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199617-23-7

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199617-23-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 199617-23-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,6,1 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 199617-23:
(8*1)+(7*9)+(6*9)+(5*6)+(4*1)+(3*7)+(2*2)+(1*3)=187
187 % 10 = 7
So 199617-23-7 is a valid CAS Registry Number.

199617-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethyl-2-iso-propylpyridine

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:199617-23-7 SDS

199617-23-7Downstream Products

199617-23-7Relevant articles and documents

Synthesis of dihydropyridines and pyridines from imines and alkynes via C-H activation

Colby, Denise A.,Bergman, Robert G.,Ellman, Jonathan A.

, p. 3645 - 3651 (2008/10/09)

A convenient one-pot C-H alkenylation/electrocyclization/aromatization sequence has been developed for the synthesis of highly substituted pyridine derivatives from alkynes and α,β-unsaturated N-benzyl aldimines and ketimines that proceeds through dihydropyridine intermediates. A new class of ligands for C-H activation was developed, providing broader scope for the alkenylation step than could be achieved with previously reported ligands. Substantial information was obtained about the mechanism of the reaction. This included the isolation of a C-H activated complex and its structure determination by X-ray analysis; in addition, kinetic simulations using the Copasi software were employed to determine rate constants for this transformation, implicating facile C-H oxidative addition and slow reductive elimination steps.

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