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31570-97-5

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31570-97-5 Usage

Chemical Properties

Off-white Solid

Uses

5-Hydroxyquinolin-2(1H)-one (cas# 31570-97-5) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 31570-97-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,5,7 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 31570-97:
(7*3)+(6*1)+(5*5)+(4*7)+(3*0)+(2*9)+(1*7)=105
105 % 10 = 5
So 31570-97-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H7NO2/c11-8-3-1-2-7-6(8)4-5-9(12)10-7/h1-5,11H,(H,10,12)

31570-97-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxy-1H-quinolin-2-one

1.2 Other means of identification

Product number -
Other names 5-Hydroxycarbostyril

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:31570-97-5 SDS

31570-97-5Relevant articles and documents

Novel synthesis of 1,6-naphthyridin-2(6H)-ones, quinolin-2(1H)-ones, and quino[7,8-f]quinoline-2,9(1H,10H)-dione from common precursors

Singh

, p. 279 - 280 (1992)

1,6-Naphthyridin-2(6H)-ones 3, quinolin-2(1H)-ones 5, and quino[7,8-f]quinoline-2,9(1H,10H)-dione 10 have been synthesized from 5-acyl-6-[2-(dimethylamino)ethenyl]pyridin-2(1H)-ones 1.

SYNTHESIS OF 5-METHOXY-2(1H)-QUINOLINONE

Fernandez, Maria,Cuesta, Elena de la,Avendano, Carmen

, p. 2615 - 2620 (2007/10/02)

Methylation of 5-hydroxy-2(1H)quinolinone (1) is studied.The previous protection of the amide group in 1 is proposed as the more convenient method to obtain 5-methoxy-2(1H)-quinolinone (1a).

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