7145-23-5 Usage
Uses
Used in Organic Synthesis:
2,3-DIMETHYL-3-HEXENE is used as a starting material for the synthesis of various other organic compounds, contributing to the creation of a wide range of chemical products.
Used in Fragrance and Flavor Production:
2,3-DIMETHYL-3-HEXENE is used as a component in the production of fragrances and flavors, adding unique scents and tastes to various consumer products.
Used in Specialty Chemicals:
2,3-DIMETHYL-3-HEXENE is utilized in the production of specialty chemicals, which are often used in specific applications due to their unique properties.
Used as a Solvent in Industrial Processes:
2,3-DIMETHYL-3-HEXENE serves as a solvent in some industrial processes, aiding in the dissolution of other substances for various applications.
Safety Note:
It is important to handle 2,3-DIMETHYL-3-HEXENE with caution, as it may be harmful if inhaled, absorbed through the skin, or ingested. Proper safety measures should be taken during its use to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 7145-23-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7145-23:
(6*7)+(5*1)+(4*4)+(3*5)+(2*2)+(1*3)=85
85 % 10 = 5
So 7145-23-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H16/c1-5-6-8(4)7(2)3/h6-7H,5H2,1-4H3/b8-6+
7145-23-5Relevant academic research and scientific papers
Scope and Regiochemical Control of the Allylpotassium Reaction in the Synthesis of Sterols with Unsaturated Side Chains
Giner, Jose-Luis,Margot, Christian,Djerassi, Carl
, p. 2117 - 2125 (2007/10/02)
Allylpotassium derivatives were prepared from a variety of olefins by using Schlosser's base (BuLi/KOt-Bu).Reaction with (20S)-20-(iodomethyl)pregnane i-methyl ether (1) followed by deprotection gave in high yields a wide variety of Δ24 and Δ24(28) sterols, including the naturally occuring desmosterol (37), fucosterol (33), 24(E)-propylidenecholesterol (35), 24-methylenecholesterol (3), dehydroaplysterol (10), 25-methyl-24-methylenecholesterol (11), mutasterol (12), and 25-methylxestosterol (13).Control of the regiochemistry of unsymmetrical allylmetals was achieved through the addition of Li2CuCl3.Rules concerning the high regioselectivities and stereoselectivities are discussed.
