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N-(4-hydroxy-3-methyl-1-naphthyl)acetamide is a chemical compound with the molecular formula C12H13NO2. It is a derivative of naphthalene, featuring a hydroxyl group at the 4-position, a methyl group at the 3-position, and an amide group attached to the 1-position. N-(4-hydroxy-3-methyl-1-naphthyl)acetamide is known for its potential applications in various fields, including pharmaceuticals and materials science, due to its unique structure and properties. It is often used as an intermediate in the synthesis of more complex molecules or as a building block in the development of new drugs. The compound's specific applications and properties can vary depending on the context in which it is used, highlighting its versatility in chemical research and development.

523-68-2

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523-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 523-68-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 523-68:
(5*5)+(4*2)+(3*3)+(2*6)+(1*8)=62
62 % 10 = 2
So 523-68-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H13NO2/c1-8-7-12(14-9(2)15)10-5-3-4-6-11(10)13(8)16/h3-7,16H,1-2H3,(H,14,15)

523-68-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-hydroxy-3-methylnaphthalen-1-yl)acetamide

1.2 Other means of identification

Product number -
Other names Acetamide, N-(4-hydroxy-3-methyl-1-naphthalenyl)-

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:523-68-2 SDS

523-68-2Downstream Products

523-68-2Relevant academic research and scientific papers

DPPH radical scavenging activity of paracetamol analogues

Alisi, Maria Alessandra,Brufani, Mario,Cazzolla, Nicola,Ceccacci, Francesca,Dragone, Patrizia,Felici, Marco,Furlotti, Guido,Garofalo, Barbara,La Bella, Angela,Lanzalunga, Osvaldo,Leonelli, Francesca,Marini Bettolo, Rinaldo,Maugeri, Caterina,Migneco, Luisa Maria,Russo, Vincenzo

, p. 10180 - 10187 (2013/01/15)

Biochemical studies suggest a direct relationship between the radical scavenging activity of paracetamol (I) and its antipyretic and analgesic action. To evaluate the effect of chemical modifications on the radical scavenging activity of compounds of type I, analogues 1-14 were prepared and submitted to a stable free radical (DPPH; 1,1-diphenyl-2-picryl-hydrazyl) assay. All paracetamol derivatives showed a significant higher efficiency than the parent compound. This study showed that radical scavenging activity can be increased by decreasing the phenolic ortho substituents steric hindrance or by introducing substituents on the acyl moiety like an indazole ring or the ionic N-methyl morpholinium group. A significant activating effect was also observed by replacing the 1,4-acylamidophenol with a 1,4-acylamidonaphthol system.

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