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68151-04-2

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68151-04-2 Usage

General Description

(1R,2R)-1,2-dihydrotriphenylene-1,2-diol is a compound with the molecular formula C18H14O2. It is a dihydroxy derivative of triphenylene, which is a polycyclic aromatic hydrocarbon. (1R,2R)-1,2-dihydrotriphenylene-1,2-diol is a white solid at room temperature and is sparingly soluble in water. It has been studied for its potential use in organic synthesis and the formation of new materials due to its unique chemical structure and reactivity. As a diol, it contains two hydroxyl groups, making it potentially useful for the formation of polymers and other organic compounds. Overall, (1R,2R)-1,2-dihydrotriphenylene-1,2-diol is a compound of interest in the field of organic chemistry and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 68151-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,5 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 68151-04:
(7*6)+(6*8)+(5*1)+(4*5)+(3*1)+(2*0)+(1*4)=122
122 % 10 = 2
So 68151-04-2 is a valid CAS Registry Number.

68151-04-2SDS

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 trans-1,2-Dihydroxy-1,2-dihydrotriphenylen

1.2 Other means of identification

Product number -
Other names -

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

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More Details:68151-04-2 SDS

68151-04-2Relevant articles and documents

Stereocontrolled synthesis of syn- and anti-diol epoxide metabolites of triphenylene

Koreeda, Masato,Gopalaswamy, Ramesh,Yang, Jinhai,Tuinman, Roeland J.

, p. 8267 - 8270 (2007/10/03)

The synthesis of both syn- and anti-diol epoxide metabolites of triphenylene has been achieved under complete stereochemical control commencing with commercially available 9-phenanthrol in 18% (9 steps) and 37% (8 steps) overall yields, respectively. The exceptionally high stereoselectivity of the dimethyldioxirane oxidation of trans-dihydrodiol having the quasi-diaxially disposed hydroxyl groups is particularly noteworthy.

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