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1,2-Ethanediol, 1-(1,3-dithian-2-yl)-, 2-(4-methylbenzenesulfonate), (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86040-14-4

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86040-14-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86040-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,0,4 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86040-14:
(7*8)+(6*6)+(5*0)+(4*4)+(3*0)+(2*1)+(1*4)=114
114 % 10 = 4
So 86040-14-4 is a valid CAS Registry Number.

86040-14-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-O-Tosyl-D-glycero-triose-trimethylendithioacetal

1.2 Other means of identification

Product number -
Other names Toluene-4-sulfonic acid (R)-2-[1,3]dithian-2-yl-2-hydroxy-ethyl ester

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:86040-14-4 SDS

86040-14-4Downstream Products

86040-14-4Relevant academic research and scientific papers

Chiral Buildung Units from Carbohydrates, IX. - Synthesis of Enantiomeric 2,8-Dimethyl-1,7-dioxaspiroundecan-4-ols, Components from the Pheromone Bouquet of Andrena wilkella

Redlich, Hartmut,Schneider, Bernd

, p. 412 - 424 (2007/10/02)

The enantiomeric spiro acetals 29 and 35 are synthesized via the open-chained compounds 27 and 33 which are obtained by connecting the open-chained, D- or L-threo configurated, blocked trideoxytrimethylene dithioacetals IV with 1-iodo-4-(tetrahydropyranoloxy)pentane (1).One of the two enantiomers 29 or 35 represents a component from the pheromone bouquet of Andrena wilkella.The synthesis of racemic 1 is described as well as the synthesis of 1 in optically pure form in two different, independent ways, starting from D-glyceraldehyde and D-glucose.

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