10562-68-2 Usage
Uses
Used in Organic Synthesis:
4-ETHYNYL-2,6-DIMETHYL-4-HEPTANOL is used as a reagent in organic synthesis for its unique structure and reactivity, enabling the creation of a variety of complex organic molecules.
Used in Chemical Reactions:
As an intermediate in chemical reactions, 4-ETHYNYL-2,6-DIMETHYL-4-HEPTANOL facilitates the synthesis of other compounds, contributing to the advancement of chemical research and development.
Used in Pharmaceutical Industry:
4-ETHYNYL-2,6-DIMETHYL-4-HEPTANOL is used as a building block in the development of pharmaceuticals, potentially leading to the discovery of new drugs and therapeutic agents.
Used in Biochemistry:
In biochemistry, 4-ETHYNYL-2,6-DIMETHYL-4-HEPTANOL is employed as a reagent in various biochemical assays and processes, contributing to a better understanding of biological systems.
Used in Material Science:
4-ETHYNYL-2,6-DIMETHYL-4-HEPTANOL is utilized in material science for the development of new materials with unique properties, such as polymers and composites, due to its reactive functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 10562-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,6 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10562-68:
(7*1)+(6*0)+(5*5)+(4*6)+(3*2)+(2*6)+(1*8)=82
82 % 10 = 2
So 10562-68-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O/c1-6-11(12,7-9(2)3)8-10(4)5/h1,9-10,12H,7-8H2,2-5H3
10562-68-2Relevant academic research and scientific papers
Pd(II)-catalyzed highly regio-and stereoselective assembly of C-C double bonds: An efficient method for the synthesis of 2,4-dihalo-1,3,5-trienes from alkynols
Jiang, Huanfeng,Gao, Yang,Wu, Wanqing,Huang, Yubing
supporting information, p. 238 - 241 (2013/03/13)
A highly efficient method for the synthesis of 2,4-dihalo-1,3,5-trienes from alkynols was developed. This chemistry allows access to multiple conjugated double bonds in a single step with high stereoselectivity.
