705-58-8 Usage
Description
3-methyl-1-phenylbutan-2-ol, also known as isovalerol phenyl ethyl alcohol, is a colorless liquid chemical compound with a molecular formula of C12H18O. It possesses a sweet, floral, and somewhat fruity odor, making it a versatile ingredient in various industries.
Uses
Used in Fragrance Industry:
3-methyl-1-phenylbutan-2-ol is used as a fragrance ingredient for its sweet, floral, and fruity scent. It is incorporated into the production of perfumes, soaps, and other cosmetic products to enhance their aroma and appeal to consumers.
Used in Food Industry:
In the food industry, 3-methyl-1-phenylbutan-2-ol is used as a flavoring agent to impart a pleasant taste and aroma to various food products. Its unique scent profile adds depth and complexity to the flavor profiles of different food items.
Used in Pharmaceutical Industry:
3-methyl-1-phenylbutan-2-ol has been investigated for its potential use in the pharmaceutical industry due to its antimicrobial and antioxidant properties. Its ability to combat microbes and neutralize harmful free radicals makes it a promising candidate for the development of new drugs and treatments.
Used in Cosmetic Products:
3-methyl-1-phenylbutan-2-ol is used in cosmetic products as it is considered relatively safe when used in appropriate concentrations. Its sweet, floral, and fruity odor adds a pleasant scent to these products, enhancing their overall sensory experience for consumers.
However, it is important to note that 3-methyl-1-phenylbutan-2-ol may cause skin irritation, and therefore, it should be handled with care to avoid adverse effects on the skin.
Check Digit Verification of cas no
The CAS Registry Mumber 705-58-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 705-58:
(5*7)+(4*0)+(3*5)+(2*5)+(1*8)=68
68 % 10 = 8
So 705-58-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O/c1-9(2)11(12)8-10-6-4-3-5-7-10/h3-7,9,11-12H,8H2,1-2H3
705-58-8Relevant articles and documents
INHIBITORS OF NOROVIRUS AND CORONAVIRUS REPLICATION
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Paragraph 002112-002114, (2021/10/15)
Compounds of Formula (I) and methods of inhibiting the replication of viruses in a biological sample or patient, of reducing the amount of viruses in a biological sample or patient, and of treating a virus infection in a patient, comprising administering to said biological sample or patient an effective amount of a compound represented by Formula (I), a compound of Table A or B or a pharmaceutically acceptable salt thereof.
Photocatalytic carbanion generation-benzylation of aliphatic aldehydes to secondary alcohols
Donabauer, Karsten,Maity, Mitasree,Berger, Anna Lucia,Huff, Gregory S.,Crespi, Stefano,K?nig, Burkhard
, p. 5162 - 5166 (2019/06/05)
We present a redox-neutral method for the photocatalytic generation of carbanions. Benzylic carboxylates are photooxidized by single electron transfer; immediate CO2 extrusion and reduction of the in situ formed radical yields a carbanion capable of reacting with aliphatic aldehydes as electrophiles giving the Grignard analogous reaction product.
A General, Practical Triethylborane-Catalyzed Reduction of Carbonyl Functions to Alcohols
Peng, Dongjie,Zhang, Mintao,Huang, Zheng
supporting information, p. 14737 - 14741 (2015/10/19)
A combination of the abundant and low-cost triethylborane and sodium alkoxide generates a highly efficient catalyst for reduction of esters, as well as ketones and aldehydes, to alcohols using an inexpensive hydrosilane under mild conditions. The catalyst system exhibits excellent chemoselectivity and a high level of functional group tolerance. Mechanistic studies revealed a resting state of sodium triethylalkoxylborate that is the product of the reaction of BEt3 with sodium alkoxide. This borate species reacts with hydrosilane to form NaBEt3H, which rapidly reduces esters.
