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23245-63-8

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23245-63-8 Usage

Chemical Class

Naphthalene derivatives

Characteristic Groups

Nitrile group, nitro group

Usage

Synthesis of various organic compounds

Applications

Organic chemistry, material science

Industrial Uses

Building block for pharmaceuticals, agrochemicals, dyes

Biological Applications

Precursor for synthesizing other functionalized naphthalene derivatives

Risks

Health and environmental risks if not properly managed

Check Digit Verification of cas no

The CAS Registry Mumber 23245-63-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,4 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23245-63:
(7*2)+(6*3)+(5*2)+(4*4)+(3*5)+(2*6)+(1*3)=88
88 % 10 = 8
So 23245-63-8 is a valid CAS Registry Number.

23245-63-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-nitronaphthalene-1-carbonitrile

1.2 Other means of identification

Product number -
Other names 4-nitro-[1]naphthonitrile

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:23245-63-8 SDS

23245-63-8Relevant articles and documents

One-step synthesis of 2,9-disubstituted phenanthrenes via Diels-Alder reactions using 1,4-disubstituted naphthalenes as dienophiles

Paredes, Elisa,Biolatto, Betina,Kneeteman, María,Mancini, Pedro

, p. 4601 - 4603 (2002)

The normal electron-demand Diels-Alder reaction between 1,4-disubstituted naphthalenes, nitro being one of these two groups, and 1-methoxy-3-trimethylsililoxy-1,3-butadiene gives hydroxyphenanthrene derivatives, the yields being enhanced by placement of m

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