34131-98-1 Usage
Description
DECATONE, also known as 6-Isopropyl-2-decahydronaphthalenol, is a chemical compound derived from the synthesis process. It is characterized by its unique molecular structure and properties, making it a valuable component in various applications.
Source:
DECATONE is synthesized through a series of chemical reactions, resulting in a compound with specific properties that are useful in different industries.
Production Methods:
The production of DECATONE involves a series of chemical reactions and processes that transform raw materials into the desired compound.
Uses
Used in Perfumery Industry:
DECATONE is used as a fragrance raw material for its distinct and appealing scent. It contributes to the creation of various perfumes and fragrances, enhancing their overall aroma and appeal to consumers.
Check Digit Verification of cas no
The CAS Registry Mumber 34131-98-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,3 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 34131-98:
(7*3)+(6*4)+(5*1)+(4*3)+(3*1)+(2*9)+(1*8)=91
91 % 10 = 1
So 34131-98-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H22O/c1-9(2)10-3-4-12-8-13(14)6-5-11(12)7-10/h9-12H,3-8H2,1-2H3
34131-98-1Relevant articles and documents
Enolization of 2-Decalones
Huffman, John W.,Balke, William H.
, p. 3828 - 3831 (2007/10/02)
It is well-known that under thermodynamic conditions 5α-3-keto steroids such as 3-cholestanone enolize predominantly toward C-2, while the 5β-isomers enolize toward C-4.It has been tacitly assumed that 2-decalones, bicyclic analogues of the steroids, show similar selectivity.In a systematic investigation of the direction of enolization of 2-decalones, 11 bicyclic ketones plus two representative steroids have been converted to the corresponding trimethylsilyl enol ethers under thermodynamic conditions.The classical generalizations have been found to be valid for trans-2-decalones and steroidally locked cis-2-decalones with an angular methyl group.Nonsteroidally locked cis-2-decalones with an angular methyl enolize in a direction opposite to that predicted.Without an angular methyl, all three types of 2-decalones enolize in the predicted manner, but with attenuated regioselectivity.Molecular-mechanics calculations have been carried out for the olefins corresponding to decalone enols.With the exception of the nonsteroidal cis compounds with an angular methyl, the calculations agree well with the experimental data.
