2-amino-4-chlorobenzamide

2-amino-4-chlorobenzamide Suppliers list
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Products Intro: Product Name:2-Amino-4-chlorobenzamide
CAS:5900-59-4
Purity:99%(Min,HPLC) Package:1G;1KG;100KG
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Products Intro: Product Name:2-Amino-4-chlorobenzamide
CAS:5900-59-4
Purity:0.98 Package:25KG;5KG;1KG
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CAS:5900-59-4
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Products Intro: Product Name:2-Amino-4-Chlorobenzamide
CAS:5900-59-4
Purity:0.98 Package:1KG;10KG;50KG

2-amino-4-chlorobenzamide manufacturers

2-amino-4-chlorobenzamide Basic information
Uses
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
Product Categories:
Mol File:5900-59-4.mol
2-amino-4-chlorobenzamide Structure
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
pka15.48±0.50(Predicted)
form solid
AppearanceOff-white to light yellow Solid
InChI1S/C7H7ClN2O/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3H,9H2,(H2,10,11)
InChIKeyQNEJYHVIYJFNHC-UHFFFAOYSA-N
SMILESO=C(N)C(C(N)=C1)=CC=C1Cl
Safety Information
Risk Statements 43
Safety Statements 36/37
WGK Germany WGK 3
HS Code 2924297099
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
Skin Sens. 1
MSDS Information
2-amino-4-chlorobenzamide Usage And Synthesis
Uses2-Amino-4-chlorobenzamide is a useful research chemical.
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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