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472-73-1

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472-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 472-73-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 472-73:
(5*4)+(4*7)+(3*2)+(2*7)+(1*3)=71
71 % 10 = 1
So 472-73-1 is a valid CAS Registry Number.

472-73-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,4E)-4-[(2E,4E,6E,8E,10E,12E,14E,16E,18E)-18-[(4S)-4-hydroxy-2,6,6-trimethylcyclohex-2-en-1-ylidene]-3,7,12,16-tetramethyloctadeca-2,4,6,8,10,12,14,16-octaenylidene]-3,5,5-trimethylcyclohex-2-en-1-ol

1.2 Other means of identification

Product number -
Other names Eschscholtzxanthin

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:472-73-1 SDS

472-73-1Relevant articles and documents

Determination of Enantiomeric Composition of Partly Racemized Carotenols

Aareskjold, Kare,Liaaen-Jensen, Synnove

, p. 499 - 504 (2007/10/02)

Method for determining enantiomeric composition of various racemized carotenols by converting them into diastereomeric esters with subsequent analysis have been studied.Diastereomeric esters of (-)-camphanic acid with carotenols other than α-ketols could not be separated by HPLC.No separation was achieved for diastereomeric esters of methoxytrifluoromethylphenylacetic acid (MTPA). 1H NMR analysis in the presence of Eu(fod)3 of diastereomeric MTPA esters allowed quantitative determination of the enantiomeric composition of carotenols with 2-hydroxy-β- and 3-hydroxy-β-type end groups.

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