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24332-96-5

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24332-96-5 Usage

General Description

2,3,4-Tri-O-acetyl-α-L-fucopyranosyl chloride is a chemical compound that is derived from fucose, a type of sugar. It is an acetylated derivative of fucose and is used in various chemical and biological applications. 2,3,4-Tri-O-acetyl-α-L-fucopyranosyl chloride is a chlorinated form of fucopyranosyl chloride and is commonly used in the synthesis of complex carbohydrates and glycoproteins. It is also used as a building block for the modification of biomolecules and as a reagent in organic chemistry reactions. 2,3,4-Tri-O-acetyl-α-L-fucopyranosyl chloride is a versatile compound that has applications in both research and industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 24332-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,3 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24332-96:
(7*2)+(6*4)+(5*3)+(4*3)+(3*2)+(2*9)+(1*6)=95
95 % 10 = 5
So 24332-96-5 is a valid CAS Registry Number.

24332-96-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4-Tri-O-acetyl-α-L-fucopyranosyl chloride

1.2 Other means of identification

Product number -
Other names ACETOCHLORO-ALPHA-L-FUCOSE

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:24332-96-5 SDS

24332-96-5Relevant articles and documents

Regioselective activation of glycosyl acceptors by a diarylborinic acid-derived catalyst

Gouliaras, Christina,Lee, Doris,Chan, Lina,Taylor, Mark S.

supporting information; experimental part, p. 13926 - 13929 (2011/10/31)

A derivative of diphenylborinic acid promotes catalytic, regioselective Koenigs-Knorr glycosylations of carbohydrate derivatives bearing multiple secondary hydroxyl groups. Robust levels of selectivity for the equatorial OH group of cis-1,2-diol motifs ar

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