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940274-21-5

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940274-21-5 Usage

General Description

Allyl 2-O-benzoyl-3-O-benzyl-a-L-rhamnopyranoside is a chemical compound composed of allyl, benzoyl, benzyl, and a-L-rhamnopyranoside groups. It is a glycoside, which means it contains a sugar molecule attached to a non-sugar moiety. Allyl 2-O-benzoyl-3-O-benzyl-a-L-rhamnopyranoside is commonly used in organic synthesis and as a building block for the production of other chemicals. It has potential applications in pharmaceuticals, as well as in the flavor and fragrance industry due to its aromatic properties. Additionally, the benzoyl and benzyl groups allow for modifications to be made to the molecule, making it useful for further chemical reactions and derivatization. Overall, Allyl 2-O-benzoyl-3-O-benzyl-a-L-rhamnopyranoside is a versatile compound with broad potential for various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 940274-21-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,0,2,7 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 940274-21:
(8*9)+(7*4)+(6*0)+(5*2)+(4*7)+(3*4)+(2*2)+(1*1)=155
155 % 10 = 5
So 940274-21-5 is a valid CAS Registry Number.

940274-21-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Allyl 2-O-benzoyl-3-O-benzyl-a-L-rhamnopyranoside

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

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More Details:940274-21-5 SDS

940274-21-5Downstream Products

940274-21-5Relevant articles and documents

Silver(I) oxide-mediated regioselective 2-monoacylation in 3-O-benzyl-α-l-rhamnopyranosides and application in synthesis of a protected tetrasaccharide fragment of potent cytotoxic saponins gleditsiosides C and D

Yang, Qian,Lei, Ming,Yin, Qin-Jian,Yang, Jin-Song

, p. 1175 - 1181 (2008/02/02)

The axial 2-hydroxyl group of methyl and allyl 3-O-benzyl-α-l-rhamnopyranosides was selectively acylated in 56-78% yields by reaction with 1.1 equiv of acyl chloride in the presence of 1.5 equiv of silver(I) oxide. Use of the method permitted a convenient

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