46029-22-5 Usage
Uses
Used in Pharmaceutical Industry:
5-Methylthiophene-2,3-dicarboxylic Acid is used as a key intermediate in the synthesis of various pharmaceuticals for its unique chemical structure and reactivity. It plays a crucial role in the development of new drugs, contributing to the advancement of medical treatments.
Used in Agrochemical Industry:
5-Methylthiophene-2,3-dicarboxylic Acid is also utilized as a building block in the creation of agrochemicals, which are essential for enhancing crop protection and agricultural productivity. Its unique properties make it a valuable component in the formulation of effective and innovative agrochemical products.
Used in Material Science:
5-Methylthiophene-2,3-dicarboxylic Acid is employed in the development of new materials, such as polymers and composites, due to its versatile chemical reactivity. This allows for the creation of materials with improved properties and performance, catering to various industrial needs.
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.
46029-22-5Relevant academic research and scientific papers
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.
