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1(4H)-Naphthalenone, 4-(4-oxo-1(4H)-naphthalenylidene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36378-06-0

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36378-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36378-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,3,7 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36378-06:
(7*3)+(6*6)+(5*3)+(4*7)+(3*8)+(2*0)+(1*6)=130
130 % 10 = 0
So 36378-06-0 is a valid CAS Registry Number.

36378-06-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-oxonaphthalen-1-ylidene)naphthalen-1-one

1.2 Other means of identification

Product number -
Other names [1,1']Binaphthyliden-4,4'-dion

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:36378-06-0 SDS

36378-06-0Upstream product

36378-06-0Downstream Products

36378-06-0Relevant academic research and scientific papers

Electrocatalytic Oxidative Coupling Reaction of Naphthols and Naphthol Ethers on a TEMPO Modified Graphite Felt Electrode

Kashiwagi, Yoshitomo,Ono, Hiroaki,Osa, Tetsuo

, p. 81 - 84 (2007/10/02)

2-Naphthol and 2-methoxynaphthalene were quantitatively oxidized to the corresponding 1,1'-binaphthyls in more than 90percent current efficiency on a graphite felt electrode coated with a thin poly(acrylic acid) layer immobilizing 4-amino-2,2,6,6-tetramethylpiperidinyl-1-oxyl (4-amino-TEMPO). 1-Naphthol and 1-methoxynaphthalene were also completely converted to the predicted 1,1'-, 1,2'-, and 2,2'- positioned coupling products.The reaction proceeds via electrocatalytic oxidation of the modified-TEMPO species.The electrode was not inactivated during electrolysis and could be used repeatedly.

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