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70254-42-1

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70254-42-1 Usage

General Description

2-Quinolinol, also known as 2-Hydroxyquinoline, is a heterocyclic compound with the molecular formula C9H7NO. It is a colorless to yellowish crystalline solid that is soluble in alcohol and ether. 2-Quinolinol is commonly used as a chelating agent in the synthesis of pharmaceuticals, pesticides, and metal complexing agents. It has also been studied for its potential antioxidant and antibacterial properties. In addition, 2-Quinolinol is used as a precursor in the production of various organic compounds. Overall, this chemical plays a crucial role in a wide range of industries due to its versatile properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 70254-42-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,2,5 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70254-42:
(7*7)+(6*0)+(5*2)+(4*5)+(3*4)+(2*4)+(1*2)=101
101 % 10 = 1
So 70254-42-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H7NO/c11-9-6-5-7-3-1-2-4-8(7)10-9/h1-6H,(H,10,11)

70254-42-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-QUINOLINOL

1.2 Other means of identification

Product number -
Other names 2-quinolinone

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:70254-42-1 SDS

70254-42-1Relevant articles and documents

Manganese-Promoted Regioselective Direct C3-Phosphinoylation of 2-Pyridones

Chantarojsiri, Teera,Kittikool, Tanakorn,Phakdeeyothin, Kunita,Yotphan, Sirilata

supporting information, p. 3071 - 3078 (2021/07/22)

A highly efficient and regioselective manganese-induced radical oxidative direct C?P bond formation between 2-pyridones and secondary phosphine oxides was developed. The C3-selective phosphinoylation was conveniently achieved through a combination of substoichiometric manganese and persulfate oxidant under mild conditions. Various 3-phosphinoylated pyridone products can be obtained in moderate to high yields. Preliminary mechanistic studies suggest that the reaction is likely to involve a radical pathway induced by catalytically active Mn3+ species.

Iron-Catalyzed ?±,?-Dehydrogenation of Carbonyl Compounds

Zhang, Xiao-Wei,Jiang, Guo-Qing,Lei, Shu-Hui,Shan, Xiang-Huan,Qu, Jian-Ping,Kang, Yan-Biao

supporting information, p. 1611 - 1615 (2021/03/03)

An iron-catalyzed α,β-dehydrogenation of carbonyl compounds was developed. A broad spectrum of carbonyls or analogues, such as aldehyde, ketone, lactone, lactam, amine, and alcohol, could be converted to their α,β-unsaturated counterparts in a simple one-step reaction with high yields.

Solvent-Dependent Cyclization of 2-Alkynylanilines and ClCF2COONa for the Divergent Assembly of N-(Quinolin-2-yl)amides and Quinolin-2(1 H)-ones

Wang, Ya,Zhou, Yao,Ma, Xingxing,Song, Qiuling

supporting information, p. 5599 - 5604 (2021/08/01)

Herein, we present an expedient Cu-catalyzed [5 + 1] cyclization of 2-alkynylanilines and ClCF2COONa to divergent construction of N-(quinolin-2-yl)amides and quinolin-2(1H)-ones by regulating the reaction solvents. Notably, nitrile acts as a solvent and performs the Ritter reactions. ClCF2COONa is used as a C1 synthon in this transformation, which also represents the first example for utilization of ClCF2COONa as an efficient desiliconization reagent. The current protocol involves in situ generation of isocyanide, copper-activated alkyne, Ritter reaction and protonation.

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