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DIATOXANTHIN is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31063-73-7

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31063-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31063-73-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,0,6 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 31063-73:
(7*3)+(6*1)+(5*0)+(4*6)+(3*3)+(2*7)+(1*3)=77
77 % 10 = 7
So 31063-73-7 is a valid CAS Registry Number.

31063-73-7 Well-known Company Product Price

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  • Sigma-Aldrich

  • (79449)  Diatoxanthin  analytical standard

  • 31063-73-7

  • 79449-1MG

  • 9,143.55CNY

  • Detail

31063-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R)-4-[(1E,3E,5E,7E,9E,11E,13E,15E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15-octaen-17-ynyl]-3,5,5-trimethylcyclohex-3-en-1-ol

1.2 Other means of identification

Product number -
Other names Diatoxanthin/ 7,8-Didehydrozeaxanthin

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:31063-73-7 SDS

31063-73-7Downstream Products

31063-73-7Relevant academic research and scientific papers

Total Synthesis of Acetylenic Carotenoids. 2. Synthesis of (all-E)-(3R,3'R)-Diatoxanthin and (all-E)-(3R)-7,8-Didehydrocryptoxanthin

Haugan, Jarle Andre,Liaaen-Jensen, Synnoeve

, p. 899 - 904 (2007/10/02)

Optically active (all-E)-(3R,3'R)-diatoxanthin, indistinguishable from the natural carotenol, has been prepared by total synthesis for the first time with 34percent overall yield in four steps from the available (2E)-5-(4R)-4-hydroxy-2,6,6-trimethylcyclo

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