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2,4-Dibromothiophene

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2,4-Dibromothiophene manufacturers

2,4-Dibromothiophene Basic information
Product Name:2,4-Dibromothiophene
Synonyms:2,4-DIBROMOTHIOPHENE;2,4-Dibromothiophene,94%;2,4-DIBROMOTHIOPHENE, 90+%;2,4-DIBROMOTHIOPHENE 96%;2,4-DIBROMOTHIOPHENE,96%;2,4-Dibromothiophene>;Thiophene, 2,4-dibromo-;2,4-Dibromothiophene ISO 9001:2015 REACH
CAS:3140-92-9
MF:C4H2Br2S
MW:241.93
EINECS:678-717-9
Product Categories:Heterocycle-oher series;Thiophene&Benzothiophene;Thiophens
Mol File:3140-92-9.mol
2,4-Dibromothiophene Structure
2,4-Dibromothiophene Chemical Properties
Melting point -26.3°C
Boiling point 215°C
density 2.157 g/mL at 25 °C
refractive index 1.631-1.633
Fp 215°C
storage temp. Keep in dark place,Inert atmosphere,2-8°C
form liquid
Specific Gravity2.149
color Colorless to Light yellow to Light orange
Water Solubility It is insoluble in water.
BRN 107651
InChIInChI=1S/C4H2Br2S/c5-3-1-4(6)7-2-3/h1-2H
InChIKeyWAQFYSJKIRRXLP-UHFFFAOYSA-N
SMILESC1(Br)SC=C(Br)C=1
CAS DataBase Reference3140-92-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi,T
Risk Statements 36/37/38-20/21/22-41-37/38-25
Safety Statements 36/37/39-26-36-45-39
RIDADR UN2810
WGK Germany 3
Hazard Note Irritant
HazardClass 6.1
PackingGroup III
HS Code 29349990
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 3 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
2,4-Dibromothiophene English
ACROS English
ALFA English
2,4-Dibromothiophene Usage And Synthesis
Chemical Propertiesclear colorless to light brown liquid
Uses2,4-Dibromothiophene is used as an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. It is also used as an intermediate in organic synthesis.
Synthesis2,3,5-Tribromothiophene (1):

120 g (1.43 mol) of thiophene was added to 240 mL of glacial acetic acid and 687 g (4.30 mol) of Br2 was added dropwise at 5-10 C, stirred at room temperature for 3 h and heated at reflux for 2 h. The residue was then evaporated under vacuum and distilled through a short Vigreux column. Subsequently, the glacial acetic acid was evaporated under vacuum and the residue was distilled through a short Vigreux column under water jet vacuum. Yield: 376.2 g (1.17 mol)1 (82%).

2,4-Dibromothiophene (4):

120 g (0.374 mol) of 2,3,5-tribromothiophene (1) was dissolved in 300 mL of ether, cooled to -30 C under N2, and 234 mL of a n-hexane solution of 6NBuLi (0.374 mol) was added dropwise over a period of 10 min at this temperature, stirred at -30 C for 5 minutes, poured into 1 L of cold water and extracted with ether 3 times. The combined ether phases were washed three times with water, dried with Na2SO4 and evaporated. The residue was fractionated on a 1 mVigreux flask under vacuum. Yield: 60 g (0.248 mol)4 (66%).

2,4-Dibromothiophene Preparation Products And Raw materials
Raw materialsDiethyl ether-->n-Butyllithium-->2,3,5-Tribromothiophene
Preparation Products2,3-Dibromothiophene-->3-Bromothiophene-->4-Bromothiophene-2-carboxaldehyde-->4-Bromo-2-(methylthio)thiophene
Tag:2,4-Dibromothiophene(3140-92-9) Related Product Information
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