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10579-63-2

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10579-63-2 Usage

Chemical class

Isoquinolinone derivatives

Physical state

Yellow solid

Molar mass

221.29 g/mol

Biological activities

Exhibits antifungal and antimicrobial properties

Pharmaceutical applications

Potential use in the development of new drugs

Industrial applications

Used in the synthesis of organic compounds

Occurrence

Found in research laboratories and chemical industries

Chemical structure

Consists of a double bond attached to a ketone functional group and a heterocyclic isoquinoline ring

Utility

Serves as a valuable building block for the preparation of diverse chemical structures

Check Digit Verification of cas no

The CAS Registry Mumber 10579-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,7 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10579-63:
(7*1)+(6*0)+(5*5)+(4*7)+(3*9)+(2*6)+(1*3)=102
102 % 10 = 2
So 10579-63-2 is a valid CAS Registry Number.

10579-63-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,4-dihydro-1H-isoquinolin-2-yl)-2-methylprop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2-(2-methyl-acryloyl)-1,2,3,4-tetrahydro-isoquinoline

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:10579-63-2 SDS

10579-63-2Downstream Products

10579-63-2Relevant articles and documents

Radical cascade involving a 5-endo-trig cyclization of α-amidoyl radicals

Ishibashi, Hiroyuki,Ishita, Atsuko,Tamura, Osamu

, p. 473 - 475 (2002)

Bu3SnH-mediated radical reactions of aryl bromides 4 gave pyrrolo[1,2-b]- and isoindolo[2,1-b]isoquinoline derivatives 11 through a radical cascade process involving a 6-endo-trig cyclization of an aryl radical and a 5-endo-trig cyclization of

Ink, ink cartridge, ink jet recording device, ink jet ink printed matter, compound, and composition

-

Page/Page column 42, (2017/04/04)

Ink contains at least one of a compound represented by the following chemical formula 1, a compound represented by chemical formula 2, a compound represented by chemical formula 3, or a compound represented by chemical formula 4.

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