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3-(4-chlorophenyl)-3-pyridin-2-yl-propan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73486-85-8

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73486-85-8 Usage

Pharmacological Properties

Selective agonist for the alpha-7 nicotinic acetylcholine receptor (α7nAChR)
α7nAChR is a ligand-gated ion channel found in the central nervous system

Therapeutic Applications

Studied for potential use in neurological and psychiatric disorders
Alzheimer's disease
Schizophrenia
Cognitive deficits

Specific Activity

Acts specifically on α7nAChR

Drug Development Target

Considered for further research and drug development due to its potential therapeutic effects

Check Digit Verification of cas no

The CAS Registry Mumber 73486-85-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,8 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73486-85:
(7*7)+(6*3)+(5*4)+(4*8)+(3*6)+(2*8)+(1*5)=158
158 % 10 = 8
So 73486-85-8 is a valid CAS Registry Number.

73486-85-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-chlorophenyl)-3-pyridin-2-yl-propan-1-ol

1.2 Other means of identification

Product number -
Other names 3-Hydroxy-1-(4-chlor-phenyl)-1-(pyridyl-(2))-propan

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:73486-85-8 SDS

73486-85-8Downstream Products

73486-85-8Relevant academic research and scientific papers

Ruthenium-catalyzed /V-alkylation of amines and sulfonamides using borrowing hydrogen methodology

Hamid, M. Haniti S. A.,Allen, C. Liana,Lamb, Gareth W.,Maxwell, Aoife C.,Maytum, Hannah C.,et al.

supporting information; experimental part, p. 1766 - 1774 (2009/07/25)

The alkylation of amines by alcohols has been achieved using 0.5 mol percent [Ru(p-cymene)CI2]2 with the bidentate phosphines dppf or DPEphos as the catalyst. Primary amines have been converted into secondary amines, and secondary amines into tertiary amines, including the syntheses of Piribedil, Tripelennamine, and Chlorpheniramine. A/-Heterocyclization reactions of primary amines are reported, as well as alkylation reactions of primary sulfonamides. Secondary alcohols requiremore forcing conditions than primary alcohols but are still effective a lkylating agents in the presence of this catalyst.

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