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3,4-DIBROMOTHIOPHEN-2-YLBORONIC ACID is a boronic acid derivative with the molecular formula C4H4BBr2O2S. It features a thiophene ring with two bromine atoms attached at the 3 and 4 positions, making it a versatile reagent in organic synthesis and pharmaceutical research.

1256355-38-0

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1256355-38-0 Usage

Uses

Used in Organic Synthesis:
3,4-DIBROMOTHIOPHEN-2-YLBORONIC ACID is used as a reagent for the formation of carbon-carbon and carbon-heteroatom bonds. Its versatile reactivity and functional group compatibility make it a valuable tool in the development of new molecules and materials.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3,4-DIBROMOTHIOPHEN-2-YLBORONIC ACID is used as a building block for the synthesis of bioactive compounds. Its unique structure and reactivity contribute to the discovery and development of new drugs with potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1256355-38-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,3,5 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1256355-38:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*5)+(3*5)+(2*3)+(1*8)=160
160 % 10 = 0
So 1256355-38-0 is a valid CAS Registry Number.

1256355-38-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3,4-dibromothiophen-2-yl)boronic acid

1.2 Other means of identification

Product number -
Other names 3,4-Dibromothiophene-2-boronic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1256355-38-0 SDS

1256355-38-0Upstream product

1256355-38-0Downstream Products

1256355-38-0Relevant academic research and scientific papers

Preparation of brominated 2-alkoxythiophenes via oxidation and etherification of 2-thienyltrifluoroborate salts

Tietz, Jonathan I.,Seed, Alexander J.,Sampson, Paul

supporting information, p. 5058 - 5061 (2013/01/15)

The synthesis of ring brominated long-chain 2-alkoxythiophenes is reported, involving mild (Oxone) oxidation of readily prepared 2-thienyltrifluoroborate salts followed by Mitsunobu etherification. Both procedures are operationally straightforward and use inexpensive reagents. Using this approach, several novel mono- and dibrominated octyloxythiophenes with previously elusive substitution patterns were prepared. One such compound was elaborated to a novel 5-alkoxythieno[3,2-b]thiophene-2-carboxylate ester, marking the first synthetic entry into this family of compounds.

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