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110835-84-2

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110835-84-2 Usage

General Description

(1R,2R)-1,2-Dihydrotriphenylene-1,2-diol is a chemical compound with the molecular formula C18H14O2. It is a diol, meaning it contains two hydroxyl groups (-OH) attached to carbon atoms in the molecule. (1R,2R)-1,2-Dihydrotriphenylene-1,2-diol has a unique three-ring structure, with three connected benzene rings. It is a colorless solid at room temperature and is sparingly soluble in water. This chemical has potential applications in organic synthesis and materials science due to its unique structure and reactivity. Studies have also shown that (1R,2R)-1,2-Dihydrotriphenylene-1,2-diol may have potential pharmacological properties, making it an interesting molecule for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 110835-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,8,3 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 110835-84:
(8*1)+(7*1)+(6*0)+(5*8)+(4*3)+(3*5)+(2*8)+(1*4)=102
102 % 10 = 2
So 110835-84-2 is a valid CAS Registry Number.

110835-84-2SDS

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 (1R,2R)-1,2-Dihydro-1,2-triphenylenediol

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:110835-84-2 SDS

110835-84-2Relevant 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.

Efficient Synthesis of Non-K-Region trans-Dihydro Diols of Polycyclic Aromatic Hydrocarbons from o-Quinones and Catechols

Platt, Karl L.,Oesch, Franz

, p. 265 - 268 (2007/10/02)

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