2035-93-0 Usage
Description
4-methyl-4-phenylpentan-2-ol, also known as Dimethyl Phenylbutanol, is an organic compound with the molecular formula C15H22O. It is a colorless to pale yellow liquid with a mild, sweet, and floral odor. 4-methyl-4-phenylpentan-2-ol is characterized by its unique molecular structure, which includes a methyl group, a phenyl group, and a pentan-2-ol group, making it a versatile compound with various applications across different industries.
Uses
Used in Cosmetics Industry:
4-methyl-4-phenylpentan-2-ol is used as an antimicrobial agent for cosmetics to prevent the growth of harmful microorganisms and ensure the safety and longevity of cosmetic products. Its antimicrobial properties help maintain the integrity of the products, reducing the risk of contamination and spoilage.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-methyl-4-phenylpentan-2-ol is used as an antimicrobial agent in the production of drugs. It helps to preserve the drugs and prevent the growth of bacteria, fungi, and other microorganisms that could compromise the drug's efficacy and safety.
Used in Preservatives Industry:
4-methyl-4-phenylpentan-2-ol is also used as a preservative in various industries, including the food and beverage industry. Its antimicrobial properties help to extend the shelf life of products by inhibiting the growth of spoilage-causing microorganisms, ensuring the freshness and quality of the products.
Check Digit Verification of cas no
The CAS Registry Mumber 2035-93-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,3 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2035-93:
(6*2)+(5*0)+(4*3)+(3*5)+(2*9)+(1*3)=60
60 % 10 = 0
So 2035-93-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O/c1-10(13)9-12(2,3)11-7-5-4-6-8-11/h4-8,10,13H,9H2,1-3H3
2035-93-0Relevant articles and documents
Stereoselective radical Aryl migration reactions from sulfur to carbon
Bossart, Martin,Faessler, Roger,Schoenberger, Jan,Studer, Armido
, p. 2742 - 2757 (2007/10/03)
Stereoselective aryl migration reactions from sulfur in sulfonates and sulfonamides to C-centered radicals are reported. The 1,5-aryl migration from sulfur to differently substituted C-centered radicals could be performed with high yields and selectivities. Functionalized aryl groups could also be transferred by this new method. A model to explain the stereochemical outcome of the reaction is presented and some mechanistic aspects of this reaction are discussed. Aryl migration reactions from sulfur in sulfinates to carbon radicals were less efficient, and the corresponding migrations in aryl sulfoxides were not observed at all. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.
