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29514-09-8

29514-09-8

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29514-09-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29514-09-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,1 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 29514-09:
(7*2)+(6*9)+(5*5)+(4*1)+(3*4)+(2*0)+(1*9)=118
118 % 10 = 8
So 29514-09-8 is a valid CAS Registry Number.

29514-09-8SDS

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 1,6-anhydro-3-deoxy-β-D-arabino-hexopyranose

1.2 Other means of identification

Product number -
Other names β-D-arabino-1,6-Anhydro-3-desoxy-hexopyranose

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:29514-09-8 SDS

29514-09-8Relevant articles and documents

Preparation of the diastereomerically pure 2S-hydroxy derivative of dihydrolevoglucosenone (cyrene)

Sharipov, Bulat T.,Davydova, Anna N.,Faizullina, Liliya Kh.,Valeev, Farid A.

, p. 200 - 202 (2019/04/25)

Diastereomerically pure levoglucosenone alcohol, synthesized from levoglucosenone, upon hydrogenation on Raney Ni or Pd/BaSO4 undergoes epimerization at C2 atom caused by formation of cyrene by-product and its subsequent non-specific

Manipulating the enone moiety of levoglucosenone: 1,3-Transposition reactions including ones leading to isolevoglucosenone

Ma, Xinghua,Liu, Xin,Yates, Patrick,Raverty, Warwick,Banwell, Martin G.,Ma, Chenxi,Willis, Anthony C.,Carr, Paul D.

, p. 5000 - 5011 (2018/06/20)

The manipulation of the enone moiety associated with the biomass-derived, homochiral and now abundant compound levoglucosenone (1) is described. While the trichloroacetimidates derived from the allylic alcohols 3 and 4 failed to engage in Overman-type rea

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