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BENZO[B]THIOPHENE-2-CARBONYL CHLORIDE

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BENZO[B]THIOPHENE-2-CARBONYL CHLORIDE Basic information

Product Name:
BENZO[B]THIOPHENE-2-CARBONYL CHLORIDE
Synonyms:
  • 1-Benzothiophene 2-carboxylic acid chloride
  • Benzo[b]thiophene-2-carboxylic acid chloride
  • Benzobüthiophene-2-carbonyl chloride, 98%
  • Benzo[b]thiophene-2-carbonyl chloride ,98%
  • 2-(Chlorocarbonyl)-1-benzothiophene, 1-Benzothiophene-2-carbonyl chloride
  • 1-Benzothiophene-2-carbonyl chloride
  • BENZO[B]THIOPHENE-2-CARBONYL CHLORIDE
  • BUTTPARK 98\04-18
CAS:
39827-11-7
MF:
C9H5ClOS
MW:
196.65
EINECS:
679-311-4
Product Categories:
  • Carbonyl Chlorides
  • Thiophenes & Benzothiophenes
  • Thiophenes & Benzothiophenes
  • ACIDHALIDE
  • Carbonyl Chlorides
Mol File:
39827-11-7.mol
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BENZO[B]THIOPHENE-2-CARBONYL CHLORIDE Chemical Properties

Melting point:
85-86°C
Boiling point:
176°C/17mmHg(lit.)
Density 
1.410±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
powder to crystal
color 
White to Orange to Green
Sensitive 
Moisture Sensitive
BRN 
125174
CAS DataBase Reference
39827-11-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C,Xi
Risk Statements 
34-36
Safety Statements 
26-36/37/39
RIDADR 
3261
Hazard Note 
Corrosive
HazardClass 
8
PackingGroup 
III
HS Code 
2934999090

MSDS

  • Language:English Provider:ALFA
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BENZO[B]THIOPHENE-2-CARBONYL CHLORIDE Usage And Synthesis

Synthesis

6314-28-9

39827-11-7

The general procedure for the synthesis of benz[b]thiophene-2-carboxylic acid from benz[b]thiophene-2-carboxylic acid was as follows: benz[b]thiophene-2-carboxylic acid (356.42 mg, 2 mmol) was suspended in anhydrous toluene (6 mL) and thionyl chloride (4.4 mL, 60 mmol) and N,N-dimethylformamide (DMF, 0.05 mL) were added. After stirring at room temperature, the mixture was heated to reflux for 8 hours. Upon completion of the reaction, the volatiles were removed under reduced pressure to afford benzo[b]thiophene-2-carbonyl chloride as a yellow powder. Purification by rapid chromatography on silica gel using ethyl acetate/hexane (1:9, v/v) as eluent gave the target product (393.64 mg, 94.9% yield) as a white powder. The spectral data of the product were in agreement with those reported in the literature.1H NMR (300 MHz, CDCl3): δ 8.31 (s, 1H), 7.04-7.89 (m, 2H), 7.60-7.46 (m, 2H); 13C NMR (300 MHz, CDCl3): δ 161.14, 144.07, 138.05, 136.59, 135.89, 128.75, 126.68, 125.66, 122.91.

References

[1] Journal of the American Chemical Society, 2011, vol. 133, # 11, p. 3764 - 3767
[2] Patent: WO2012/99785, 2012, A2. Location in patent: Page/Page column 25
[3] Tetrahedron Asymmetry, 2003, vol. 14, # 3, p. 339 - 346
[4] Organometallics, 2015, vol. 34, # 12, p. 3065 - 3071
[5] Journal of the American Chemical Society, 2005, vol. 127, # 43, p. 15010 - 15011

BENZO[B]THIOPHENE-2-CARBONYL CHLORIDE Preparation Products And Raw materials

Raw materials

BENZO[B]THIOPHENE-2-CARBONYL CHLORIDESupplier

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