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1-Naphthalenecarboxylic acid, 3-methyl-, also known as 3-Methyl-1-naphthoic acid, is an organic compound with the chemical formula C11H10O2. It is a white crystalline solid that is derived from naphthalene, a polycyclic aromatic hydrocarbon. 1-Naphthalenecarboxylic acid, 3-methyl- is characterized by a carboxylic acid functional group attached to the 1-position of the naphthalene ring and a methyl group at the 3-position. It is used as an intermediate in the synthesis of various pharmaceuticals, dyes, and other organic compounds. Due to its reactivity and potential applications, 3-Methyl-1-naphthoic acid is an important chemical in the field of organic synthesis and industrial chemistry.

5774-05-0

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5774-05-0 Usage

Derived from

Naphthalene (polycyclic aromatic hydrocarbon)

Uses

Synthesis of pharmaceuticals, agrochemicals, and dyes; intermediate in production of other organic compounds; potential applications in nanotechnology

Studied for

Antimicrobial, anti-inflammatory, and antioxidant properties

Precautions

May pose health and environmental risks if not handled properly

Check Digit Verification of cas no

The CAS Registry Mumber 5774-05-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,7 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5774-05:
(6*5)+(5*7)+(4*7)+(3*4)+(2*0)+(1*5)=110
110 % 10 = 0
So 5774-05-0 is a valid CAS Registry Number.

5774-05-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name acide methyl-2 naphtoique-4

1.2 Other means of identification

Product number -
Other names 2-Methyl-4-naphthylsaeure

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:5774-05-0 SDS

5774-05-0Upstream product

5774-05-0Relevant academic research and scientific papers

Electron Transfer Activation - A Selective Photooxidation Method for the Preparation of Aromatic Adehydes and Ketones

Santamaria, Jean,Jroundi, Rachid

, p. 4291 - 4294 (2007/10/02)

A selective and mild photocatalytic procedure for benzylic oxydations with 9,10-dicyanoanthracene (DCA), an usual electron acceptor, in presence of methyl viologen (MV2+) and FeCl2 has been developped.Key words: Singlet Electron Transfer; benzylic oxidation; hydroperoxides

ELECTRON TRANSFER ACTIVATION. HYDROPEROXIDE INTERMEDIATES IN A NOVEL AND SELECTIVE PROCEDURE FOR BENZYLIC OXIDATIONS.

Santamaria, J.,Jroundi, R.,Rigaudy, J.

, p. 4677 - 4680 (2007/10/02)

A selective and mild photochemical procedure for benzylic oxidations with 9,10-dicyanoanthracene (DCA) an usual electron acceptor, in the presence of methyl viologen (MV2+), an electron relay, has been developed.Methyl and methylene groups are oxidized in good to excellent yields to the corresponding hydroperoxides.

PHOTOOXYGENATIONS PAR TRANSFERT D'ELECTRON SENSIBILISEES PAR LE DICYANO-9,10 ANTHRACENE. ROLE DU SOLVANT ET FORMATION D'OXYGENE SINGULET.

Santamaria, J.,Gabillet, P.,Bokobza, L.

, p. 2139 - 2142 (2007/10/02)

Photooxygenation of naphtalenic compounds sensitized by electron acceptors like 9,10 dicyanoanthracene (DCA) is shown to proceed by two distinct ways depending on the solvent polarity.In a polar solvent superoxide ion (O2-.) as well as singlet oxygen (1O2*) are involved while in a non polar solvent only singlet oxygen is produced.

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