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115678-08-5

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115678-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115678-08-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,6,7 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 115678-08:
(8*1)+(7*1)+(6*5)+(5*6)+(4*7)+(3*8)+(2*0)+(1*8)=135
135 % 10 = 5
So 115678-08-5 is a valid CAS Registry Number.

115678-08-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 1-thio-α-L-rhamnopyranoside

1.2 Other means of identification

Product number -
Other names (2S,3R,4R,5R,6S)-2-Methyl-6-methylsulfanyl-tetrahydro-pyran-3,4,5-triol

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:115678-08-5 SDS

115678-08-5Relevant articles and documents

Synthesis of Oligosaccharides Corresponding to the Common Polysaccharide Antigen of Group B Streptococci

Pozsgay, Vince,Jennings, Harold J.

, p. 4042 - 4052 (2007/10/02)

To facilitate mapping of the immunodominant region of the common polysaccharide antigen of group B streptococci, tetrasaccharide 1-O--α-rhamnopyranosyl>-D-glucitol (2) was synthesized in a stepwise fasion

A Through-process for the Preparation of Methyl Per-O-acetyl 1-Thio-glycosides from Aldoses

Koto, Shinkiti,Yoshida, Toyosaku,Takenaka, Kazuhiro,Zen, Shonosuke

, p. 3667 - 3668 (2007/10/02)

D-Glucose, D-galactose, D-mannose, D-xylose, L-arabinose, L-fucose, L-rhamnose, maltose, cellobiose, lactose, D-glucosamine, D-galactosamine, and D-mannosamine were converted into the corresponding methyl per-O-acetyl 1-thioglycopyranosides by way of a three-step (acetobromination, methylthioation, and acetylation) through-process in a single vessel.

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