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4859-45-4

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4859-45-4 Usage

Derived from

naphthalene carboxylic acid

Structure

features a benzene ring with two carboxyl groups attached at different positions

Potential applications

pharmaceutical industry

Use in synthesis

building block for the synthesis of novel drug molecules

Current status

precise uses and properties still under investigation

Reasons for interest

unique structure and potential reactivity

Relevance

target for further research and development in organic chemistry and drug discovery

Check Digit Verification of cas no

The CAS Registry Mumber 4859-45-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,5 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4859-45:
(6*4)+(5*8)+(4*5)+(3*9)+(2*4)+(1*5)=124
124 % 10 = 4
So 4859-45-4 is a valid CAS Registry Number.

4859-45-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2'-carboxyphenyl)-1-naphthoic acid

1.2 Other means of identification

Product number -
Other names 2-(2-carboxy-phenyl)-[1]naphthoic acid

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:4859-45-4 SDS

4859-45-4Relevant articles and documents

Organocatalytic aerobic oxidative cleavage of cyclic 1,2-diketones

Gundala, Sivaji,Fagan, Claire-Louise,Delany, Eoghan G.,Connon, Stephen J.

supporting information, p. 1225 - 1228 (2013/07/19)

The first organocatalytic aerobic oxidative cleavage of cyclic 1,2-diketones is reported. The reaction occurs in either aqueous or alcoholic media and is promoted by a simple N-heterocyclic carbene catalyst derived from a 1,2,4-triazolium ion. No strong oxidants are required. The application of the process in a one-pot synthesis of a cyclic anhydride is also possible. Georg Thieme Verlag Stuttgart. New York.

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