Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Chemical Reagents >  Organic reagents >  Esters >  Methyl ester compound >  METHYL 4-AMINO-3-CHLOROBENZOATE

METHYL 4-AMINO-3-CHLOROBENZOATE

Basic information Safety Supplier Related

METHYL 4-AMINO-3-CHLOROBENZOATE Basic information

Product Name:
METHYL 4-AMINO-3-CHLOROBENZOATE
Synonyms:
  • TIMTEC-BB SBB003712
  • METHYL 4-AMINO-3-CHLOROBENZOATE
  • Methyl4-amino-3-chlorobenzoate98%
  • AKOS BB-3098
  • 4-AMINO-3-CHLORO-BENZOIC ACID METHYL ESTER
  • 2-Chloro-4-(methoxycarbonyl)aniline
  • Methyl 4-aMino-3-chlorobenzoate, 97% 5GR
  • Benzoic acid, 4-aMino-3-chloro-, Methyl ester
CAS:
84228-44-4
MF:
C8H8ClNO2
MW:
185.61
Product Categories:
  • Aromatic Esters
  • C8 to C9
  • Carbonyl Compounds
  • Esters
Mol File:
84228-44-4.mol
More
Less

METHYL 4-AMINO-3-CHLOROBENZOATE Chemical Properties

Melting point:
107-111 °C
Boiling point:
321.6±22.0 °C(Predicted)
Density 
1.2797 (rough estimate)
refractive index 
1.5560 (estimate)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
0.52±0.10(Predicted)
form 
Crystalline Powder
color 
Beige-brown
CAS DataBase Reference
84228-44-4(CAS DataBase Reference)
More
Less

Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
22
Safety Statements 
36/37
WGK Germany 
2
Hazard Note 
Irritant
HS Code 
29224985

MSDS

More
Less

METHYL 4-AMINO-3-CHLOROBENZOATE Usage And Synthesis

Chemical Properties

beige-brown crystals or crystalline powder

Synthesis

67-56-1

2486-71-7

84228-44-4

Concentrated sulfuric acid (2.00 mL) was added slowly and dropwise to a stirred solution of 3-chloro-4-aminobenzoic acid (2.00 g, 11.7 mmol) in methanol (20.0 mL) at 0 °C. The reaction mixture was warmed to 80 °C and kept stirring for 6 hours. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently concentrated under reduced pressure. The concentrated residue was diluted with saturated aqueous sodium bicarbonate and extracted with ethyl acetate (2 x 50 mL). The organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give methyl 4-amino-3-chlorobenzoate (2.10 g, 97% yield). The product was confirmed by NMR hydrogen spectroscopy (400 MHz, DMSO-d6): δ 7.70 (d, J = 1.6Hz, 1H), 7.58 (dd, J = 8.4, 2.0Hz, 1H), 6.77 (d, J = 8.8Hz, 1H), 6.24 (s, 2H), 3.73 (s, 3H).

References

[1] Patent: WO2011/128251, 2011, A1. Location in patent: Page/Page column 203
[2] Patent: US2011/257151, 2011, A1. Location in patent: Page/Page column 75
[3] Patent: WO2018/157190, 2018, A1. Location in patent: Paragraph 0337
[4] Journal of Cellular Biochemistry, 2017, vol. 118, # 8, p. 2420 - 2429
[5] Journal of Medicinal Chemistry, 2018, vol. 61, # 3, p. 666 - 680

METHYL 4-AMINO-3-CHLOROBENZOATESupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
INTATRADE GmbH
Tel
+49 3493/605464
Email
sales@intatrade.de
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Email
Sales-CN@TCIchemicals.com