Conditions | Yield |
---|---|
Stage #1: 2,4-Dinitroanilin With hydrogenchloride In water at 50 - 70℃; Stage #2: With sodium perchlorate In water at 70℃; for 2h; | 98% |
Stage #1: 2,4-Dinitroanilin With hydrogenchloride In water at 35℃; for 2h; Stage #2: With chlorine In water at 45℃; Stage #3: With dihydrogen peroxide In water at 60 - 65℃; for 6h; Temperature; | 98.4% |
With hydrogenchloride; dmap; dihydrogen peroxide In water at 20 - 30℃; for 3h; Reagent/catalyst; | 97.2% |
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid at 0 - 40℃; for 1h; | 56% |
Multi-step reaction with 3 steps 1: diethyl ether 2: nitric acid / -15 °C / folgendes bei Raumtemperatur 3: water View Scheme |
5-chloro-4-methoxy-1,3-dinitrobenzene
2-chloro-4,6-dinitroaniline
Conditions | Yield |
---|---|
With methanol; ammonia |
Conditions | Yield |
---|---|
With ethanol; ammonia | |
Multi-step reaction with 2 steps 1: aq. NaN3 2: NH3, NaOAc / ethanol View Scheme |
1-chloro-2,3,5-trinitro-benzene
2-chloro-4,6-dinitroaniline
Conditions | Yield |
---|---|
With ethanol; ammonia |
N-ethyl-N'-(2-chloro-4,6-dinitro-phenyl)-N-nitro-urea
2-chloro-4,6-dinitroaniline
Conditions | Yield |
---|---|
With water |
Conditions | Yield |
---|---|
With sulfuric acid; sulfur trioxide; nitric acid |
2-chloro-4,6-dinitrophenyl azide
2-chloro-4,6-dinitroaniline
Conditions | Yield |
---|---|
With ammonia; sodium acetate In ethanol |
hydrogenchloride
chlorine
acetic acid
2,4-Dinitroanilin
2-chloro-4,6-dinitroaniline
Conditions | Yield |
---|---|
at 15 - 20℃; |
Conditions | Yield |
---|---|
at 105℃; im Rohr; |
5-chloro-4-methoxy-1,3-dinitrobenzene
2-chloro-4,6-dinitroaniline
Conditions | Yield |
---|---|
at 100℃; |
ethanol
N-ethyl-N'-(2-chloro-4,6-dinitro-phenyl)-N-nitro-urea
ammonia
2-chloro-4,6-dinitroaniline
Conditions | Yield |
---|---|
at 100℃; |
N-ethyl-N'-(2-chloro-4,6-dinitro-phenyl)-N-nitro-urea
water
A
ethylnitramine
B
2-chloro-4,6-dinitroaniline
C
methylammonium carbonate
N-ethyl-N'-(2-chloro-phenyl)-urea
2-chloro-4,6-dinitroaniline
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: nitric acid / -15 °C / folgendes bei Raumtemperatur 2: water View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: oleum; fuming nitric acid / 160 - 170 °C 2: alcohol; ammonia View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: alcohol; ammonia View Scheme | |
Multi-step reaction with 2 steps 1: diethylaniline 2: alcohol; ammonia View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: nitrosylsulfuric acid / Diazotization.man traegt die Diazoniumsalz-Loesung in Kupfer(I)-chlorid-Loesung ein 2: oleum; fuming nitric acid / 160 - 170 °C 3: alcohol; ammonia View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: concentrated sulfuric acid / 110 °C 2: hydrochloric acid; potassium chlorate View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: HNO3+H2SO4 2: alcohol; ammonia View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: nitric acid / 0 °C 2: concentrated sulfuric acid / 110 °C 3: hydrochloric acid; potassium chlorate View Scheme |
Conditions | Yield |
---|---|
Stage #1: 2-chloro-4,6-dinitroaniline With sodium hydroxide In water for 0.5h; Stage #2: pyridine-2-carbonyl chloride In water at 5 - 20℃; for 3h; | 95% |
2-chloro-4,6-dinitroaniline
benzoyl chloride
N-(6-chloro-2,4-dinitrophenyl)benzamide
Conditions | Yield |
---|---|
Stage #1: 2-chloro-4,6-dinitroaniline With sodium hydroxide In water for 0.5h; Stage #2: benzoyl chloride In water at 5 - 20℃; for 3h; | 91% |
With pyridine |
2-benzofuroyl chloride
2-chloro-4,6-dinitroaniline
Conditions | Yield |
---|---|
Stage #1: 2-chloro-4,6-dinitroaniline With sodium hydroxide In water for 0.5h; Stage #2: 2-benzofuroyl chloride In water at 5 - 20℃; for 3h; | 90% |
5-nitrofuran-2-carboxylic chloride
2-chloro-4,6-dinitroaniline
Conditions | Yield |
---|---|
Stage #1: 2-chloro-4,6-dinitroaniline With sodium hydroxide In water for 0.5h; Stage #2: 5-nitrofuran-2-carboxylic chloride In water at 5 - 20℃; for 3h; | 90% |
2-chloro-4,6-dinitroaniline
isooxazole-5-carbonyl chloride
Conditions | Yield |
---|---|
Stage #1: 2-chloro-4,6-dinitroaniline With sodium hydroxide In water for 0.5h; Stage #2: isooxazole-5-carbonyl chloride In water at 5 - 20℃; for 3h; | 87% |
Conditions | Yield |
---|---|
With copper(II) acetate monohydrate In neat (no solvent) at 100℃; under 7600.51 Torr; for 20h; Autoclave; Inert atmosphere; Green chemistry; | 75% |
2-chloro-4,6-dinitroaniline
4-nitro-benzoyl chloride
2',4',4-trinitro-6'-chlorobenzanilide
Conditions | Yield |
---|---|
In nitrobenzene at 190 - 200℃; for 4h; | 74% |
Conditions | Yield |
---|---|
Stage #1: 2-chloro-4,6-dinitroaniline; acetic acid With tin(II) chloride dihdyrate for 4h; Reflux; Stage #2: With hydrogenchloride In water for 1h; Reflux; | 69% |
6-(9-carbazolyl)-3-oxahexane-1,5-diol
2-chloro-4,6-dinitroaniline
Conditions | Yield |
---|---|
Stage #1: 2-chloro-4,6-dinitroaniline With sulfuric acid; sodium nitrite In water; acetic acid at 15℃; for 1h; Stage #2: 6-(9-carbazolyl)-3-oxahexane-1,5-diol In 2-methyl-propan-1-ol; water for 1h; | 36% |
formic acid
2-chloro-4,6-dinitroaniline
A
5-amino-4,7-dichlorobenzimidazole
B
7(4)-chloro-5(6)-formylaminobenzimidazole
Conditions | Yield |
---|---|
With hydrogenchloride; tin for 6h; Heating; | A 23.5% B 20% |
2-chloro-4,6-dinitroaniline
1-chloro-2-iodo-3,5-dinitrobenzene
Conditions | Yield |
---|---|
With sulfuric acid; acetic acid Diazotization.Eintragen des Reaktionsgemisches in gesaettigte wss. KI-Loesung; | |
Stage #1: 2-chloro-4,6-dinitroaniline With sulfuric acid; acetic acid; sodium nitrite at 70℃; Stage #2: With potassium iodide In water at 50℃; for 0.25h; |
2-chloro-4,6-dinitroaniline
acetic anhydride
acetic acid-(2-chloro-4,6-dinitro-anilide)
Conditions | Yield |
---|---|
With sulfuric acid; acetic acid | |
With sulfuric acid |
carbon disulfide
2-chloro-4,6-dinitroaniline
sodium monochloroacetic acid
3-(2-chloro-4,6-dinitro-phenyl)-2-thioxo-thiazolidin-4-one
Conditions | Yield |
---|---|
(i) aq. NH3, (ii) /BRN= 3597157/; Multistep reaction; |
4-chloro-3,5-dinitrobenzotrifluoride
2-chloro-4,6-dinitroaniline
6'-chloro-4-trifluoromethyl-2,2',4',6-tetranitrodiphenylamine
Conditions | Yield |
---|---|
In N-methyl-acetamide | |
With sodium hydride |
5-aminonaphthalene-2-sulfonic acid
2-chloro-4,6-dinitroaniline
C47H49ClN6O10S
Conditions | Yield |
---|---|
Multistep reaction; |
1-chloro-2,4-dinitro-6-trifluoromethylbenzene
2-chloro-4,6-dinitroaniline
(2-Chloro-4,6-dinitro-phenyl)-(2,4-dinitro-6-trifluoromethyl-phenyl)-amine
2-chloro-4,6-dinitroaniline
C49H52ClN7O11S
Conditions | Yield |
---|---|
Multistep reaction; |
2-chloro-4,6-dinitroaniline
6-chloro-2,4-diaminobenzimidazole
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In methanol; formic acid at 20℃; under 2280 Torr; for 23h; |
Chemical Name: 2-Chloro-4,6-dinitroaniline
IUPAC NAME: 2-chloro-4,6-dinitroaniline
CAS No.: 3531-19-9
EINECS: 222-564-9
RTECS: BX9250000
RTECS Class: Mutagen
Molecular Formula: C6H4ClN3O4
Molecular Weight: 217.57 g/mol
Density: 1.708 g/cm3
Melting Point: 157-159 °C(lit.)
Flash Point: 181.4 °C
Boiling Point: 376.3 °C at 760 mmHg
The yellow powder insoltble in water,it is stable at room temperature in closed containers under normal storage and handling conditions.Following is the structure of 2-CHLORO-4,6-DINITROANILINE(3531-19-9):
The chemical synonymous of 2-CHLORO-4,6-DINITROANILINE(3531-19-9) are 2-chloro-4,6-dinitro-benzenamin;2-chloro-4,6-dinitro-Benzenamine;6-chloro-2,4-dinitro-anilin;LABOTEST-BB LT00159757;2-CHLORO-4,6-DINITROANILINE;2,6-DINITRO-4-CHLOROANILINE;TIMTEC-BB SBB003373;TIMTEC-BB SBB003374
Product Categories about 2-CHLORO-4,6-DINITROANILINE(3531-19-9) are Intermediates of Dyes and Pigments;Amines;C2 to C6;Nitrogen Compounds.
1. | mmo-sat 500 µg/plate | SAIGBL Sangyo Igaku. Japanese Journal of Industrial Health. 29 (1987),34. |
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