42161-41-1 Usage
Description
3-Methyl-5-pentyl-2-cyclohexen-1-one, also known as 3-Methyl-5-pentylcyclohex-2-en-1-one, is a cyclohexenone derivative with the molecular formula C12H20O. It features a cyclohexene ring with a methyl group at position 3 and a pentyl group at position 5, contributing to its unique chemical structure.
Used in Fragrance Industry:
3-Methyl-5-pentyl-2-cyclohexen-1-one is used as a fragrance ingredient for its fruity, floral, and woody odor, enhancing the scent profiles of various consumer products.
Used in Flavoring Industry:
In the flavoring industry, 3-Methyl-5-pentyl-2-cyclohexen-1-one is used as a flavoring agent to impart its characteristic taste to food and beverages.
Used in Pharmaceutical Industry:
3-Methyl-5-pentyl-2-cyclohexen-1-one is used as a starting material in the synthesis of pharmaceutical compounds, leveraging its chemical properties for the development of new drugs.
Used in Agricultural Industry:
In agriculture, 3-Methyl-5-pentyl-2-cyclohexen-1-one has potential applications due to its biological activities, which can be harnessed for pest control or other agricultural purposes.
Used in Chemical Synthesis:
3-Methyl-5-pentyl-2-cyclohexen-1-one is used as an intermediate in the synthesis of other organic compounds, serving as a building block for creating a variety of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 42161-41-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,1,6 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 42161-41:
(7*4)+(6*2)+(5*1)+(4*6)+(3*1)+(2*4)+(1*1)=81
81 % 10 = 1
So 42161-41-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O/c1-3-4-5-6-11-7-10(2)8-12(13)9-11/h8,11H,3-7,9H2,1-2H3
42161-41-1Relevant articles and documents
Enantioselective aldol cyclodehydrations catalyzed by antibody 38C2.
List,Lerner,Barbas 3rd.
, p. 59 - 61 (2008/02/11)
[formula: see text] Aldolase antibody 38C2 catalyzes the enantioselective aldol cyclodehydration of 4-substituted-2,6-heptanediones (3) to give enantiomerically enriched 5-substituted-3-methyl-2-cyclohexen-1-ones (4). Yields, enantioselectivities, and pro