ChemicalBook--->CAS DataBase List--->5900-59-4

5900-59-4

5900-59-4 Structure

5900-59-4 Structure
IdentificationBack Directory
[Name]

2-amino-4-chlorobenzamide
[CAS]

5900-59-4
[Synonyms]

4-Chloroanthranilamide
2-aMino-4-chlrobenzaMide
2-amino-4-chlorobenzamide
Benzamide, 2-amino-4-chloro-
2-amino-4-chlorophenylformamide
2-amino-4-chlorobenzamide(SALTDATA: FREE)
[EINECS(EC#)]

200-002-4
[Molecular Formula]

C7H7ClN2O
[MDL Number]

MFCD09042792
[MOL File]

5900-59-4.mol
[Molecular Weight]

170.6
Chemical PropertiesBack Directory
[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
Questions And AnswerBack Directory
[Uses]

2-Amino-4-chlorobenzamide is a useful research chemical.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H302-H317
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P-P261-P272-P280-P302+P352-P333+P313-P321-P363-P501
[Risk Statements ]

43
[Safety Statements ]

36/37
[HS Code ]

2924297099
Spectrum DetailBack Directory
[Spectrum Detail]

2-amino-4-chlorobenzamide(5900-59-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Amino-4-chlorobenzoic acid

89-77-0

2-amino-4-chlorobenzamide

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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