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51211-94-0

3,4-Heptadiene, 2,2,3,6,6-pentamethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51211-94-0

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51211-94-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51211-94-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,1 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51211-94:
(7*5)+(6*1)+(5*2)+(4*1)+(3*1)+(2*9)+(1*4)=80
80 % 10 = 0
So 51211-94-0 is a valid CAS Registry Number.

51211-94-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,6,6-pentamethylhepta-3,4-diene

1.2 Other means of identification

Product number -
Other names 2,2,3,6,6-pentamethyl-hepta-3,4-diene

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:51211-94-0 SDS

51211-94-0Downstream Products

51211-94-0Relevant articles and documents

Direct Determination of the Enantiomeric Purity of Chiral Trisubstituted Allenes by Using Permethylated Cyclodextrin as a Chiral Solvating Agent

Uccello-Barretta, Gloria,Balzano, Federica,Caporusso, Anna Maria,Salvadori, Piero

, p. 836 - 839 (1994)

The heptakis(2,3,6-tri-O-methyl)-β-cyclodextrin (TRIMEB) has been successfully used as convenient chiral solvating agent to determine the enantiomeric composition of chiral trisubstituted allenes by 1H NMR spectroscopy: the analysis of the effect of the molar ration TRIMEB/allene, temperature, and nature of the solvent allowed us to optimize the experimental conditions to enhance the separation between the signals of the two enantiomers of each allene.

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