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2-(2-oxo-1-phenyl-cyclohexyl)acetic acid is a complex organic compound with the molecular formula C15H16O3. It is a white crystalline solid that is derived from the cyclohexane ring structure, with a phenyl group attached to the second carbon and an acetic acid group at the second position. 2-(2-oxo-1-phenyl-cyclohexyl)acetic acid is characterized by its unique structure, which includes a ketone group (C=O) within the cyclohexane ring and a carboxyl group (COOH) at the end of the molecule. It is used in the synthesis of various pharmaceuticals and chemical intermediates due to its versatile chemical properties and potential for further functionalization. The compound's stability and reactivity make it a valuable building block in organic chemistry, particularly in the development of new drugs and materials.

3645-89-4

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3645-89-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3645-89-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,4 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3645-89:
(6*3)+(5*6)+(4*4)+(3*5)+(2*8)+(1*9)=104
104 % 10 = 4
So 3645-89-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H16O3/c15-12-8-4-5-9-14(12,10-13(16)17)11-6-2-1-3-7-11/h1-3,6-7H,4-5,8-10H2,(H,16,17)

3645-89-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-oxo-1-phenylcyclohexyl)acetic acid

1.2 Other means of identification

Product number -
Other names 2-Phenylcyclohexanon-2-acetic-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

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More Details:3645-89-4 SDS

3645-89-4Relevant academic research and scientific papers

HEXAHYDROINDOLES AND TETRAHYDRO-1H-1-PYRINDINES: ALTERNATIVE FORMATION FROM 5-CARBOXAMIDOPENTANOIC ACIDS AND PROOF OF STRUCTURES

Metz, Gunter

, p. 4101 - 4124 (2007/10/02)

Under mild temperatures the 3-acetyl-3-aryl-5-carboxamidopentanoic acids 1 (Ar=phenyl or dimethoxyphenyl) easily undergo cyclisation in sulfuric acid or polyphosphoric acid (PPA) to the bicyclic lactamlactones 2.Surprisingly different lactams were obtaine

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