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77123-18-3

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77123-18-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77123-18-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,2 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 77123-18:
(7*7)+(6*7)+(5*1)+(4*2)+(3*3)+(2*1)+(1*8)=123
123 % 10 = 3
So 77123-18-3 is a valid CAS Registry Number.

77123-18-3SDS

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 (-)-trans-(1R,2R)-1,2-dihydroxy-1,2-dihydrochrysene

1.2 Other means of identification

Product number -
Other names (-)-(1R,2R)-1,2-dihydrochrysene-1,2-diol

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:77123-18-3 SDS

77123-18-3Relevant articles and documents

Enantioselective synthesis of (-)-(1R,2R)-1,2-dihydrochrysene-1,2-diol

Lorentzen, Marianne,Sydnes, Magne O.,J?rgensen, K?re B.

, p. 9041 - 9051 (2014)

A general chiral building block containing the 1R,2R-trans-diol moiety was constructed utilizing the stereoselective Shi-epoxidation reaction on a tetralone scaffold assembled by a Negishi cross-coupling on N,N-diethylbenzamide. Further elaboration of thi

Synthesis of the Enantiomeric Bay-Region Diol Epoxides of Benzanthracene and Chrysene

Yagi, Haruhiko,Vyas, Kamlesh P.,Tada, Masao,Thakker, Dhiren R.,Jerina, Donald M.

, p. 1110 - 1117 (2007/10/02)

Both trans-3,4-dihydroxy-3,4-dihydrobenzanthracene and trans-1,2-dihydroxy-1,2-dihydrochrysene are known proximate carcinogens of their respective hydrocarbons.The present study describes the synthesis of their (+)- and (-)-enantiomers as well as the d

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