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33631-47-9

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33631-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33631-47-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,6,3 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33631-47:
(7*3)+(6*3)+(5*6)+(4*3)+(3*1)+(2*4)+(1*7)=99
99 % 10 = 9
So 33631-47-9 is a valid CAS Registry Number.
InChI:InChI=1/C22H33NO2/c1-17(8-6-9-18(2)16-21(25)23-14-15-24)11-12-20-19(3)10-7-13-22(20,4)5/h6,8-9,11-12,16,24H,7,10,13-15H2,1-5H3,(H,23,25)/b9-6+,12-11+,17-8+,18-16+

33631-47-9SDS

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 (2E,4E,6E,8E)-N-(2-hydroxyethyl)-3,7-dimethyl-9-(2,6,6-trimethylcyclohexen-1-yl)nona-2,4,6,8-tetraenamide

1.2 Other means of identification

Product number -
Other names 2-hydroxyethyl all-trans-retinamide

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:33631-47-9 SDS

33631-47-9Downstream Products

33631-47-9Relevant articles and documents

Modification of the antitumor effect of doxorubicin by phosphorylated retinoids conjugated to α-fetoprotein

Arsenov,Babitskaya,Vashkevich,Dad'kov,Kisel',Kuz'mitskii,Strel'chenok

, p. 657 - 660 (2001)

-

Synthesis and properties of some 13-cis- and all-trans-retinamides

Shealy,Frye,O'Dell,Thorpe,Kirk,Coburn Jr.,Sporn

, p. 745 - 751 (2007/10/02)

Several 13-cis-retinamides were synthesized from 13-cis-retinoic acid via either 13-cis-retinoyl chloride or 13-cis-1-retinoylimidazole. All-trans-retinoylglycine was prepared from all-trans-retinoyl chloride and ethyl glycinate. Detailed procedures were developed for the preparation of other all-trans-retinamides on a large scale for studies of the chemoprevention of cancer.

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