Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyridine compound >  Pyridine derivatives >  3-Chloro-2-nitroaniline

3-Chloro-2-nitroaniline

Basic information Safety Supplier Related

3-Chloro-2-nitroaniline Basic information

Product Name:
3-Chloro-2-nitroaniline
Synonyms:
  • TIMTEC-BB SBB008617
  • 3-CHLORO-2-NITRO-PHENYLAMINE
  • 3-CHLORO-2-NITROANILINE
  • 2-Amino-6-chloronitrobenzene
  • 3-Chloro-2-nitroaniline, 95+%
  • Benzenamine, 3-chloro-2-nitro-
  • 3-CHLORO-2-NITROANILINE ---YELLOW POWDER, 98%---
  • 2-Nitro-3-chloroaniline
CAS:
59483-54-4
MF:
C6H5ClN2O2
MW:
172.57
EINECS:
261-782-9
Product Categories:
  • Amines
  • blocks
  • NitroCompounds
  • Pyridines
  • Anilines, Aromatic Amines and Nitro Compounds
Mol File:
59483-54-4.mol
More
Less

3-Chloro-2-nitroaniline Chemical Properties

Melting point:
107-108°C
Boiling point:
327.1±22.0 °C(Predicted)
Density 
1.494±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
-1.29±0.10(Predicted)
Appearance
Orange to red Solid
InChI
InChI=1S/C6H5ClN2O2/c7-4-2-1-3-5(8)6(4)9(10)11/h1-3H,8H2
InChIKey
YADOEPHJIBKBCN-UHFFFAOYSA-N
SMILES
C1(N)=CC=CC(Cl)=C1[N+]([O-])=O
CAS DataBase Reference
59483-54-4(CAS DataBase Reference)
More
Less

Safety Information

Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-36/37/39
HS Code 
2921420090
More
Less

3-Chloro-2-nitroaniline Usage And Synthesis

Chemical Properties

red powder

Synthesis

4771-47-5

59483-54-4

General procedure for the synthesis of 3-chloro-2-nitroaniline from 3-chloro-2-nitrobenzoic acid: 3-chloro-2-nitrobenzoic acid (20 g, 99 mmol) and triethylamine (Et3N, 20.74 mL, 149 mmol) were dissolved in N,N-dimethylformamide (DMF, 100 mL), followed by the addition of diphenylphosphonium chloride (32.8 g, 119 mmol). The reaction mixture was stirred at room temperature for 3 hours. Next, water (200 mL) was added to the reaction mixture and heated at 100 °C for 1 hour. After the reaction was completed, the solution was cooled to room temperature. The device was short range distillation head and DMF was removed by high vacuum distillation. the remaining solid was dissolved in ethyl acetate (EtOAc) and washed with saturated sodium bicarbonate (NaHCO3) solution. The organic phase was filtered through diatomaceous earth, the filtrate was washed sequentially with water (3 times) and brine, dried over anhydrous sodium sulfate (Na2SO4), filtered, and concentrated under reduced pressure to afford the target product 3-chloro-2-nitroaniline 10 g in 53.4% yield. m/z 173.1 (M + H)+ with retention time of 1.67 min by LC-MS.

References

[1] Patent: WO2015/92713, 2015, A1. Location in patent: Page/Page column 273
[2] Journal of Organic Chemistry, 1977, vol. 42, # 1, p. 166 - 169
[3] Journal of Medicinal Chemistry, 1993, vol. 36, # 11, p. 1630 - 1640
[4] Journal of Medicinal Chemistry, 1992, vol. 35, # 23, p. 4455 - 4463
[5] Patent: US6358946, 2002, B1. Location in patent: Page column 5

3-Chloro-2-nitroanilineSupplier

Shanghai Harvest Chemical Industrial Co., Ltd. Gold
Tel
021-31038972,31038973 17321035817
Email
sales@harvest-chem.com
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
ShangHai DEMO Chemical Co.,Ltd
Tel
400-021-7337 2355568890
Email
sales@demochem.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Shijiazhuang Sdyano Fine Chemical Co., Ltd.
Tel
0311-89250318 031166536426
Email
master@sjzsdyn.com