18525-42-3 Usage
Description
(4-tert-butylcyclohexyl)(phenyl)methanone, also known as TBCM, is a chemical compound belonging to the ketone class with a molecular formula C21H28O. It is a white crystalline solid characterized by its sweet floral odor and is commonly utilized as a fragrance ingredient in the perfumery and personal care industries. TBCM is appreciated for its stability and relatively low volatility, which makes it suitable for a wide range of cosmetic applications. In addition to its use in the fragrance sector, TBCM also serves as an intermediate in the synthesis of other organic compounds. However, due to its potential hazards, it is crucial to handle this chemical with care and adhere to safety guidelines.
Uses
Used in Fragrance Industry:
TBCM is used as a fragrance ingredient for its sweet floral scent, adding a pleasant aroma to perfumes and personal care products. Its stability and low volatility contribute to its widespread use in this application.
Used in Cosmetics Industry:
In the cosmetics industry, TBCM is employed as an additive to enhance the fragrance of various products, such as lotions, creams, and shampoos. Its compatibility with a range of cosmetic formulations makes it a valuable component in the development of scented products.
Used as an Intermediate in Organic Synthesis:
TBCM is also utilized as an intermediate in the synthesis of other organic compounds, showcasing its versatility in the chemical industry. Its role in creating a variety of products highlights its importance in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 18525-42-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,2 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18525-42:
(7*1)+(6*8)+(5*5)+(4*2)+(3*5)+(2*4)+(1*2)=113
113 % 10 = 3
So 18525-42-3 is a valid CAS Registry Number.
18525-42-3Relevant articles and documents
Stereoselective Protonation of Carbanions, 1. - Diastereoselective Protonation of C-H-Activated Cyclohexane Derivatives
Gerlach, Uwe,Haubenreich, Thomas,Huenig, Siegfried,Keita, Yango
, p. 1205 - 1216 (2007/10/02)
The diastereoselectivity of the kinetically controlled protonation of carbanions derived from 4-tert-butyl-1-X-cyclohexanes (1: X = CN, 2: X = CO2Me, 2-Si: X = C(OMe)OSiMe3, 3: X = COPh, 4: X = SO2Ph) is systematically investigated.By variation of (a) the
