67768-63-2 Usage
General Description
Methyl 2-methoxycyclohexa-2,5-diene-1-carboxylate is a chemical compound with the molecular formula C10H12O3. It is a colorless liquid that is commonly used in the synthesis of organic compounds. methyl 2-methoxycyclohexa-2,5-diene-1-carboxylate is often utilized in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Methyl 2-methoxycyclohexa-2,5-diene-1-carboxylate has various industrial applications, including its use as a flavor and fragrance ingredient. It is known for its sweet, fruity aroma and is frequently used in the manufacturing of perfumes, soaps, and other personal care products. Additionally, it is a valuable intermediate in the creation of complex organic molecules for a wide range of commercial purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 67768-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,7,6 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 67768-63:
(7*6)+(6*7)+(5*7)+(4*6)+(3*8)+(2*6)+(1*3)=182
182 % 10 = 2
So 67768-63-2 is a valid CAS Registry Number.
67768-63-2Relevant articles and documents
A mild and effective method for the transesterification of carboxylic acid esters
Baumhof, Patrick,Mazitschek, Ralph,Giannis, Athanassios
, p. 3672 - 3674 (2007/10/03)
An extraordinarily versatile transesterification of simple or highly functionalized esters of aliphatic and aromatic carboxylic acids in high yields is catalyzed by dibutyltin oxide [Eq. (1)]. The reaction is compatible with several functional groups, for example, acetals, ketals, aliphatic bromides, enol ethers, urethanes, as well as free hydroxy, phenolic, and amino groups, and even with water.
AN ECONOMICAL DIELS-ALDER STRATEGY FOR THE SYNTHESIS OF DAPHNIPHYLLUM ALKALOIDS
Orban, John,Turner, John V.
, p. 2697 - 2700 (2007/10/02)
A convergent and essentially self-consistent strategy, featuring an unusual Diels-Alder reaction has been devised for the stereo-controlled synthesis of a logical tetracyclic precursor 21 to daphniphyllum alkaloids.
