nitro-1-(2,2,2-trifluoroethoxy)benzene

Conditions

Conditions	Yield
With potassium carbonate In acetone at 60℃; for 3h; Inert atmosphere;	90%
With potassium carbonate In acetone Inert atmosphere;	90%

4-Chloro-2-nitrophenol Specification

The IUPAC name of Phenol,4-chloro-2-nitro- is 4-chloro-2-nitrophenol. With the CAS registry number 89-64-5, it is also named as 2-Nitro-4-chlorophenol. The product's categories are Intermediates of Dyes and Pigments; Aromatic Phenols; Phenoles and Thiophenoles; Organic Building Blocks; Oxygen Compounds; Phenols. Besides, it is yellow powder, which is insoluble in water. In addition, its molecular formula is C₆H₄ClNO₃ and molecular weight is 173.56.

The other characteristics of this product can be summarized as: (1)EINECS: 201-927-5; (2)ACD/LogP: 2.75; (3)# of Rule of 5 Violations: 0; (4)ACD/LogD (pH 5.5): 2.69; (5)ACD/LogD (pH 7.4): 1.64; (6)ACD/BCF (pH 5.5): 62.66; (7)ACD/BCF (pH 7.4): 5.62; (8)ACD/KOC (pH 5.5): 646.62; (9)ACD/KOC (pH 7.4): 57.97; (10)#H bond acceptors: 4; (11)#H bond donors: 1; (12)#Freely Rotating Bonds: 2; (13)Index of Refraction: 1.626; (14)Molar Refractivity: 39.57 cm³; (15)Molar Volume: 111.6 cm³; (16)Surface Tension: 62.2 dyne/cm; (17)Density: 1.554 g/cm³; (18)Flash Point: 100.4 °C; (19)Melting point: 85-87 °C; (20)Enthalpy of Vaporization: 49.89 kJ/mol; (21)Boiling Point: 242.5 °C at 760 mmHg; (22)Vapour Pressure: 0.0218 mmHg at 25 °C.

Preparation of Phenol,4-chloro-2-nitro-: this chemical can be prepared by the hydrolysis and acidification of 2,5-Dichloronitrobenzene. It also can be produced by 4-Chloro-phenol.

This reaction needs Fe(NO₃)^.1.5N₂O₄ and Acetone at ambient temperature. The yield is 99 %.

Uses of Phenol,4-chloro-2-nitro-: this chemical can be used as intermediate in organic synthesis and intermediate of dye. Furthermore, it can be used to produce 2-Amino-4-chloro-phenol.

This reaction needs Zinc, Ammonium chloride, H₂O and Ethanol for 25 min. The yield is 48 %.

When you are using this chemical, please be cautious about it as the following: it is irritating to eyes, respiratory system and skin. It is also harmful by inhalation, in contact with skin and if swallowed. In case of contact with eyes, please rinse immediately with plenty of water and seek medical advice. And you should wear suitable protective clothing, gloves and eye/face protection.

People can use the following data to convert to the molecule structure.
(1)SMILES: Clc1cc([N+]([O-])=O)c(O)cc1
(2)InChI: InChI=1/C6H4ClNO3/c7-4-1-2-6(9)5(3-4)8(10)11/h1-3,9H
(3)InChIKey: NWSIFTLPLKCTSX-UHFFFAOYAR
(4)Std. InChI: InChI=1S/C6H4ClNO3/c7-4-1-2-6(9)5(3-4)8(10)11/h1-3,9H
(5)Std. InChIKey: NWSIFTLPLKCTSX-UHFFFAOYSA-N

Product Name

4-CHLORO-2-NITROPHENOL

Synthetic route

4-Chloro-2-nitrophenol Specification

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