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491024-68-1

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491024-68-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 491024-68-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,1,0,2 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 491024-68:
(8*4)+(7*9)+(6*1)+(5*0)+(4*2)+(3*4)+(2*6)+(1*8)=141
141 % 10 = 1
So 491024-68-1 is a valid CAS Registry Number.

491024-68-1SDS

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 4-chloro-2,6-bis[2-((4S)-4-methyl-4,5-dihydro-1,3-oxazol-2-yl)phenyl]carbamoylpyridine

1.2 Other means of identification

Product number -
Other names 4-Chloro-pyridine-2,6-dicarboxylic acid bis-{[2-((S)-4-methyl-4,5-dihydro-oxazol-2-yl)-phenyl]-amide}

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:491024-68-1 SDS

491024-68-1Downstream Products

491024-68-1Relevant articles and documents

Dynamic helical chirality of an intramolecularly hydrogen-bonded bisoxazoline

Preston, Adam J.,Fraenkel, Gideon,Chow, Albert,Gallucci, Judith C.,Parquette, Jon R.

, p. 22 - 26 (2007/10/03)

The synthesis and conformational properties of 2,6-bis-[2-((4S)-4-methyl-4,5-dihydro-1,3-oxazol-2- yl)phenyl]carbam oylpyridines, 2, have been described. Bisoxazoline 2a was prepared in five steps from 2-nitrobenzoyl chloride in an overall yield of 71%. In contrast to related structures such as 1, bisoxazoline 2a exhibits a highly biased P-type helical conformation in solution and in the solid state. In the crystal lattice, 2a further assembles into a left-handed helical superstructure aligned along the crystallographic c axis. The barrier to helical interconversion, as measured by line-shape analysis of the temperature-dependent 1H NMR spectra of thiobenzyl derivative 2b, was determined to be quite low (ΔG? = 12.3 kcal/mol), indicating the presence of a highly dynamic helical chirality.

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