Basic information Safety Supplier Related

(4-BROMO-2-THIENYL)METHANOL

Basic information Safety Supplier Related

(4-BROMO-2-THIENYL)METHANOL Basic information

Product Name:
(4-BROMO-2-THIENYL)METHANOL
Synonyms:
  • 4-BROMO-2-(HYDROXYMETHYL)THIOPHENE
  • (4-BROMO-2-THIENYL)METHANOL
  • RARECHEM AL BD 0179
  • (4-BroMothien-2-yl)Methanol
  • 2-Thiophenemethanol, 4-bromo-
  • 4-Bromothiophene-2-methanol
  • 4-Bromo-2-thiophenemethanol
CAS:
79757-77-0
MF:
C5H5BrOS
MW:
193.06
Product Categories:
  • Building Blocks
  • Thiophene
Mol File:
79757-77-0.mol
More
Less

(4-BROMO-2-THIENYL)METHANOL Chemical Properties

Melting point:
30 °C
Boiling point:
271.5±25.0 °C(Predicted)
Density 
1.772±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
solubility 
soluble in Methanol
form 
powder to lump
pka
13.50±0.10(Predicted)
color 
White to Orange to Green
More
Less

Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22-36/37/38-41-22
Safety Statements 
26-36/37/39-39
HS Code 
2934999090
More
Less

(4-BROMO-2-THIENYL)METHANOL Usage And Synthesis

Synthesis

18791-75-8

79757-77-0

Step I: Sodium borohydride (5.20 g, 0.137 mol) was added batchwise to a solution of 4-bromo-2-thiophenecarboxaldehyde (25.0 g, 0.131 mol) in anhydrous tetrahydrofuran (400 mL). The reaction mixture was stirred at room temperature for 1.5 hours. Upon completion of the reaction, saturated ammonium chloride solution (100 mL) was slowly added to quench the reaction. Subsequently, the reaction mixture was extracted with ethyl acetate and the organic phases were combined and washed with saturated brine. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford (4-bromo-2-thienyl)methanol (25.02 g, 99% yield), and the product could be used for subsequent reactions without further purification. NMR hydrogen spectrum (400 MHz, CDCl3): δ = 1.93 (broad single peak, 1H), 4.79 (single peak, 2H), 6.93 (single peak, 1H), 7.18 (double peak, J = 1.5 Hz, 1H).

References

[1] Journal of the American Chemical Society, 2007, vol. 129, # 24, p. 7523 - 7530
[2] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 4, p. 1788 - 1792
[3] Synthesis, 1983, # 1, p. 73 - 75
[4] Patent: WO2013/110643, 2013, A1. Location in patent: Paragraph 00212; 00213
[5] Bioorganic and Medicinal Chemistry, 2008, vol. 16, # 4, p. 1992 - 2010

(4-BROMO-2-THIENYL)METHANOLSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Email
sales@chemwish.com
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Email
chenyj@titansci.com
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com