1002-64-8 Usage
General Description
(2E,8E)-2,8-Decadiene-4,6-diyn-1-ol acetate is a chemical compound with a long, specific name that is commonly used in the field of organic chemistry. It is an acetate ester derivative of a diynol compound, which means it is likely used as a solvent or in the synthesis of other organic molecules. The presence of diene and diyn functional groups in the compound suggests it may have applications in organic synthesis reactions, as these functional groups are often involved in cross-coupling reactions and other types of chemical transformations. The compound may also have potential applications in the field of materials science, as diyn-containing compounds are known to have interesting physical and electronic properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1002-64-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1002-64:
(6*1)+(5*0)+(4*0)+(3*2)+(2*6)+(1*4)=28
28 % 10 = 8
So 1002-64-8 is a valid CAS Registry Number.
1002-64-8Relevant articles and documents
STEREOCONTROLLED SYNTHESIS OF NATURALLY-OCCURRING POLYACETYLENES CHARACTERIZED BY (E)-1-EN-3-YNE, (E)-1-EN-3,5-DIYNE, (1E,5E)-1,5-DIEN-3-YNE, AND (1E,7E)-1,7-DIEN-3,5-DIYNE MOIETIES
Carpita, Adriano,Neri, Dario,Rossi, Renzo
, p. 481 - 490 (2007/10/02)
A stereocontrolled synthesis of five naturally-occurring polyacetylenes, i.e. methyl (E)-5-(2-thienyl)-2-penten-4-ynoate, 9, (E)-N-methyl-N-(2-methylpropyl)-2-decen-4,6-diynamide, 10, (E)-1-(3-methyl-2-butenoyloxy)-2-decen-4,6-diyne, 11, (2E,6E)-1-acetoxy-2,6-decadien-4-yne, 12, and (2E,8E)-1-acetoxy-2,8-decadien-4,6-diyne, 13, is reported.The flexible strategy involves palladium(0)-copper(I) catalyzed coupling reactions to construct the carbon skeleton of the target molecules and to prepare an important C5 building block, i.e. (E)-2-penten-4-yn-1-ol, 21.This compound is also an useful intermediate to lipoxins A and B.A highly diastereoselective palladium-catalyzed carbon-carbon bond forming reaction, recently developed in our laboratory, has been used in a key synthetic step to compound 12.
