4-BROMO-2-THIOPHENECARBOXAMIDE

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Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:4-Bromothiophene-2-carboxamide
CAS:83933-17-9
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-65210
Company Name: Aladdin Scientific
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Products Intro: Product Name:4-Bromothiophene-2-carboxamide
CAS:83933-17-9
Purity:98% Package:$43.9/250mg;$133.9/1g;$598.9/5g;Bulk package Remarks:98%
Company Name: Amadis Chemical Company Limited
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Products Intro: Product Name:4-Bromothiophene-2-carboxamide
CAS:83933-17-9
Purity:0.97 Package:mgs,gs,kgs Remarks:A864196
Company Name: J & K SCIENTIFIC LTD.  
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Products Intro: Product Name:4-bromo-2-thiophenecarboxamide(SALTDATA: FREE)
CAS:83933-17-9
Purity:95% Package:1G, 5G, 10G, 25G
Company Name: Energy Chemical  
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Products Intro: Product Name:4-BroMothiophene-2-carboxaMide
CAS:83933-17-9
Purity:98% Package:1g,5g
4-BROMO-2-THIOPHENECARBOXAMIDE Basic information
Product Name:4-BROMO-2-THIOPHENECARBOXAMIDE
Synonyms:4-BROMO-2-THIOPHENECARBOXAMIDE;2-thiophenecarboxamide, 4-bromo-;4-bromo-2-thiophenecarboxamide(SALTDATA: FREE);4-bromothiophene-2-carboxamide
CAS:83933-17-9
MF:C5H4BrNOS
MW:206.06
EINECS:
Product Categories:
Mol File:83933-17-9.mol
4-BROMO-2-THIOPHENECARBOXAMIDE Structure
4-BROMO-2-THIOPHENECARBOXAMIDE Chemical Properties
storage temp. Keep in dark place,Sealed in dry,Room Temperature
AppearanceWhite to off-white Solid
Safety Information
Risk Statements 43
Safety Statements 36/37
HazardClass IRRITANT
MSDS Information
4-BROMO-2-THIOPHENECARBOXAMIDE Usage And Synthesis
Synthesis
4-BROMO-THIOPHENE-2-CARBALDEHYDE OXIME

31767-01-8

4-BROMO-2-THIOPHENECARBOXAMIDE

83933-17-9

The general procedure for the synthesis of 4-bromothiophene-2-carboxamide from the compound (CAS: 31767-01-8) is as follows: in a 25 mL round-bottomed flask equipped with a magnetic stirrer, aldoxime (5 mmol), copper(II) acetate (45 mg, 0.25 mmol), acetonitrile (10 mg, 0.25 mmol), and ethanol (15 mL) were added in sequence. The reaction mixture was stirred for 4-8 hours at 78 °C or 12 hours at room temperature. After completion of the reaction, the solvent was removed by rotary evaporator. The crude product was purified by column chromatography to afford the target compound 4-bromothiophene-2-carboxamide.

References[1] RSC Advances, 2016, vol. 6, # 43, p. 37093 - 37098
[2] Journal of Chemical Research, 2016, vol. 40, # 10, p. 594 - 596
[3] Bulletin de la Societe Chimique de France, 1967, p. 4115 - 4120
4-BROMO-2-THIOPHENECARBOXAMIDE Preparation Products And Raw materials
Raw materials4-BROMO-THIOPHENE-2-CARBALDEHYDE OXIME-->4-Bromo-2-thiophenecarboxylic acid-->4-Bromothiophene-2-carboxaldehyde-->Acetonitrile-->Ethanol-->Copper(II) acetate
Preparation Products4-Bromothiophene-2-carbonitrile
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