3-Bromo-2-iodo-5-methylthiophene

Base Information

Chemical Name:3-Bromo-2-iodo-5-methylthiophene
CAS No.:89556-08-1
Molecular Formula:C5H4BrIS
Molecular Weight:302.961
Hs Code.:
DSSTox Substance ID:DTXSID30524264
Nikkaji Number:J3.583.728K
Wikidata:Q82390995

Synonyms:3-bromo-2-iodo-5-methylthiophene;89556-08-1;Thiophene, 3-bromo-2-iodo-5-methyl-;SCHEMBL20230333;DTXSID30524264

Suppliers and Price of 3-Bromo-2-iodo-5-methylthiophene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of 3-Bromo-2-iodo-5-methylthiophene

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:301.82618
Heavy Atom Count:8
Complexity:88.5

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=C(S1)I)Br

Technology Process of 3-Bromo-2-iodo-5-methylthiophene

There total 1 articles about 3-Bromo-2-iodo-5-methylthiophene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 95.0%

: 29421-92-9
4-bromo-2-methylthiophene

: 89556-08-1
3-bromo-2-iodo-5-methylthiophene

Guidance literature:: With N-iodo-succinimide; 2,2'-azobis(isobutyronitrile); acetic acid; In chloroform; at 50 ℃; for 3h;
DOI:10.3987/COM-08-11501

Reference yield: 94.0%

: 79887-09-5
(4-butylphenyl)acetylene

: 89556-08-1
3-bromo-2-iodo-5-methylthiophene

: 1135468-88-0
3-bromo-2-[2-(4-butylphenyl)ethynyl]-5-methylthiophene

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; diisopropylamine; In tetrahydrofuran; at 20 ℃; for 5h;
DOI:10.3987/COM-08-11501