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1144-20-3

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1144-20-3 Usage

Uses

4-Hydroxy-2-phenylquinoline (cas# 1144-20-3) is a useful bacterial efflux pump inhibitor.

Synthesis Reference(s)

Journal of the American Chemical Society, 68, p. 1270, 1946 DOI: 10.1021/ja01211a041

Check Digit Verification of cas no

The CAS Registry Mumber 1144-20-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,4 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1144-20:
(6*1)+(5*1)+(4*4)+(3*4)+(2*2)+(1*0)=43
43 % 10 = 3
So 1144-20-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H11NO/c17-15-10-14(11-6-2-1-3-7-11)16-13-9-5-4-8-12(13)15/h1-10H,(H,16,17)

1144-20-3SDS

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 2-Phenylquinolin-4-ol

1.2 Other means of identification

Product number -
Other names 2-Phenyl-quinolin-4-ol

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:1144-20-3 SDS

1144-20-3Relevant articles and documents

An efficient oxidation of 2-aryl-1,2,3,4-tetrahydro-4-quinolones employing ferric chloride hexahydrate-methanol: Synthesis of naturally occurring 4-alkoxy-2-arylquinolines

Kumar, K. Hemanth,Muralidharan,Perumal

, p. 7903 - 7906 (2004)

A simple, inexpensive and efficient oxidation of 2-aryl-1,2,3,4-tetrahydro- 4-quinolones has been carried out by employing FeCl3·6H 2O-methanol under mild conditions. This method has been investigated for the synthesis of an endothel

Palladium catalyzed hydrodefluorination of fluoro-(hetero)arenes

Gair, Joseph J.,Grey, Ronald L.,Giroux, Simon,Brodney, Michael A.

supporting information, p. 2482 - 2487 (2019/04/10)

Palladium catalyzed hydrodefluorination was developed for fine-tuning the properties of fluoro-(hetero)aromatic compounds. The robust reaction can be set up in air, requires only commercially available components, and tolerates a variety of heterocycles and functionalities relevant to drug discovery. Given the prevalence of fluorine incorporation around metabolic hotspots, the corresponding deuterodefluorination reaction may prove useful for converting fluorinated libraries to deuterated analogues to suppress the oxidative metabolism by kinetic isotope effects.

Enzymatic resolution of 1-amino-2-vinylcyclopropyl caboxylic acid methyl ester

-

, (2008/06/13)

An enantiomeric-resolving process for obtaining (1R,2S)-1-amino-2-vinylcyclopropyl carboxylic acid methyl ester by use of an esterase, and especially Alcalase?, is disclosed.

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