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57443-82-0

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57443-82-0 Usage

Class

Dihydroxyaromatic ethers

Use

Research tool in neuroscience

Function

Blocks the activity of certain enzymes involved in the metabolism of neurotransmitters

Enzyme Inhibition

Inhibits poly(ADP-ribose) polymerase (PARP)

Role of PARP

Involved in DNA repair and cell survival

Potential Applications

Treatment of neurodegenerative diseases and cancer

Mechanism

Protects neurons from damage and inhibits the growth of cancer cells

Additional Properties

Investigated for anti-inflammatory and antioxidant properties

Therapeutic Applications

Versatile compound with potential use in various fields of medicine

Check Digit Verification of cas no

The CAS Registry Mumber 57443-82-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,4 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57443-82:
(7*5)+(6*7)+(5*4)+(4*4)+(3*3)+(2*8)+(1*2)=140
140 % 10 = 0
So 57443-82-0 is a valid CAS Registry Number.

57443-82-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-diphenyl-2-quinolin-3-ylethanol

1.2 Other means of identification

Product number -
Other names 1,1-diphenyl-2-quinolin-3-yl-ethanol

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:57443-82-0 SDS

57443-82-0Downstream Products

57443-82-0Relevant articles and documents

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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