ChemicalBook > CAS DataBase List > 6-BroMoquinoline-3-carboxaMide

6-BroMoquinoline-3-carboxaMide

Product Name
6-BroMoquinoline-3-carboxaMide
CAS No.
1296950-96-3
Chemical Name
6-BroMoquinoline-3-carboxaMide
Synonyms
6-BroMoquinoline-3-carboxaMide;3-Quinolinecarboxamide, 6-bromo-
CBNumber
CB92735888
Molecular Formula
C10H7BrN2O
Formula Weight
251.08
MOL File
1296950-96-3.mol
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6-BroMoquinoline-3-carboxaMide Property

Boiling point:
471.9±25.0 °C(Predicted)
Density 
1.655±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
14.85±0.30(Predicted)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H332Harmful if inhaled

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

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

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Crysdot
Product number
CD11298480
Product name
6-Bromoquinoline-3-carboxamide
Purity
97%
Packaging
250mg
Price
$244
Updated
2021/12/16
Chemenu
Product number
CM142965
Product name
6-bromoquinoline-3-carboxamide
Purity
97%
Packaging
1g
Price
$574
Updated
2021/12/16
Crysdot
Product number
CD11298480
Product name
6-Bromoquinoline-3-carboxamide
Purity
97%
Packaging
1g
Price
$608
Updated
2021/12/16
Alichem
Product number
1296950963
Product name
6-Bromoquinoline-3-carboxamide
Packaging
1g
Price
$646.8
Updated
2021/12/16
Chemenu
Product number
CM142965
Product name
6-bromoquinoline-3-carboxamide
Purity
97%
Packaging
5g
Price
$1427
Updated
2021/12/16
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6-BroMoquinoline-3-carboxaMide Chemical Properties,Usage,Production

Synthesis

798545-30-9

1296950-96-3

General procedure for the synthesis of 6-bromoquinoline-3-carboxamide from 6-bromoquinoline-3-carboxylic acid: Step 1: To a suspension of 6-bromoquinoline-3-carboxylic acid (0.50 g, 1.98 mmol) in dichloromethane (10 ml) was slowly added oxalyl chloride (327 mg, 0.22 ml, 2.58 mmol) followed by dropwise addition of DMF (3 drops). Mild gas escape was observed during the reaction. The reaction mixture was stirred at room temperature for 2 h and subsequently concentrated by rotary evaporation to give a white solid. The residue was resuspended in ether (10 ml) and 28% aqueous ammonium hydroxide solution (2.0 ml, 16.0 mmol) was slowly added. The mixture was stirred vigorously at room temperature for 2 h. After completion of the reaction, the precipitate was collected by filtration and washed sequentially with water and ether. The product was dried under high vacuum to give 457 mg (92% yield) of 6-bromoquinoline-3-carboxamide as a beige solid.

References

[1] Patent: WO2014/86697, 2014, A1. Location in patent: Page/Page column 44-45

6-BroMoquinoline-3-carboxaMide Preparation Products And Raw materials

Raw materials

Preparation Products

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6-BroMoquinoline-3-carboxaMide Suppliers

Aladdin Scientific
Tel
Email
tp@aladdinsci.com
Country
United States
ProdList
52923
Advantage
58
Synthonix Inc
Tel
--
Fax
--
Email
info@synthonix.com
Country
United States
ProdList
6872
Advantage
58
Combi-Blocks Inc.
Tel
--
Fax
--
Email
sales@combi-blocks.com
Country
United States
ProdList
6618
Advantage
69

1296950-96-3, 6-BroMoquinoline-3-carboxaMideRelated Search:


  • 6-BroMoquinoline-3-carboxaMide
  • 3-Quinolinecarboxamide, 6-bromo-
  • 1296950-96-3