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2,3-Naphthalenedicarboxylic acid, 1-hydroxy-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36112-45-5

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36112-45-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36112-45-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,1 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 36112-45:
(7*3)+(6*6)+(5*1)+(4*1)+(3*2)+(2*4)+(1*5)=85
85 % 10 = 5
So 36112-45-5 is a valid CAS Registry Number.

36112-45-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimethyl 1-Hydroxynaphthalene-2,3-dicarboxylate

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:36112-45-5 SDS

36112-45-5Downstream Products

36112-45-5Relevant academic research and scientific papers

THERMAL ADDITION REACTIONS TO BENZOCYCLOBUTENONES STUDIED BY FLASH PHOTOLYSIS

Schiess, P.,Eberle, M.,Huys-Francotte, M.,Wirz, J.

, p. 2201 - 2204 (2007/10/02)

Ortho-quinoid vinylketenes 2 have been generated thruogh flash photolysis of benzocyclobutenones 1.A kinetic study of intermolecular addition reactions of 2 competing with the recyclization 2 -> 1 reveals strikingly different substituent effects for the addition of methanol and of dienophiles.

Linearly Condensed peri-Hydroxy Aromatic Compounds Derived from the Cycloaddition Reaction of Homophtalic Anhydrides with Dienophiles

Tamura, Yasumitsu,Wada, Akimori,Sasho, Manabu,Kita, Yasuyuki

, p. 2691 - 2697 (2007/10/02)

Thermal treatment of homophthalic anhydrides (1 and 2) with various dienophiles (3-12) caused cycloaddition with spontaneous extrusion of carbon dioxide to give the corresponding linearly condensed peri-hydroxy aromatic compounds (13-23) in considerable yields.A possible mechanism for these reactions is proposed.Keywords - cycloaddition; homophthalic anhydride; thermal reaction; carbon dioxide extrusion; regiocontrolled reaction; linearly condensed phenolic compound; peri-hydroxy aromatic compound; tetracyclic compound

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