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4-Bromothiophene-2-carbonitrile

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Products Intro: Product Name:4-bromothiophene-2-carbonitrile
CAS:18791-99-6
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CAS:18791-99-6
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CAS:18791-99-6
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4-Bromothiophene-2-carbonitrile manufacturers

4-Bromothiophene-2-carbonitrile Basic information
Product Name:4-Bromothiophene-2-carbonitrile
Synonyms:4-Bromo-2-cyanothiophene;4-Bromothiophene-2-carbonitrile;4-Bromothiophene-2-carbonitrile 98%;2-Thiophenecarbonitrile,4-broMo-;4-Bromothiophene-2-carbonitrile98%;4-Bromo-2-cyanothiophene >;4-Bromothiophene-2-carbonitrile ISO 9001:2015 REACH
CAS:18791-99-6
MF:C5H2BrNS
MW:188.05
EINECS:
Product Categories:blocks;Bromides;Carboxes;Heterocycles
Mol File:18791-99-6.mol
4-Bromothiophene-2-carbonitrile Structure
4-Bromothiophene-2-carbonitrile Chemical Properties
Melting point 47.0 to 51.0 °C
Boiling point 230.4±20.0 °C(Predicted)
density 1.82±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form powder to crystal
color White to Light yellow
Safety Information
Hazard Codes Xi,Xn
Risk Statements 22-37/38-41
Safety Statements 26-39
HazardClass IRRITANT
HS Code 2934999090
MSDS Information
4-Bromothiophene-2-carbonitrile Usage And Synthesis
Synthesis
4-Bromothiophene-2-carboxaldehyde

18791-75-8

4-Bromothiophene-2-carbonitrile

18791-99-6

The general procedure for the synthesis of 4-bromothiophene-2-carbonitrile from 4-bromo-2-thiophenecarboxaldehyde was as follows: 4-bromothiophene-2-carboxaldehyde (600 g, 3.14 mmol) and hydroxylamine hydrochloride (438 g, 6.30 mmol) were dissolved in pyridine (5 L). After the reaction mixture was cooled to room temperature, it was heated to 90 °C and maintained for 10 min. Subsequently, acetic anhydride (1940 g, 19.0 mmol) was slowly added dropwise and the reaction system was heated to 80°C for 1 hour. After completion of the reaction, the mixture was poured into water (20 L) and stirred for 30 min. After filtration and drying, the target product 4-bromothiophene-2-carbonitrile (564 g, 95% yield) was obtained.

References[1] Patent: CN104230960, 2017, B. Location in patent: Paragraph 0449; 0450; 0451
[2] Bioorganic and Medicinal Chemistry Letters, 2000, vol. 10, # 5, p. 415 - 418
[3] Bioorganic and Medicinal Chemistry Letters, 2005, vol. 15, # 11, p. 2870 - 2875
[4] Patent: US2017/151225, 2017, A1. Location in patent: Paragraph 0926; 0927
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