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1-Naphthalenecarboxylic acid, 1,2,3,4-tetrahydro-4-oxo-1-phenyl-, also known as 1-(1-Naphthyl)-1,2,3,4-tetrahydro-4-oxopyridine-3-carboxylic acid, is a complex organic compound with the molecular formula C17H15NO3. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, and features a pyridine ring fused to the naphthalene structure. 1-Naphthalenecarboxylic acid, 1,2,3,4-tetrahydro-4-oxo-1-phenyl- is characterized by its unique chemical structure, which includes a phenyl group attached to the naphthalene core, a tetrahydro-4-oxopyridine ring, and a carboxylic acid functional group. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its versatile chemical properties and potential for further functionalization.

2997-25-3

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2997-25-3 Usage

Chemical class

Naphthalene carboxylic acids These are organic compounds containing a naphthalene ring with a carboxylic acid functional group.

Appearance

White to off-white crystalline powder This describes the physical form and color of the compound, which can be important for its handling and identification.

Anti-inflammatory properties

Known to reduce inflammation This property makes the compound potentially useful in treating conditions characterized by swelling and redness.

Analgesic properties

Capable of relieving pain This characteristic makes the compound a potential candidate for pain management applications.

Inhibition of cyclooxygenase enzyme

Acts as an inhibitor of this enzyme, which is involved in the production of prostaglandins This action contributes to the compound's anti-inflammatory and analgesic properties.

Synthesis of pharmaceuticals

Often used in the synthesis of various pharmaceuticals This indicates the compound's importance in the production of medications.

Potential treatment for inflammatory conditions

Studied for its potential use in treating such conditions This highlights the compound's potential therapeutic applications.

Value for medicinal and research purposes

Its chemical structure and properties make it a valuable compound in these fields This emphasizes the importance of the compound in both the development of new medications and scientific research.

Check Digit Verification of cas no

The CAS Registry Mumber 2997-25-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,9 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2997-25:
(6*2)+(5*9)+(4*9)+(3*7)+(2*2)+(1*5)=123
123 % 10 = 3
So 2997-25-3 is a valid CAS Registry Number.

2997-25-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-oxo-1-phenyl-1,2,3,4-tetrahydro-1-naphthalenecarboxylic acid

1.2 Other means of identification

Product number -
Other names 4-oxo-1-phenyl-1,2,3,4-tetrahydronaphthalene-1-carboxylic 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:2997-25-3 SDS

2997-25-3Relevant academic research and scientific papers

Studies in Friedel-Crafts Reaction: Part II-Friedel-Crafts Reaction of 2,2-Diphenylpentanedioic Anhydride

Joshi, U. R.,Khadilkar, B. M.,Samant, S. D.

, p. 75 - 76 (2007/10/02)

2,2-Diphenylpentanedioic anhydride (5) on Friedel-Crafts reaction in nitrobenzene in the presence of AlCl3 gives 4-oxo-1-phenyl-1,2,3,4-tetrahydronaphthalene-1-carboxylic acid (6) as the major product along with 4,4-diphenylbut-3-enoic acid (7).The same r

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