3-Bromothiophene

3-Bromothiophene is an organosulfur compound with the formula C4H3BrS. It is a colorless liquid. It is a precursor to the antibiotic timentin and the vasodilator cetiedil.[1]

3-Bromothiophene
Names
Preferred IUPAC name
3-Bromothiophene
Other names
3-Thienyl bromide, 3BT
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.011.656
EC Number
  • 212-821-3
UNII
Properties
C4H3BrS
Molar mass 163.03 g·mol−1
Appearance Colorless liquid
Density 1.74 g/mL
Melting point −10 °C (14 °F; 263 K)
Boiling point 150–158 °C (302–316 °F; 423–431 K)
Immiscible
Hazards
Main hazards N,Xi,Xn,T
GHS pictograms
GHS Signal word Danger
GHS hazard statements
H226, H301, H310, H310, H315, H317, H319, H330, H335, H411
P210, P233, P240, P241, P242, P243, P260, P261, P262, P264, P270, P271, P272, P273, P280, P284, P301+310, P302+350, P302+352, P303+361+353, P304+340, P305+351+338, P310, P312, P320
Flash point 56 °C (133 °F; 329 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Preparation

Unlike 2-bromothiophene, the 3-bromo isomer cannot be prepared directly from thiophene. It can be prepared by debromination of 2,3,5-tribromothiophene,[2] which is obtained by bromination of thiophene.

Synthese van 3-broomthiofeen

See also

References

  1. Jonathan Swanston (2006). "Thiophene". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a26_793.pub2.
  2. S. Gronowitz (1959). "3-Bromothiophene". Org. Syntheses. 44: 9. doi:10.15227/orgsyn.044.0009.
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