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3752-42-9

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3752-42-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3752-42-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,5 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3752-42:
(6*3)+(5*7)+(4*5)+(3*2)+(2*4)+(1*2)=89
89 % 10 = 9
So 3752-42-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H9N/c16-10-14-7-3-6-13-8-11-4-1-2-5-12(11)9-15(13)14/h1-9H

3752-42-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name anthracene-1-carbonitrile

1.2 Other means of identification

Product number -
Other names Anthracenecarbonitrile(9CI)

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:3752-42-9 SDS

3752-42-9Relevant articles and documents

1 - [...] synthetic preparation method

-

, (2019/02/13)

The invention discloses a 1 - [...] synthetic preparation method, comprises the following steps: S1) will anthracene and acetyl chloride is dissolved in the solvent, and the catalysis of a Lewis acid, reaction to obtain the 1 - b [...]; S2) 1 - b [...] through oxidation reaction, to obtain 1 - carboxylic acid anthracene; S3) under the action of the acyl, firstly the 1 - anthracene acid radical chloride acid, to remove the surplus solvent, followed by reaction with cyanide, to produce the target compound 1 - cyanate anthracene. The present invention provides 1 - [...] synthetic preparation method, in order to low-cost transfer catalyst, acetyl chloride as the raw material, after three step synthesis of simple and convenient operation, and then after treatment and purification, can prepare and get the purity 98% or more of 1 - [...], not only the production cost is low, the experimental steps are few, simple operation, and after the simple purification, the purity can reach 98% above, can fully meet the T - 2 toxin of the derivatization detection, greatly reduce the T - 2 toxin detection cost.

Tetrachloropyridine: A new reagent for the dehydration of aldoximes under microwave

Lingaiah, Nagarapu,Narender, Ravirala

, p. 2391 - 2394 (2007/10/03)

Dehydration of aldoximes to nitriles using tetrachloropyridine under microwave in dry media is described. The procedure is applicable to a variety of aldoximes and the reagent can be recycled and reused.

Dehydration of aldoximes to nitriles with clay

Meshram

, p. 943 - 944 (2007/10/02)

The dehydration of alkyl, aryl, heterocyclic and polynuclear aldehyde oximes with montmorillonite KSF as catalyst is reported.

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