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1H-Cyclopenta[b]quinoxaline, 2,3-dihydro- is a heterocyclic organic compound with the molecular formula C9H10N2. It is a derivative of quinoxaline, which is a fused bicyclic compound consisting of a benzene ring and a pyrazine ring. The 2,3-dihydro prefix indicates that the compound has two hydrogen atoms added to the quinoxaline structure, resulting in a saturated ring system. 1H-Cyclopenta[b]quinoxaline, 2,3-dihydro- is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals and other chemical products due to its unique structure and properties.

7193-24-0

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7193-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7193-24-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,9 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7193-24:
(6*7)+(5*1)+(4*9)+(3*3)+(2*2)+(1*4)=100
100 % 10 = 0
So 7193-24-0 is a valid CAS Registry Number.

7193-24-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dihydro-1H-cyclopenta[b]quinoxaline

1.2 Other means of identification

Product number -
Other names 2,3-dihydro-1H-cyclopenta[b]chinoxalin

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:7193-24-0 SDS

7193-24-0Relevant academic research and scientific papers

Radical annulations with nitriles: Novel cascade reactions of cyano- substituted alkyl and sulfanyl radicals with isonitriles

Camaggi, Carlo Maurizio,Leardini, Rino,Nanni, Daniele,Zanardi, Giuseppe

, p. 5587 - 5598 (2007/10/03)

New radical annulation reactions are described involving addition of cyano-substituted alkyl and sulfanyl radicals to aromatic isonitriles. The tandem cyclisation of the resulting imidoyl radicals onto the cyano group affords cyclopenta- and thienoquinoxalines, respectively. The intervention of the isonitriles in the aromatisation process of the cyclohexadienyl radicals is discussed, as well as the regiochemistry of the cyclisation of the iminyl radicals obtained by addition of the imidoyls to the nitrile moiety. The hypothesis of an exclusive 6-membered ring closure onto the aromatic ring is also supported by the results of semiempirical AM1 calculations.

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