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1-Naphthalenecarbonitrile, 2-(phenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52805-40-0

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52805-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52805-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,0 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 52805-40:
(7*5)+(6*2)+(5*8)+(4*0)+(3*5)+(2*4)+(1*0)=110
110 % 10 = 0
So 52805-40-0 is a valid CAS Registry Number.

52805-40-0SDS

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 2-benzyloxy-1-naphthonitrile

1.2 Other means of identification

Product number -
Other names 2-Benzyloxy-naphthonitril

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:52805-40-0 SDS

52805-40-0Downstream Products

52805-40-0Relevant academic research and scientific papers

Metal-Free Regioselective Monocyanation of Hydroxy-, Alkoxy-, and Benzyloxyarenes by Potassium Thiocyanate and Silica Sulfuric Acid as a Cyanating Agent

Sardarian, Ali Reza,Dindarloo Inaloo, Iman,Modarresi-Alam, Ali Reza,Kleinpeter, Erich,Schilde, Uwe

, p. 1748 - 1756 (2019/02/05)

A novel and efficient metal- and solvent-free regioselective para-C-H cyanation of hydroxy-, alkoxy-, and benzyloxyarene derivatives has been introduced, using nontoxic potassium thiocyanate as a cyanating reagent in the presence of silica sulfuric acid (SSA). The desired products are obtained in good to high yields without any toxic byproducts.

Electrochemical C-H cyanation of electron-rich (Hetero)arenes

Hayrapetyan, Davit,Rit, Raja K.,Kratz, Markus,Tschulik, Kristina,Goo?en, Lukas J.

supporting information, p. 11288 - 11291 (2018/10/20)

A straightforward method for the electrochemical C-H cyanation of arenes and heteroarenes that proceeds at room temperature in MeOH, with NaCN as the reagent in a simple, open, undivided electrochemical cell is reported. The platinum electrodes are passivated by ad-sorbed cyanide, which allows conversion of an exceptionally broad range of electron-rich substrates all the way down to dialkyl arenes. The cyanide electrolyte can be replenished with HCN, opening opportunities for salt-free industrial C-H cyanation.

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