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1,5-Naphthalenedicarbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13554-71-7

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13554-71-7 Usage

Appearance

White solid

Solubility

Insoluble in water

Usage

Building block in various chemical reactions

Pharmaceutical industry

Synthesis of various drugs

Dye and pigment industry

Production of dyes, pigments, and fluorescent compounds

Electronic materials

Development of electronic materials

High-performance materials

Precursor in the production of high-performance materials

Importance

Diverse applications in different industries

Check Digit Verification of cas no

The CAS Registry Mumber 13554-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,5 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13554-71:
(7*1)+(6*3)+(5*5)+(4*5)+(3*4)+(2*7)+(1*1)=97
97 % 10 = 7
So 13554-71-7 is a valid CAS Registry Number.

13554-71-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name naphthalene-1,5-dicarbonitrile

1.2 Other means of identification

Product number -
Other names 1,5-Naphthylendicyanid

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:13554-71-7 SDS

13554-71-7Relevant academic research and scientific papers

SRN1 SYNTHESES OF BIS(PHENYLTHIO)- AND DICYANO-NAPHTHALENES VIA DIAZOSULFIDES

Novi, M.,Garbarino, G.,Petrillo, G.,Dell'Erba, C.

, p. 2205 - 2212 (2007/10/02)

The reactions of bromonaphthalenediazonium tetrafluoroborates (6a,b and 11a,b) with sodium benzenethiolate in DMSO give, through the preliminary formation of the corresponding diazosulfides (7a,b and 12a,b) bis(phenylthio)naphthalenes (8a,b and 13a,b) deriving from substitution of both the diazo group and the bromine.Isolated diazosulfides (7a,b and 12a,b) likewise furnish satisfactory yields of dinitriles (9a,b and 14a,b) by reaction with excess tetrabutylammonium cyanide in DMSO under photostimulation by a sunlamp.The intervention of an SRN1 process accounting for the formation of the disubstitution products is postulated.

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