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124378-00-3

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124378-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124378-00-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,3,7 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 124378-00:
(8*1)+(7*2)+(6*4)+(5*3)+(4*7)+(3*8)+(2*0)+(1*0)=113
113 % 10 = 3
So 124378-00-3 is a valid CAS Registry Number.

124378-00-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3R,4S,5S,6R)-2-(2-hydroxyethylamino)-6-(hydroxymethyl)oxane-3,4,5-triol

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:124378-00-3 SDS

124378-00-3Downstream Products

124378-00-3Relevant articles and documents

Synthesis and evaluation of N-alkyl-β-d-glucosylamines on the growth of two wood fungi, Coriolus versicolor and Poria placenta

Muhizi, Theoneste,Coma, Veronique,Grelier, Stephane

, p. 2369 - 2375 (2008)

Various glucosylamines were synthesized from glucose and different alkyl amine compounds. These amino compounds are β-d-glucopyranosylamine (GPA), N-ethyl-β-d-glucopyranosylamine (EtGPA), N-butyl-β-d-glucopyranosylamine (BuGPA), N-hexyl-β-d-glucopyranosyl

Cyclic structure of the β(γ)-hydroxy-(mercapto)alkylimines of aldoses

Alekseev,Zelenin

, p. 919 - 922 (2007/10/03)

In solutions in DMSO-d6, the products from the condensation of ethanolamine and 1,2- and 1,3-aminopropanols with aldoses are mixtures of the α- and β-pyranose forms, whereas the β-mercaptoethylimines of aldoses have the 1,3-thiazolidine structure. Glucose β-mercaptoethylimine is characterized by ring - chain tautomerism involving the α-pyranose and diastereomeric 1,3-thiazolidine tautomers. 1999 Kluwer Academic/Plenum Publishers.

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