C4H4BBrO2S
206.86 g/mol
Research ReagentWarning
5-Bromo-2-thiopheneboronic Acid (contains varying amounts of Anhydride)
CAS162607-17-2EC678-207-6
Category
Research Reagent
Compound Class
Heterocycle
Primary Use
Research Compound
5-Bromo-2-thiopheneboronic Acid is a research reagent employed as a boronic acid cross-coupling reagent. It is typically supplied with varying amounts of the corresponding anhydride and is used in laboratory-scale organic synthesis.
boronic acid cross-coupling reagent for research
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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CAS 162607-17-2
Related Compounds
ReferenceSame Category
5-Chlorothiophene-2-boronic acid
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research compound
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B-1-dibenzofuranylBoronic acid
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research compound
ReferenceSame Category
5-Methylthiophene-2-boronic acid
CAS162607-20-7
research compound
ReferenceSame Category
4-[[5-[[(2S)-1-[[(1S,2R,3S,5S,6S,16Z,18Z,20R,21S)-11-chloro-21-hydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8,23-dioxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.110,14.03,5]hexacosa-10,12,14(26),16,18-pentaen-6-yl]oxy]-1-oxopropan-2-yl]-methylamino]-2-methyl-5-oxopentan-2-yl]disulfanyl]-1-(2,5-dioxopyrrolidin-1-yl)oxy-1-oxobutane-2-sulfonic acid
CAS1626359-59-8
research compound
Safety Reference
Warning
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
Identifiers
IUPAC Name
(5-bromothiophen-2-yl)boronic acid
InChIKey
USJPOBDLWVCPGG-UHFFFAOYSA-N
SMILES
B(C1=CC=C(S1)Br)(O)O
Synonyms (10)
- 5-bromo-2-thienylboronic acid