56674-63-6 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
(2E)-3-methoxy-2-methylprop-2-enoic acid is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and reactivity allow for the development of new and effective compounds for medical and agricultural applications.
Used in Organic Chemistry Research:
As a versatile building block, (2E)-3-methoxy-2-methylprop-2-enoic acid is used in organic chemistry research to explore new synthetic pathways and develop innovative chemical reactions. Its ability to participate in esterification, oxidation, and reduction reactions makes it a valuable tool for advancing the field of organic chemistry.
Used in Flavor and Fragrance Production:
(2E)-3-methoxy-2-methylprop-2-enoic acid is also used as a starting material for the production of various flavors and fragrances in the food and cosmetic industries. Its unique chemical properties contribute to the creation of distinct and appealing scents and tastes, enhancing the sensory experience of consumer products.
Check Digit Verification of cas no
The CAS Registry Mumber 56674-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,7 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56674-63:
(7*5)+(6*6)+(5*6)+(4*7)+(3*4)+(2*6)+(1*3)=156
156 % 10 = 6
So 56674-63-6 is a valid CAS Registry Number.
56674-63-6Relevant academic research and scientific papers
Synthesis of racemic carbocyclic cyclopropanoid nucleoside analogues
Csuk, Rene,Von Scholz, Yvonne
, p. 7193 - 7206 (2007/10/02)
As further representatives of a novel class of carbocyclic nucleoside analogues (±)-cis- and (±)-trans-(2-hydroxymethylcyclopropyl)-uracil, -thymine, and -inosine were synthesized from the corresponding dialkyl 1,2-cyclopropane dicarboxylates.
DICHLOROMETHYL ALKYL ETHERS AND SULFIDES IN THE REFORMATSKII REACTION
Lapkin, I. I.,Fotin, V. V.
, p. 659 - 663 (2007/10/02)
A study was carried out on the reaction of dichloromethyl alkyl ethers and sulfides with α-brominated esters in the presence of zinc resulting in the formation of either α-alkyl-β-alkoxyacrylates (or α-alkyl-β-alkylthioacrylates) or α,α,α',α'-tetramethyl-β-alkoxyglutaric acid ( or α,α,α',α'-tetramethyl-β-alkylthioglutaric acid) depending on the structure of the starting bromoester.PMR and IR spectroscopy indicates the geometry of the α-alkyl-β-alkoxyacrylates and α-alkyl-β-alkylthioacrylates.
