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2H-Pyran-3-carbonitrile, 6-(4-chlorophenyl)-4-(4-methyl-1-piperidinyl)-2-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

326859-29-4

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326859-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 326859-29-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,6,8,5 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 326859-29:
(8*3)+(7*2)+(6*6)+(5*8)+(4*5)+(3*9)+(2*2)+(1*9)=174
174 % 10 = 4
So 326859-29-4 is a valid CAS Registry Number.

326859-29-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Cyano-6-(4-chlorophenyl)-4-(4-methylpiperidino)-2H-pyran-2-one

1.2 Other means of identification

Product number -
Other names 6-(4-Chloro-phenyl)-4-(4-methyl-piperidin-1-yl)-2-oxo-2H-pyran-3-carbonitrile

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:326859-29-4 SDS

326859-29-4Downstream Products

326859-29-4Relevant academic research and scientific papers

A facile access to the synthesis of functionalised unsymmetrical biaryls from 2H-pyran-2-ones through carbanion induced C-C bond formation

Ram, Vishnu J.,Nath, Mahendra,Srivastava, Pratibha,Sarkhcl, Sanjay,Maulik, Prakas R.

, p. 3719 - 3723 (2000)

A convenient synthesis of highly functionalised biaryls 3 and 6 has been delineated through carbanion induced C-C bond formation from 6-aryl-3-cyano-4-substituted-2H-pyran-2-ones (1, 4) and acetone. Extension of this reaction, using aromatic ketones led to (4,6-diarylpyran-2-ylidene)acetonitrile (7) in lieu of the anticipated 2,4-diaryl-6-methylthiobenzonitrile (8). The structure of 2-methyl-6-methylthio-4-(3,4-methylenedioxyphenyl)benzonitrile (3f) was ascertained by single crystal X-ray diffraction analysis and displayed a variety of weak interactions, responsible for the stability and packing of the molecule in the crystalline state. The Royal Society of Chemistry 2000.

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