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30081-72-2

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30081-72-2 Usage

General Description

4-hydroxy-2H-isoquinolin-1-one, also known as quinolin-4(1H)-one, is a chemical compound that belongs to the isoquinolinone family. It is a heterocyclic compound with a hydroxy group attached to the carbon at position 4 of the isoquinolinone ring. 4-hydroxy-2H-isoquinolin-1-one has been investigated for its potential therapeutic applications, including its use as an inhibitor of enzymes involved in various biological processes. It has also been studied for its potential biological activities, such as antioxidant and anti-inflammatory properties. Additionally, 4-hydroxy-2H-isoquinolin-1-one has been used as a building block in the synthesis of various pharmaceutical and agrochemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 30081-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,0,8 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 30081-72:
(7*3)+(6*0)+(5*0)+(4*8)+(3*1)+(2*7)+(1*2)=72
72 % 10 = 2
So 30081-72-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H7NO2/c11-8-5-10-9(12)7-4-2-1-3-6(7)8/h1-5,11H,(H,10,12)

30081-72-2SDS

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 4-hydroxy-2H-isoquinolin-1-one

1.2 Other means of identification

Product number -
Other names 1,4-Dihydroxy-isochinolin

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:30081-72-2 SDS

30081-72-2Relevant articles and documents

Intramolecular [2+2] photocycloaddition of substituted isoquinolones: Enantioselectivity and kinetic resolution induced by a chiral template

Austin, Kerrie A. B.,Herdtweck, Eberhardt,Bach, Thorsten

supporting information; experimental part, p. 8416 - 8419 (2011/10/31)

From simple to complex: Starting from easily accessible isoquinolones 1 (X=Br, OH), complex cyclobutane photoproducts such as compound 2 can be obtained with high enantioselectivity (88-96% ee) through the use of a chiral template. Compound 3, which was i

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