5355-63-5 Usage
Description
3-HYDROXY-4-PHENYLBUTAN-2-ONE, also known as a phenylbutanone derivative, is an organic compound that is reportedly present in honey, sherry, and wine. It is characterized by its pleasant, mild, warm, and creamy sweet fragrance, making it a potential candidate for various applications in different industries.
Uses
Used in Flavor and Fragrance Industry:
3-HYDROXY-4-PHENYLBUTAN-2-ONE is used as a flavoring agent for its pleasant and creamy sweet fragrance, enhancing the taste and aroma of various food and beverage products.
Used in Perfumery:
3-HYDROXY-4-PHENYLBUTAN-2-ONE is used as a fixative in the perfumery industry, where its warm and mild fragrance helps to stabilize and prolong the scent of perfumes and colognes.
Used in Pharmaceutical Industry:
3-HYDROXY-4-PHENYLBUTAN-2-ONE can be used as an intermediate in the synthesis of various pharmaceutical compounds, potentially contributing to the development of new drugs with diverse therapeutic applications.
Used in Cosmetics:
3-HYDROXY-4-PHENYLBUTAN-2-ONE may be utilized in the cosmetics industry for its fragrance, where it can be incorporated into various products such as lotions, creams, and shampoos to provide a pleasant and appealing scent.
Used in Research and Development:
3-HYDROXY-4-PHENYLBUTAN-2-ONE can be employed as a research compound for studying its chemical properties, potential applications, and interactions with other molecules, which may lead to the discovery of new uses and benefits in various industries.
Preparation
Reported prepared by a Japanese Patent (details not available)
Check Digit Verification of cas no
The CAS Registry Mumber 5355-63-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5355-63:
(6*5)+(5*3)+(4*5)+(3*5)+(2*6)+(1*3)=95
95 % 10 = 5
So 5355-63-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O2/c1-8(11)10(12)7-9-5-3-2-4-6-9/h2-6,10,12H,7H2,1H3
5355-63-5Relevant articles and documents
Cu-catalyzed synthesis of tetrasubstituted 2,3-allenols through decarboxylative silylation of alkyne-substituted cyclic carbonates
Guo, Kun,Kleij, Arjan W.
, p. 3942 - 3945 (2020/06/08)
An efficient and mild Cu-catalyzed protocol has been developed for the decarboxylative silylation of alkyne-functionalized cyclic carbonate substrates affording 2,3-allenols featuring four different substituents. This practical methodology gives access to a wide scope of tetrasubstituted functionalized allenes in excellent yields.
I2- or NBS-catalyzed highly efficient α-hydroxylation of ketones with dimethyl sulfoxide
Liang, Yu-Feng,Wu, Kai,Song, Song,Li, Xinyao,Huang, Xiaoqiang,Jiao, Ning
supporting information, p. 876 - 879 (2015/04/14)
An efficient method for the direct preparation of high synthetic valuable α-hydroxycarbonyls is described. The simple and readily available I2 or NBS was used as catalyst. DMSO acts as the oxidant, oxygen source, and solvent. A diverse range of tertiary Csp3-H bonds as well as more challenging secondary Csp3-H bonds could be hydroxylated in this transformation. The reaction is mild, less toxic and easy to perform.
Branched-chain keto acid decarboxylase from Lactococcus lactis (KdcA), a valuable thiamine diphosphate-dependent enzyme for asymmetric C - C bond formation
Gocke, Doerte,Nguyen, Cong Luan,Pohl, Martina,Stillger, Thomas,Walter, Lydia,Mueller, Michael
, p. 1425 - 1435 (2008/04/03)
The thiamine diphosphate-dependent, branched-chain 2-keto acid decarboxylase from Lactococcus lactis sup. cremoris Bl157 (KdcA) is a new valuable enzyme for the synthesis of chiral 2-hydroxy ketones. The gene was cloned and the enzyme was expressed as an
