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3-Cyclohexene-1-carboxylic acid, (3R)-tetrahydro-4,4-dimethyl-2-oxo-3-furanyl ester, (1S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102096-64-0

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102096-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102096-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,0,9 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 102096-64:
(8*1)+(7*0)+(6*2)+(5*0)+(4*9)+(3*6)+(2*6)+(1*4)=90
90 % 10 = 0
So 102096-64-0 is a valid CAS Registry Number.

102096-64-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Cyclohexene-1-carboxylic acid (R)-pentalactone ester

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:102096-64-0 SDS

102096-64-0Relevant academic research and scientific papers

An asymmetric synthesis of (+)-phyllanthocin

Trost,Kondo

, p. 1613 - 1616 (2007/10/02)

An enantiocontrolled synthesis of (+)-phyllanthocin from methyl R-3-hydroxylisobutyrate and the acrylic ester of D-pantolactone is accomplished in 20 steps in 5% overall yield.

DIASTEREOFACE-DISCRIMINATIVE METAL COORDINATION IN ASYMMETRIC SYNTHESIS: D-PANTOLACETONE AS PRACTICAL CHIRAL AUXILIARY FOR LEWIS ACID CATALYZED DIELS-ALDER REACTIONS

Poll, Thomas,Sobczak, Andrzej,Hartmann, Horst,Helmchen, Gunter

, p. 3095 - 3098 (2007/10/02)

TiCl4-catalyzed Diels-Alder additions of the acrylate of commercial D-pantoloacetone to cyclopentadiene, isoprene and butadiene proceed with very high diastereofacial selectivity.Practical and mechanistic aspects of these reactions are discussed.

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