2-Bromo-5-chlorothiophene

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Names

[ CAS No. ]:
2873-18-9

[ Name ]:
2-Bromo-5-chlorothiophene

[Synonym ]:
2-brom-5-chlorthiophen
EINECS 220-708-5
Thiophene, 2-bromo-5-chloro-
2-chloro-5-bromothiophene
2-bromo-5-chloro thiophene
2-chloro-5-bromo thiophene
5-bromo-2-chlorothiophene
MFCD00014523
2-Bromo-5-chlorothiophene

Chemical & Physical Properties

[ Density]:
1.8±0.1 g/cm3

[ Boiling Point ]:
176.5±0.0 °C at 760 mmHg

[ Molecular Formula ]:
C4H2BrClS

[ Molecular Weight ]:
197.481

[ Flash Point ]:
85.0±0.0 °C

[ Exact Mass ]:
195.874908

[ PSA ]:
28.24000

[ LogP ]:
3.34

[ Vapour Pressure ]:
1.5±0.3 mmHg at 25°C

[ Index of Refraction ]:
1.612

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;half-mask respirator (US);multi-purpose combination respirator cartridge (US)

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
R20/21/22

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NA 1993 / PGIII

[ WGK Germany ]:
3

[ HS Code ]:
2934999090

Synthetic Route

Precursor & DownStream

Precursor

  • 2-Chlorothiophene
  • Bromothiophene

DownStream

  • 3-bromo-4-chlorothiophene
  • 5-Brom-3-chlorthiophen
  • 4-Bromo-2-chlorothiophene
  • 5-Chloro-2-thiophenecarbonitrile
  • thiophene-2,5-dicarbonitrile
  • 2-Chlorothiophene
  • 5,5'-dichloro-2,2'-bithiophene
  • 5-Chloro-2-thiophenecarboxylic acid
  • Ethyl5-chlorothiophene-2-carboxylate
  • 4-Ethoxyphenylboronic acid

Customs

[ HS Code ]: 2934999090

[ Summary ]:
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Electrochemical Reduction of Mono- and Dihalothiophenes at Carbon Cathodes in Dimethylformamide. First Example of an Electrolytically Induced Halogen Dance.

J. Org. Chem. 61(23) , 8074-8078, (1996)

Cyclic voltammetry and controlled-potential electrolysis have been employed to probe the electrochemical reduction of a number of mono- and dihalothiophenes at carbon cathodes in dimethylformamide con...

Photodissociation dynamics of halogenated thiophenes at 235 nm: a resonance enhanced multiphoton ionization-time-of-flight (REMPI-TOF) study.

J. Phys. Chem. A 116(44) , 10656-67, (2012)

The photodissociation dynamics of halogen-substituted thiophenes, namely, 2-chlorothiophene and 2-bromo-5-chlorothiophene, has been studied in a supersonic molecular beam around 235 nm, using resonanc...

Synthesis and Properties of Conjugated Polycarbosilanes with 1, 4-Bis (thiophene or phenylene)-buta-1, 3-diyne. Seo IK, et al.

Bull. Korean Chem. Soc. 20(6) , 677-82, (1999)


More Articles


Related Compounds

  • 2-bromo-5-(4-dimethoxy-2,6-dimethylphenyl)pyridine
  • 2-bromo-5-(methoxymethyl)-1,3,4-thiadiazole
  • 2-bromo-5-hydroxy-4-methoxy-benzonitrile
  • 2-bromo-5-methoxypyrimidine
  • 2-bromo-5-chloropentanoic acid
  • 2-BROMO-5-NITROBENZOTHIAZOLE
  • 1-(Oxan-4-yl)-4-prop-2-enoylpiperazin-2-one
  • N-[1-[(5-Fluoro-2-methoxyphenyl)methyl]cyclopropyl]prop-2-enamide
  • 5-Bromo-3-chloro-1,4-dimethylpyridin-2(1H)-one
  • 1-(4-Chloro-3-fluorophenyl)-2-phenoxyethan-1-amine
  • N-[(2,2-Difluorospiro[2.4]heptan-6-yl)methyl]prop-2-enamide
  • 3-Cyclopropyl-1-prop-2-enoylpyrrolidine-2-carboxylic acid
  • N-(1-Bromo-propylidene)-acetamidine
  • 4-[(2S)-2-aminopropyl]-3-methoxyphenol
  • 2-[(2-Chloro-1,2-difluoroethenyl)thio]propane
  • N-((2-(1,1-Dioxidoisothiazolidin-2-yl)cyclopentyl)methyl)acrylamide
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