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3-Bromothiophene-2-carboxaldehyde diethyl acetal is a chemical compound that serves as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is a derivative of 3-bromothiophene, a heterocyclic compound with a sulfur atom in its five-membered ring. The presence of the diethyl acetal group in the molecule enhances its stability and makes it more suitable for various chemical reactions.

34042-95-0

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34042-95-0 Usage

Uses

Used in Pharmaceutical Industry:
3-Bromothiophene-2-carboxaldehyde diethyl acetal is used as a key intermediate in the synthesis of drugs. Its unique chemical properties and versatile nature allow it to be incorporated into the development of a wide range of pharmaceutical products.
Used in Agrochemical Industry:
3-Bromothiophene-2-carboxaldehyde diethyl acetal is also used as an intermediate in the production of agrochemicals, such as pesticides and dyes. Its stability and reactivity make it a valuable component in the creation of these products, contributing to their effectiveness and performance.

Check Digit Verification of cas no

The CAS Registry Mumber 34042-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,0,4 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 34042-95:
(7*3)+(6*4)+(5*0)+(4*4)+(3*2)+(2*9)+(1*5)=90
90 % 10 = 0
So 34042-95-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H13BrO2S/c1-3-11-9(12-4-2)8-7(10)5-6-13-8/h5-6,9H,3-4H2,1-2H3

34042-95-0 Well-known Company Product Price

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  • Alfa Aesar

  • (L19397)  3-Bromothiophene-2-carboxaldehyde diethyl acetal, 97%   

  • 34042-95-0

  • 1g

  • 423.0CNY

  • Detail
  • Alfa Aesar

  • (L19397)  3-Bromothiophene-2-carboxaldehyde diethyl acetal, 97%   

  • 34042-95-0

  • 5g

  • 1527.0CNY

  • Detail

34042-95-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-2-(diethoxymethyl)thiophene

1.2 Other means of identification

Product number -
Other names 3-Bromothiophene-2-Carboxaldehyde Diethyl Acetal

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:34042-95-0 SDS

34042-95-0Relevant academic research and scientific papers

Regiocontrolled Halogen Dance of Bromothiophenes and Bromofurans

Mari, Daichi,Miyagawa, Naoki,Okano, Kentaro,Mori, Atsunori

, p. 14126 - 14137 (2018/11/23)

The LDA (lithium diisopropylamide)-promoted regiocontrolled halogen dance of α-bromothiophenes and α-bromofurans is described. Bromothiophenes bearing a diethyl acetal moiety undergo selective deprotonation at the β-position adjacent to the bromo group. In contrast, oxazoline, ester, and amide groups act as directing groups in the initial lithiation step to generate a carbanion at the β-position neighboring the directing group to exclusively give the other regioisomer. These results can be applied to the regiocontrolled halogen dance of bromofuran derivatives.

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