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1,4-Isoquinolinedione, 3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23994-23-2

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23994-23-2 Usage

Chemical class

Phenylisoquinolines

Appearance

Yellow solid

Melting point

142-144°C

Usage

Building block in the synthesis of pharmaceuticals and organic compounds

Potential application

Antitumor agent

Biological activities

Studied for therapeutic applications

Check Digit Verification of cas no

The CAS Registry Mumber 23994-23-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,9,9 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23994-23:
(7*2)+(6*3)+(5*9)+(4*9)+(3*4)+(2*2)+(1*3)=132
132 % 10 = 2
So 23994-23-2 is a valid CAS Registry Number.

23994-23-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenylisoquinoline-1,4-dione

1.2 Other means of identification

Product number -
Other names 3-Phenyl-2-azanaphthochinon

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:23994-23-2 SDS

23994-23-2Relevant academic research and scientific papers

Photoinduced α-Cleavage of 2-Azido-2-phenyl-1,3-indandione at Cryogenic Temperatures

Abe, Manabu,Banerjee, Upasana,Gudmundsdottir, Anna D.,Karney, William L.,Krause, Jeanette A.,Sarkar, Sujan K.

supporting information, p. 7885 - 7890 (2020/11/02)

To expand the utility of α-cleavage at cryogenic temperatures, we investigated the photoreactivity of 2-azido-2-phenyl-1,3-indandione (1). EPR spectroscopy revealed that irradiating 1 in 2-methyltetrahydrofuran (mTHF) matrices forms alkylnitrene 32, which has zero-field splitting parameters (D/hc = 1.5837 cm-1 E/hc = 0.0039 cm-1) typical of an alkylnitrene. IR spectroscopy demonstrated that irradiating 1 in argon matrices results in the concurrent formation of 32, imine 3, benzocyclobutenedione 4, and benzonitrile 5.

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