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46029-22-5

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46029-22-5 Usage

General Description

5-Methylthiophene-2,3-dicarboxylic acid is an organic compound with the chemical formula C7H6O4S. It is a derivative of thiophene, a five-membered heterocyclic compound containing sulfur. 5-Methylthiophene-2,3-dicarboxylic Acid is used in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical structure and reactivity. It has potential applications in the development of new drugs and materials. 5-Methylthiophene-2,3-dicarboxylic acid is of interest to researchers and industries looking to develop new and innovative products.

Check Digit Verification of cas no

The CAS Registry Mumber 46029-22-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,0,2 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 46029-22:
(7*4)+(6*6)+(5*0)+(4*2)+(3*9)+(2*2)+(1*2)=105
105 % 10 = 5
So 46029-22-5 is a valid CAS Registry Number.

46029-22-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methylthiophene-2,3-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names QC-5992

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:46029-22-5 SDS

46029-22-5Downstream Products

46029-22-5Relevant articles and documents

Stereoselective synthesis of thiophenedimethyl- and benzenedimethyl- α,α′-bridged bis(glycines)

Hammer, Kristin,Benneche, Tore,Hope, Hakon,Undheim, Kjell

, p. 392 - 402 (2007/10/03)

Conformationally constrained cystine analogues have been synthesized which have an all-carbon backbone-chain as a bridge between the α,α′-positions in two glycine units. An aromatic ring consisting of a 1,2-disubstituted benzene or a 2,3- and 2,5-disubstituted thiophene has been inserted into the bridge. Chiral auxiliaries were used to effect stereoselective syntheses of the (S,S)-bis(amino acids). The latter were further derivatized as Fmoc-derivatives suitable for peptide syntheses. The product 2,3-bis[(2A,5S)-(2,5-dihydro-3,6-dimethoxy-2-isopropyl-5-pyrazinyl)methyl]-5- methylthiophene has been subjected to X-ray analysis. Acta Chemica Scandinavica 1997.

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