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2,3-Naphthalenedicarbonitrile, 1-hydroxy-4-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79781-50-3

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79781-50-3 Usage

Chemical compound

2,3-Naphthalenedicarbonitrile, 1-hydroxy-4-phenyl-

Main properties

Consists of a naphthalene core
Contains two cyano groups at the 2 and 3 positions
Has a hydroxyl group at the 1 position
Includes a phenyl group at the 4 position

Common uses

Production and synthesis of pharmaceuticals and organic compounds

Applications

Studied in organic chemistry
Potential use as a reagent in chemical reactions

Research focus

Biological activity
Pharmacological properties

Fields of interest

Medicinal chemistry
Drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 79781-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,8 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 79781-50:
(7*7)+(6*9)+(5*7)+(4*8)+(3*1)+(2*5)+(1*0)=183
183 % 10 = 3
So 79781-50-3 is a valid CAS Registry Number.

79781-50-3SDS

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 4-phenyl-2,3-dicyano-1-naphthol

1.2 Other means of identification

Product number -
Other names -

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:79781-50-3 SDS

79781-50-3Relevant academic research and scientific papers

SOME DERIVATIVES OF 4-ARYL-2,3-DICYANO-1-NAPHTHOL

Krepelka, Jiri,Vancurova, Iva,Holubek, Jiri

, p. 1523 - 1529 (2007/10/02)

Reactions of vicinal aromatic dibromo derivatives Ia-d with the system copper(I)cyanide-tetramethylurea gave vicinal dicyano derivatives IIa-d; products of partial substitution, Va-d, demethylation and deacetylation, IIIa-c, were also formed.The compounds IIIa-c were also prepared by direct demethylation of compounds IIa-c with the system anhydrous aluminium chloride-dichloroethane.The structures of selected compounds were determined by spectral methods.Compounds IIa-d have proved to have a moderate antineoplastic effect in animals with some transplantable experimental tumours.

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