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2,3-Quinoxalinediethanol,α2,α2,α3,α3-tetraphenylis a chemical compound that is a tetraphenyl derivative of a quinoxaline compound. This unique structure endows it with distinctive properties and potential applications in various fields. It is known for its stability and reactivity, which make it a promising candidate for research and development in chemistry and materials science.

59417-49-1

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59417-49-1 Usage

Uses

Used in Materials Science:
2,3-Quinoxalinediethanol,α2,α2,α3,α3-tetraphenylis used as a building block for the construction of organic materials. Its tetraphenyl structure contributes to the development of new materials with enhanced properties.
Used in Organic Synthesis:
2,3-Quinoxalinediethanol,α2,α2,α3,α3-tetraphenylis used as a key intermediate in the synthesis of novel pharmaceutical compounds. Its reactivity and stability make it a valuable component in the creation of new drug molecules.
Used in Pharmaceutical Research:
2,3-Quinoxalinediethanol,α2,α2,α3,α3-tetraphenylis used as a potential candidate in the development of new drugs. Its unique chemical structure offers opportunities for the exploration of its therapeutic potential in various medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 59417-49-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,4,1 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 59417-49:
(7*5)+(6*9)+(5*4)+(4*1)+(3*7)+(2*4)+(1*9)=151
151 % 10 = 1
So 59417-49-1 is a valid CAS Registry Number.

59417-49-1SDS

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 2-[3-(2-hydroxy-2,2-diphenylethyl)quinoxalin-2-yl]-1,1-diphenylethanol

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:59417-49-1 SDS

59417-49-1Downstream Products

59417-49-1Relevant academic research and scientific papers

LATERAL METALLATION OF METHYLATED NITROGENOUS HETEROCYCLES

Kaiser, Edwin M.

, p. 2055 - 2064 (2007/10/02)

Me groups on nitrogenous heterocycles can be conveniently metallated by a variety of strongly basic reagents to afford synthetically useful carbanions.The negative charge of such anions resides predominantly on the ring N atoms.The site of lithiation on pyridines and quinolines bearing Me groups in both the 2- and 4-positions depends upon the ability of the ring N atom to complex with the metallating agents.Carbanions derived from methylated pyridines, quinolines, naphthyridines, isoquinolines, pyridocarbazoles, pteridines, pyridoindoles and quinoxalines are discussed.References are provided describing condensations of these reagents with a variety of both common and uncommon electrophiles.

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