Basic information Uses Safety Supplier Related

2-amino-4-chlorobenzamide

Basic information Uses Safety Supplier Related

2-amino-4-chlorobenzamide Basic information

Product Name:
2-amino-4-chlorobenzamide
Synonyms:
  • 2-amino-4-chlorobenzamide
  • 2-amino-4-chlorobenzamide(SALTDATA: FREE)
  • 2-aMino-4-chlrobenzaMide
  • 4-Chloroanthranilamide
  • 2-amino-4-chlorophenylformamide
  • Benzamide, 2-amino-4-chloro-
CAS:
5900-59-4
MF:
C7H7ClN2O
MW:
170.6
EINECS:
200-002-4
Mol File:
5900-59-4.mol
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2-amino-4-chlorobenzamide Chemical Properties

Melting point:
181.5 °C
Boiling point:
308.8±27.0 °C(Predicted)
Density 
1.394±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
solid
pka
15.48±0.50(Predicted)
Appearance
Off-white to light yellow Solid
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Safety Information

Risk Statements 
43
Safety Statements 
36/37
HS Code 
2924297099
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2-amino-4-chlorobenzamide Usage And Synthesis

Uses

2-Amino-4-chlorobenzamide is a useful research chemical.

Synthesis

89-77-0

5900-59-4

Method I: Synthesis of 2-amino-4-chlorobenzamide (ii-b) 1. 2-Amino-4-chlorobenzoic acid (3.42 g, 20 mmol) was dissolved in DMF (45 mL) and HOBt (2.70 g, 20 mmol) was added. 2. After stirring for 10 min, EDC-HCl (3.82 g, 20 mmol) was added to the mixture. 3. the reaction mixture was stirred at room temperature for 2 hr. 4. NH4OH (28%, 5 mL) was slowly added at 0 °C with vigorous stirring. 5. After addition, continue stirring at room temperature for 2 hours. 6. The reaction mixture was added slowly dropwise to water (200 mL) and a precipitate was precipitated. 7. The precipitate was collected by filtration and dried under vacuum to give 2.98 g of the target product ii-b as a gray solid in 87.6% yield. 8. 8. The product was characterized by LCMS m/z = 171.0 (M + 1), 173.0 (M + 3) (Method B) (retention time = 1.39 min). 1H NMR (400 MHz, DMSO-d6): δ 7.27 (d, J = 9.6 Hz, 1H), 6.68 (d, J = 2.4 Hz, 1H), 6.60 (dd, J = 8.4, 2.0 Hz, 1H), 5.50-5.82 (m, 4H).

References

[1] European Journal of Medicinal Chemistry, 2018, vol. 157, p. 1361 - 1375
[2] Patent: US2015/307477, 2015, A1. Location in patent: Paragraph 1473
[3] Patent: JP6121658, 2017, B2. Location in patent: Paragraph 1063; 1064; 1065
[4] Patent: WO2010/99379, 2010, A1. Location in patent: Page/Page column 142
[5] Arkivoc, 2012, vol. 2012, # 8, p. 198 - 213

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