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1H-Cyclopentacyclododecene-4,9-dione,1,3a,10-tris(acetyloxy)-11,13-bis(benzoyloxy)-2,3,3a,5,8,10,11,12,13,13a-decahydro-2-hydroxy-2,5,8,8-tetramethyl-12-methylene-,(1R,2R,3aR,5S,6E,10R,11S,13R,13aS)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100198-26-3

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100198-26-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100198-26-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,9 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 100198-26:
(8*1)+(7*0)+(6*0)+(5*1)+(4*9)+(3*8)+(2*2)+(1*6)=83
83 % 10 = 3
So 100198-26-3 is a valid CAS Registry Number.

100198-26-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name esulone B

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:100198-26-3 SDS

100198-26-3Downstream Products

100198-26-3Relevant academic research and scientific papers

The Absolute Stereochemical Characterization of Two New Jatrophane Diterpenes from Euphorbia esula

Manners, Gary D.,Wong, Rosalind Y.

, p. 2075 - 2082 (2007/10/02)

The structures and absolute stereochemistry of two moderately toxic jatrophane diterpenes of potential taxonomic importance, esulone A pentadec-4-ene-2,7-dione> and esulone B pentadec-4-ene-2,7-dione>, isolated from Euphorbia esula roots were determined utilizing n.m.r. spectroscopy, X-ray crystallography, and exciton chirality techniques.Stereochemical assignment corrections for previously reported lathyrane and jatrophane diterpenes are discussed.

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