Basic information Safety Supplier Related

2-AMINO-4-CHLOROBENZOIC ACID

Basic information Safety Supplier Related

2-AMINO-4-CHLOROBENZOIC ACID Basic information

Product Name:
2-AMINO-4-CHLOROBENZOIC ACID
Synonyms:
  • LABOTEST-BB LT00454298
  • METHYL 4-CHLOROANTHRANILATE
  • METHYL 2-AMINO-4-CHLOROBENZOATE
  • 2,4-ACBA
  • 2-CARBOXY-5-CHLOROANILINE
  • 2-AMINO-4-CHLOROBENZOIC ACID METHYL ESTER
  • 3-AMINO-4-CARBOXY-1-CHLOROBENZENE
  • 4-CHLOROANTHRANILIC ACID METHYL ESTER
CAS:
5900-58-3
MF:
C8H8ClNO2
MW:
185.61
EINECS:
227-593-0
Product Categories:
  • FINE Chemical & INTERMEDIATES
  • Aromatic Esters
  • Phenylacetic acid
Mol File:
5900-58-3.mol
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2-AMINO-4-CHLOROBENZOIC ACID Chemical Properties

Melting point:
66-71 °C
Boiling point:
284.0±20.0 °C(Predicted)
Density 
1.311±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
solid
pka
1.33±0.10(Predicted)
color 
Light brown
BRN 
1072895
InChI
InChI=1S/C8H8ClNO2/c1-12-8(11)6-3-2-5(9)4-7(6)10/h2-4H,10H2,1H3
InChIKey
YPSSCICDVDOEAI-UHFFFAOYSA-N
SMILES
C(OC)(=O)C1=CC=C(Cl)C=C1N
CAS DataBase Reference
5900-58-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
RTECS 
DG1570000
HS Code 
29224999

MSDS

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2-AMINO-4-CHLOROBENZOIC ACID Usage And Synthesis

Synthesis Reference(s)

Journal of the American Chemical Society, 68, p. 1285, 1946 DOI: 10.1021/ja01211a049

Synthesis

67-56-1

89-77-0

5900-58-3

To a single-necked flask was added 10 g of 2-amino-4-chlorobenzoic acid and 150 ml of methanol, and the mixture was cooled to 0-5 °C. 10.4 g of thionyl chloride was slowly added dropwise with stirring. After the dropwise addition, the reaction mixture was heated to reflux for 24 hours. After completion of the reaction, it was cooled to room temperature and methanol was removed by distillation under reduced pressure. To the residue, 100 ml of ethyl acetate and 100 ml of 5% sodium carbonate solution were added, stirred thoroughly and left to stratify. The aqueous layer was separated and the organic layer was washed with 100 ml of water. The organic phase was dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give 8.9 g of methyl 2-amino-4-chlorobenzoate in 82% yield.

References

[1] Journal of Medicinal Chemistry, 1996, vol. 39, # 17, p. 3248 - 3255
[2] Patent: CN106243046, 2016, A. Location in patent: Paragraph 0047; 0052; 0053; 0073; 0074
[3] Patent: CN107778229, 2018, A. Location in patent: Paragraph 0021
[4] Patent: WO2010/65134, 2010, A1. Location in patent: Page/Page column 60
[5] Journal of the Chemical Society, 1947, p. 808,811

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