73573-57-6 Usage
Description
Benzyl 2,3-dihydroxypropanoate is a chemical compound that features a benzyl group attached to a 2,3-dihydroxypropanoate group. It is recognized for its distinctive sweet, floral, and fruity aroma, which contributes to its widespread use in the fragrance industry.
Uses
Used in Fragrance Industry:
Benzyl 2,3-dihydroxypropanoate serves as a key fragrance ingredient due to its appealing scent profile. It is utilized for imparting a sweet, floral, and fruity aroma to a variety of consumer products, enhancing their sensory appeal and consumer experience.
Used in Cosmetics and Personal Care Products:
In the cosmetics and personal care sector, benzyl 2,3-dihydroxypropanoate is employed as a fragrance component. Its incorporation into these products allows for the creation of pleasant and attractive scents, which can improve the overall user experience and product acceptance.
Used in Perfumes:
Benzyl 2,3-dihydroxypropanoate is also a popular choice in the formulation of perfumes. Its unique aroma adds depth and complexity to perfume blends, contributing to the creation of distinctive and memorable fragrances.
Check Digit Verification of cas no
The CAS Registry Mumber 73573-57-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,5,7 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73573-57:
(7*7)+(6*3)+(5*5)+(4*7)+(3*3)+(2*5)+(1*7)=146
146 % 10 = 6
So 73573-57-6 is a valid CAS Registry Number.
73573-57-6Relevant articles and documents
Dihydroxylation of Olefins with Potassium Permanganate Catalyzed by Imidazolium Salt
Khan, Imran,Luo, Zhi-Bin,Valeru, Anil,Xu, Yin,Liu, Bin,Sangepu, Bhavanarushi,Xie, Ji-Min
, p. 1815 - 1819 (2018/02/19)
The development of an efficient and cost-effective cis -dihydroxylation reaction of acrylate derivatives was achieved. The reaction proceeded in acetone with an imidazolium salt as catalyst to furnish the dihydroxylation of olefins at 0-5 °C using KMnO 4 as the oxidant. This efficient and non-aqueous protocol was highly suitable for the large-scale preparation of cis -dihydroxylated compounds from the corresponding acrylate derivatives in high yields without overoxidation.
INHIBITORS OF ACTIVIN RECEPTOR-LIKE KINASE
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Page/Page column 265; 266, (2017/11/10)
Described herein are compounds that inhibit ALK2 and its mutants, pharmaceutical compositions including such compounds, and methods of using such compounds and compositions.
MASKED CARBOXYLATE NEOPENTYL SULFONYL ESTER CYCLIZATION RELEASE PRODRUGS OF ACAMPROSATE, COMPOSITIONS THEREOF, AND METHODS OF USE
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Page/Page column 50, (2009/04/24)
Masked carboxylate neopentyl sulfonyl ester prodrugs of acamprosate, pharmaceutical compositions comprising such prodrugs, and methods of using such prodrugs and compositions thereof for treating diseases are disclosed. In particular, acamprosate prodrugs