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23661-35-0

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23661-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23661-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,6,6 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23661-35:
(7*2)+(6*3)+(5*6)+(4*6)+(3*1)+(2*3)+(1*5)=100
100 % 10 = 0
So 23661-35-0 is a valid CAS Registry Number.

23661-35-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 6-O-p-toluenesulfonyl-β-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names METHYL 6-O-TOSYL-BETA-D-GLUCOPYRANOSIDE

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:23661-35-0 SDS

23661-35-0Relevant articles and documents

New class of quaternary ammonium salts, derivatives of methyl D-glucopyranosides

Pellowska-Januszek, Lucyna,Dmochowska, Barbara,Skorupa, Eugenia,Chojnacki, Jaroslaw,Wojnowski, Wieslaw,Wisniewski, Andrzej

, p. 1537 - 1544 (2004)

Reactions of two aromatic and two aliphatic amines with methyl 6-O-p-toluenesulfonyl-α-D-glucopyranoside or methyl 6-O-p-toluenesulfonyl- β-D-glucopyranoside were performed on a micro-scale. The synthesis and preparative isolation methods have been develo

Cluster glycosides and heteroglycoclusters presented in alternative arrangements

Figueredo, Andreza S.,Zamoner, Luis O.B.,Rejzek, Martin,Field, Robert A.,Carvalho, Ivone

supporting information, p. 4405 - 4409 (2018/11/10)

Multivalent carbohydrates, or glycoclusters, are useful tools to study glycan-lectin and glycan-enzyme recognition processes and have wide potential therapeutic applicability. Herein, we report the synthesis of novel glycoclusters presenting glucopyranose

Quantifying the electronic effects of carbohydrate hydroxy groups by using aminosugar models

Pedersen, Christian M.,Olsen, Jacob,Brka, Azra B.,Bols, Mikael

scheme or table, p. 7080 - 7086 (2011/07/08)

Methyl amino-deoxy-glycosides with α- and β-gluco, α-galacto, or α-manno stereochemistry with the amino functionality in each of the four possible non-anomeric positions have been synthesized and their pKa values determined by titration. These

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