23832-18-0 Usage
Description
PINANYL MERCAPTAN, also known as 2-, 3-, or 10-Mercaptopinane, is a chemical compound with a distinctive sulfurous, tropical fruit odor and a grapefruit taste. It is composed of approximately 54% 10-isomer, 31% 2-isomer, and 10% 3-isomer. PINANYL MERCAPTAN is characterized by its sulfurous, metallic, tropical, woody, fresh, green, and cooling taste profile.
Uses
Used in Flavor and Fragrance Industry:
PINANYL MERCAPTAN is used as a flavoring agent for its unique grapefruit taste, adding a tropical and fresh note to various food and beverage products.
PINANYL MERCAPTAN is also used as a fragrance ingredient for its sulfurous, metallic, tropical, woody, fresh, green, and cooling scent, enhancing the aroma of perfumes, cosmetics, and other scented products.
Used in Chemical Industry:
PINANYL MERCAPTAN serves as a building block or intermediate in the synthesis of various organic compounds, taking advantage of its distinct chemical properties and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 23832-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,8,3 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 23832-18:
(7*2)+(6*3)+(5*8)+(4*3)+(3*2)+(2*1)+(1*8)=100
100 % 10 = 0
So 23832-18-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H18S/c1-9(2)7-4-5-10(3,11)8(9)6-7/h7-8,11H,4-6H2,1-3H3
23832-18-0Relevant articles and documents
ELECTROPHILIC THIYLATION OF BICYCLIC MONOTERPENES BY HYDROGEN SULFIDE AND 1-BUTANETHIOL
Tolstikov, G. A.,Kanzafarov, F. Ya.,Dzhemilev, U. M.,Kantyukova, R. G.,Zelenova, L. M.
, p. 1799 - 1804 (2007/10/02)
The thiylation of α,β-pinenes and camphene by hydrogen sulfide and 1-butanethiol, catalyzed by aluminum halides and alkylaluminum halides, was investigated.The regioselectivity and stereoselectivity of the reaction depend on the acidity of the catalyst.The thiylation of pinenes by hydrogen sulfide in the presence of alkylaluminum halides leads to the preferential formation of trans-pinane-2-thiol, and the catalyst with the higher acidity (aluminum bromide) promotes the menthene isomerization of the pinenes.
