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73573-57-6

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73573-57-6 Usage

General Description

Benzyl 2,3-dihydroxypropanoate is a chemical compound that consists of a benzyl group and a 2,3-dihydroxypropanoate group. It is commonly used as a fragrance ingredient in cosmetics, perfumes, and personal care products. This chemical is known for its sweet, floral, and fruity aroma, making it a popular choice for adding pleasant scents to various consumer products. However, it is important to note that benzyl 2,3-dihydroxypropanoate may cause skin irritation and allergic reactions in some individuals, and should be used with caution in formulations and applications.

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.

73573-57-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 2,3-dihydroxypropanoate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:73573-57-6 SDS

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

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