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Cyclohexanebutanoic acid, 2-oxo-, also known as 2-oxocyclohexanebutanoic acid, is a chemical compound with the molecular formula C11H18O3. It is a derivative of cyclohexane, a cyclic hydrocarbon, with a butanoic acid chain attached to it. The 2-oxo prefix indicates the presence of a carbonyl group (C=O) at the second carbon atom in the cyclohexane ring. Cyclohexanebutanoic acid, 2-oxo- is an organic acid with potential applications in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its structure and properties make it a versatile building block in organic chemistry, particularly in the development of complex molecules with specific biological activities.

1838-60-4

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1838-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1838-60-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,3 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1838-60:
(6*1)+(5*8)+(4*3)+(3*8)+(2*6)+(1*0)=94
94 % 10 = 4
So 1838-60-4 is a valid CAS Registry Number.

1838-60-4SDS

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 4-(2-oxocyclohexyl)butanoic acid

1.2 Other means of identification

Product number -
Other names Cyclohexanebutanoic acid,2-oxo

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:1838-60-4 SDS

1838-60-4Relevant academic research and scientific papers

Perhydroazulenes. 5. Preparation of Perhydroazul-9(10)-en-4-one

House, Herbert O.,Lee, Joseph H. C.,VanDerveer, Don,Wissinger, Jane E.

, p. 5285 - 5288 (2007/10/02)

An improved procedure for the preparation of perhydroazul-9(10)-en-4-one is described.Crystal structures were determined for two of the reaction intermediates, 1,6-cyclodecanedione and the cyclic diperoxide derived from 1,6-cyclodecanedione.Measurements of 13C NMR data at various temperatures were used to determine an activation free energy of 14.8 kcal/mol at 298 K for interconversion of the two chair conformers of the cyclic diperoxide.

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