ChemicalBook > CAS DataBase List > 4-bromo-1H-indole-7-carboxamide

4-bromo-1H-indole-7-carboxamide

Product Name
4-bromo-1H-indole-7-carboxamide
CAS No.
1211596-82-5
Chemical Name
4-bromo-1H-indole-7-carboxamide
Synonyms
4-bromo-1H-indole-7-carboxamide;1H-Indole-7-carboxaMide, 4-broMo-
CBNumber
CB32514966
Molecular Formula
C9H7BrN2O
Formula Weight
239.07
MOL File
1211596-82-5.mol
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4-bromo-1H-indole-7-carboxamide Property

storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
White to off-white Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H317May cause an allergic skin reaction

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

TRC
Product number
B111595
Product name
4-Bromo-1H-indole-7-carboxamide
Packaging
10mg
Price
$45
Updated
2021/12/16
AK Scientific
Product number
Z2821
Product name
4-Bromo-1H-indole-7-carboxamide
Packaging
50mg
Price
$252
Updated
2021/12/16
AK Scientific
Product number
Z2821
Product name
4-Bromo-1H-indole-7-carboxamide
Packaging
100mg
Price
$353
Updated
2021/12/16
Matrix Scientific
Product number
188191
Product name
4-Bromo-1H-indole-7-carboxamide
Packaging
500mg
Price
$420
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0098632
Product name
4-BROMO-1H-INDOLE-7-CARBOXAMIDE
Purity
95.00%
Packaging
5MG
Price
$496.77
Updated
2021/12/16
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4-bromo-1H-indole-7-carboxamide Chemical Properties,Usage,Production

Synthesis

1211594-25-0

1211596-82-5

4-Bromo-1H-indole-7-carboxylic acid (5.5 g, 22.91 mmol) was used as a starting material and dissolved with EDC (6.59 g, 34.4 mmol) and HOBt (5.26 g, 34.4 mmol) in a solvent mixture of THF (150 mL) and DCM (180 mL). The reaction mixture was stirred at room temperature for 1 h to activate the carboxyl groups. Subsequently, NH3 gas was passed into the reaction system for about 15 minutes and stirring was continued overnight at room temperature to complete the amidation reaction. Upon completion of the reaction, the reaction mixture was diluted by addition of water and extracted with DCM. The organic phases were combined, washed with brine, dried over anhydrous sodium sulfate and concentrated to give the crude product. The crude product was suspended in ether and filtered to give 4-bromo-1H-indole-7-carboxamide (5.3 g, 97% yield) as a white solid. The structure of the product was confirmed by 1H NMR (DMSO-d6): δ 11.40 (br, 1H), 8.08 (br, 1H), 7.29-7.57 (d, J = 7.6 Hz, 1H), 7.43-7.42 (m, 2H), 7.28-7.26 (d, J = 7.6 Hz, 1H), 6.43-6.42 (m, 1H).

References

[1] Patent: WO2014/210255, 2014, A1. Location in patent: Page/Page column 101
[2] Patent: WO2011/159857, 2011, A1. Location in patent: Page/Page column 201

4-bromo-1H-indole-7-carboxamide Preparation Products And Raw materials

Raw materials

Preparation Products

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