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Benzamide, 2,3-diamino-

CAS No.
711007-44-2
Chemical Name:
Benzamide, 2,3-diamino-
Synonyms
Benzamide, 2,3-diamino-
CBNumber:
CB11482172
Molecular Formula:
C7H9N3O
Molecular Weight:
151.17
MDL Number:
MFCD09029906
MOL File:
711007-44-2.mol
Last updated:2025-07-24 18:13:47
Product description Number Pack Size Price
2,3-Diaminobenzamide D422630 100mg $75
2,3-Diaminobenzamide FD144358 250mg $82.5
2,3-diaminobenzamide 98.13% CS-M0574 5g $118
2,3-Diaminobenzamide FD144358 500mg $145
2,3-Diaminobenzamide FD144358 1g $253
More product size

Benzamide, 2,3-diamino- Properties

Boiling point 315.0±27.0 °C(Predicted)
Density 1.341±0.06 g/cm3 (20 ºC 760 Torr)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka 16.03±0.50(Predicted)
Appearance Light brown to brown Solid

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS06,GHS08,GHS09
Signal word  Danger
Hazard statements  H301-H312+H332-H317-H319-H341-H351-H371-H411
Precautionary statements  P273-P280-P301+P310
Risk Statements  36/37/38
Safety Statements  26-36
RIDADR  2811
HazardClass  6.1
PackingGroup 
HS Code  29242990

Benzamide, 2,3-diamino- price More Price(25)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC D422630 2,3-Diaminobenzamide 711007-44-2 100mg $75 2021-12-16 Buy
Biosynth Carbosynth FD144358 2,3-Diaminobenzamide 711007-44-2 250mg $82.5 2021-12-16 Buy
ChemScene CS-M0574 2,3-diaminobenzamide 98.13% 711007-44-2 5g $118 2021-12-16 Buy
Biosynth Carbosynth FD144358 2,3-Diaminobenzamide 711007-44-2 500mg $145 2021-12-16 Buy
Biosynth Carbosynth FD144358 2,3-Diaminobenzamide 711007-44-2 1g $253 2021-12-16 Buy
Product number Packaging Price Buy
D422630 100mg $75 Buy
FD144358 250mg $82.5 Buy
CS-M0574 5g $118 Buy
FD144358 500mg $145 Buy
FD144358 1g $253 Buy

Benzamide, 2,3-diamino- Chemical Properties,Uses,Production

Synthesis

2-Amino-3-nitrobenzamide

313279-12-8

Benzamide, 2,3-diamino-

711007-44-2

The general procedure for the synthesis of 2,3-diaminobenzamide from 2-amino-3-nitrobenzamide is as follows: 1. 2-Amino-3-nitrobenzoic acid (3.00 g, 16.47 mmol) was dissolved in dimethoxyethane (15 ml), thionyl chloride (2.61 g, 21.91 mmol) was added, and the mixture was stirred at 50 °C for 12 hours. After completion of the reaction, the solvent was removed by concentration under reduced pressure and concentrated again by adding toluene. Subsequently, saturated aqueous ammonia solution (40 ml) was added to a round-bottom flask and cooled to 10 °C, and unpurified chloroyl chloride (3.30 g, 16.45 mmol) was slowly added dropwise, keeping the reaction temperature below 40 °C. After dropwise addition, the mixture was stirred at 50 °C for 1 h. The mixture was diluted with water and stirred at room temperature. The orange precipitate was collected by filtration, washed with water and dried to give 2-amino-3-nitrobenzamide (2.60 g, 87% yield). 2. A methanolic solution (80 ml) of 2-amino-3-nitrobenzamide (2.60 g, 14.35 mmol) with a palladium/carbon catalyst (aqueous wet, 10% Pd, 0.05 eq, 0.072 mmol) was placed in a metal vessel. Hydrogen was passed in a laboratory reactor and stirred for 5 h at room temperature and 2 bar pressure. After the reaction was complete, the catalyst was removed by diatomaceous earth filtration and the filtrate was washed with methanol. The filtrate was concentrated under reduced pressure and the residue was extracted with water and ethyl acetate. The organic phases were combined, dried over magnesium sulfate, filtered and concentrated to afford 2,3-diaminobenzamide (2.15 g, 98% yield) of >95% purity without further purification. 3. 2,3-Diaminobenzamide (200 mg, 1.32 mmol) was dissolved in chlorodifluoroacetic acid (3 ml) and refluxed for 3 hours with vigorous stirring. After cooling to room temperature, NaHCO3 solution was added and 2-[chloro(difluoromethyl)-1H-benzimidazole-4-carboxamide (190 mg, 58% yield) was precipitated as a colorless solid, pumped, washed with water and dried. Product characterization data: 1H NMR (400 MHz, d6-DMSO δ, ppm) 14.40 (br.s, 1H, NH), 8.72 (br.s, 1H, NH), 8.02 (m, 1H, NH), 7.92 (m, 1H), 7.74 (m, 1H), 7.55 (m, 1H); 13C NMR (150MHz d6-DMSO δ, ppm) 165.5, 147.9, 139.1, 134.2, 124.9, 124.5, 123.9, 118.4-122.2 (t, CF2Cl), 116.6.

References

[1] Bioorganic and Medicinal Chemistry Letters, 2004, vol. 14, # 10, p. 2433 - 2437
[2] Patent: US2011/218103, 2011, A1. Location in patent: Page/Page column 11
[3] Patent: EP2561759, 2013, A1. Location in patent: Paragraph 0051
[4] Patent: WO2004/96793, 2004, A1. Location in patent: Page 14
[5] Journal of Medicinal Chemistry, 2000, vol. 43, # 22, p. 4084 - 4097

Benzamide, 2,3-diamino- Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 96)Suppliers
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Aromsyn Co., Ltd.
+86-0571-85585865 +8613336024896 CB@aromsyn.com China 19183 58
Hebei Chuanghai Biotechnology Co., Ltd
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View Lastest Price from Benzamide, 2,3-diamino- manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2,3-Diaminobenzamide pictures 2024-11-26 2,3-Diaminobenzamide
711007-44-2
US $0.00-0.00 / kg 1kg 98% 1 ton Nanjing Fred Technology Co., Ltd
Benzamide, 2,3-diamino- pictures 2019-07-06 Benzamide, 2,3-diamino-
711007-44-2
US $1.00 / KG 1KG 99% 1ton Career Henan Chemical Co

Benzamide, 2,3-diamino- Spectrum

Benzamide, 2,3-diamino- 711007-44-2 711077-44-2