2,5-Dibromothiophene CAS 3141-27-3

Introduction:Basic information about 2,5-Dibromothiophene CAS 3141-27-3, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

2,5-Dibromothiophene Basic information

Product Name:2,5-Dibromothiophene
Synonyms:Thiophene,2,5-dibromo-;2,5-DIBROMO THIOPHENE 98.0%MIN;TH-2Bra;2,5-Dibromthiophen;2,5-DibroMothiophene, 95% 25GR;2,5-Dibromothiophene,95%;alpha,alpha-Dibromothiophene;NSC 4488
CAS:3141-27-3
MF:C4H2Br2S
MW:241.93
EINECS:221-547-3
Product Categories:Sulphur Derivatives;Thiophene&Benzothiophene;Thiophenes;Metal Isotopes;Thiophens;Sulfur & Selenium Compounds;Halogenated Heterocycles;Heterocyclic Building Blocks;ThiophenesBuilding Blocks;Heterocycle-oher series;bc0001
Mol File:3141-27-3.mol

2,5-Dibromothiophene Chemical Properties

Melting point -6 °C (lit.)
Boiling point 211 °C (lit.)
density 2.147 g/mL at 25 °C (lit.)
refractive index 1.627-1.63
Fp 99 °C
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform, Methanol
form Liquid
color Clear pale yellow to brown
Specific Gravity2.147
Water Solubility practically insoluble
BRN 109899
InChI1S/C4H2Br2S/c5-3-1-2-4(6)7-3/h1-2H
InChIKeyKBVDUUXRXJTAJC-UHFFFAOYSA-N
SMILESBrc1ccc(Br)s1
CAS DataBase Reference3141-27-3(CAS DataBase Reference)
NIST Chemistry ReferenceThiophene, 2,5-dibromo-(3141-27-3)
EPA Substance Registry SystemThiophene, 2,5-dibromo- (3141-27-3)

Safety Information

Hazard Codes T+,Xi
Risk Statements 68-43-36/37/38-28-20/21
Safety Statements 45-36/37/39-28A-26-36
RIDADR UN2810
WGK Germany 3
Hazard Note Irritant
TSCA TSCA listed
HazardClass 6.1
PackingGroup II
HS Code 29349990
Storage Class10 - Combustible liquids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3

2,5-Dibromothiophene Usage And Synthesis

Chemical PropertiesLight Yellow Liquid
Uses2,5-Dibromothiophene, is mainly used as pharmaceutical intermediate and synthesis intermediate.
Uses2,5-Dibromothiophene was used as starting reagent for the synthesis of α,α′-didecylquater-, -quinque- and -sexi-thiophenes. It was used in the preparation of soluble α,ω-diformyl-a-oligothiophenes.
Synthesis Reference(s)The Journal of Organic Chemistry, 58, p. 3072, 1993 DOI: 10.1021/jo00063a028
Synthesis, p. 890, 1988 DOI: 10.1055/s-1988-27740
General Description2,5-Dibromothiophene polymerizes by debromination with magnesium catalyzed by nickel compounds to form poly(2,5- thienylene) .
References[1] Tetrahedron Letters, 2010, vol. 51, # 1, p. 205 - 208
[2] Journal of Organic Chemistry, 1993, vol. 58, # 11, p. 3072 - 3075
[3] Synthesis, 1988, # 11, p. 890 - 891
[4] Journal of Organic Chemistry, 2018, vol. 83, # 2, p. 930 - 938
[5] Patent: KR2018/17709, 2018, A. Location in patent: Paragraph 0173; 0176-0179

2,5-Dibromothiophene Preparation Products And Raw materials

Raw materialsThiophene(SIV) (9CI)-->Potassium tert-butoxide-->Chloroform-->2,5-BIS(TRIMETHYLSILYL)THIOPHENE-->N-Bromosuccinimide-->Acetic acid-->AKOS 92422-->Thiophene, 2,5-dibromo-3-fluoro-
Preparation Products5-Bromothiophene-2-carbohydrazide-->3,4-DIAMINOTHIOPHENE DIHYDROCHLORIDE-->Ethyl 5-bromothiophene-2-carboxylate-->5,5'-Dibromo-2,2'-bithiophene-->ETHYL 5-BROMOTHIOPHENE-2-CARBOXYLATE-->2,2':5',2''-TERTHIOPHENE-->2,3,5-Tribromothiophene-->2-Acetyl-5-bromothiophene-->Thiophene-2,5-dicarbonitrile-->3,5-DIBROMO-2-METHYLTHIOPHENE-->2-(TRIBUTYLSTANNYL)THIOPHENE-->5-Bromothiophenesulfonyl chloride-->5-Bromo-2-thiophenecarboxylic acid
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