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5-broMo-1H-indole-7-carboxaMide

CAS No.
860624-91-5
Chemical Name:
5-broMo-1H-indole-7-carboxaMide
Synonyms
5-broMo-1H-indole-7-carboxaMid;5-broMo-1H-indole-7-carboxaMide;1H-Indole-7-carboxamide, 5-bromo-
CBNumber:
CB62563127
Molecular Formula:
C9H7BrN2O
Molecular Weight:
239.07
MDL Number:
MFCD27930237
MOL File:
860624-91-5.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:51
Product description Number Pack Size Price
5-bromo-1H-indole-7-carboxamide 95+% CD11042713 1g $518
5-bromo-1H-indole-7-carboxamide 95% A420214 250mg $181
5-bromo-1H-indole-7-carboxamide 860624915 1g $413.56
5-bromo-1H-indole-7-carboxamide 95% CM146753 1g $489

5-broMo-1H-indole-7-carboxaMide Properties

storage temp. Sealed in dry,Room Temperature

5-broMo-1H-indole-7-carboxaMide price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Crysdot CD11042713 5-bromo-1H-indole-7-carboxamide 95+% 860624-91-5 1g $518 2026-05-26 Buy
Ambeed A420214 5-bromo-1H-indole-7-carboxamide 95% 860624-91-5 250mg $181 2021-12-16 Buy
Alichem 860624915 5-bromo-1H-indole-7-carboxamide 860624-91-5 1g $413.56 2021-12-16 Buy
Chemenu CM146753 5-bromo-1H-indole-7-carboxamide 95% 860624-91-5 1g $489 2021-12-16 Buy
Product number Packaging Price Buy
CD11042713 1g $518 Buy
A420214 250mg $181 Buy
860624915 1g $413.56 Buy
CM146753 1g $489 Buy

5-broMo-1H-indole-7-carboxaMide Chemical Properties,Uses,Production

Synthesis

5-BROMO INDOLE-7-CARBOXYLIC ACID

860624-90-4

5-broMo-1H-indole-7-carboxaMide

860624-91-5

General procedure for the synthesis of 5-bromo-1H-indole-7-carboxylic acid from 5-bromo-1H-indole-7-carboxylic acid: 5-bromo-1H-indole-7-carboxylic acid (10.0 g, 42 mmol) was dissolved in dichloromethane (100 mL) at room temperature, and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC, 9.66 g, 50.4 mmol) was added sequentially. 50.4 mmol), 1-hydroxybenzotriazole (HOBt, 6.81 g, 50.4 mmol) and a methanol solution of ammonia (2.0 M, 84 mL, 168 mmol). The reaction mixture was stirred at room temperature for 16 hours. After completion of the reaction, the solvent was removed by evaporation and the residue was extracted by partitioning with ethyl acetate (100 mL) and water (100 mL). The aqueous layer was then extracted twice with ethyl acetate (100 mL x 2), and all organic phases were combined, dried with anhydrous magnesium sulfate, and concentrated to give the crude product 5-bromo-1H-indole-7-carboxamide (10 g, 98% yield). The crude product did not require further purification and could be used directly in the subsequent reaction.LC/MS analysis: m/z 240.0 ([M+H]+), retention time 1.95 min.

References

[1] Patent: US2009/143372, 2009, A1
[2] Patent: WO2005/67923, 2005, A1. Location in patent: Page/Page column 51
[3] Patent: WO2006/34317, 2006, A2. Location in patent: Page/Page column 78
[4] Patent: WO2007/62318, 2007, A2. Location in patent: Page/Page column 40
[5] Patent: WO2005/67923, 2005, A1. Location in patent: Page/Page column 39-40

5-broMo-1H-indole-7-carboxaMide Preparation Products And Raw materials

5-broMo-1H-indole-7-carboxaMide Suppliers

Global( 16)Suppliers
Supplier Tel Email Country ProdList Advantage
Amadis Chemical Company Limited
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Wuhan TCASChem Technology Co., Ltd. 027-86697669 13986148687 sales@tcaschem.com China 4000 55
ShangHai Angti Biotechnology Co., Ltd. 13764913901 info@angtibio.com China 4977 55
Aikon International Limited 025-58859352 13913916777 dt3@aikonchem.com China 15490 58
Nanjing SynTitan Pharmaceutical Co., Ltd. 025-57027686 17372956142 li_lan@syntitan.com China 9999 58
Changzhou Kechem Bio-Scientific Co., LTD. 0519-68985668 13685222090 sales@kechem.cn China 26012 58
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Allbio pharm Co., Ltd 1483287082 19962651230 sales@allbiopharm.com China 1420 58
Wuhan Wanjian Biotechnology Co., Ltd 13277087647 17771779698@qq.com China 9986 58
5-broMo-1H-indole-7-carboxaMide 1H-Indole-7-carboxamide, 5-bromo- 5-broMo-1H-indole-7-carboxaMid 860624-91-5