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(4-Methoxy-phenyl)-carbamic acid octyl ester, also known as octyl 4-methoxyphenylcarbamate, is an organic compound with the chemical formula C15H23NO3. It is a derivative of carbamic acid, where the phenyl group is substituted with a methoxy group at the para position and the carbamic acid is esterified with an octyl chain. (4-methoxy-phenyl)-carbamic acid octyl ester is characterized by its aromatic structure and long alkyl chain, which may contribute to its potential applications in various chemical or pharmaceutical processes. It is important to note that the specific uses and properties of (4-methoxy-phenyl)-carbamic acid octyl ester would depend on its reactivity, solubility, and other physical and chemical characteristics, which are not detailed in this summary.

93146-34-0

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93146-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93146-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,1,4 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 93146-34:
(7*9)+(6*3)+(5*1)+(4*4)+(3*6)+(2*3)+(1*4)=130
130 % 10 = 0
So 93146-34-0 is a valid CAS Registry Number.

93146-34-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methoxy-phenyl)-carbamic acid octyl ester

1.2 Other means of identification

Product number -
Other names (4-Methoxy-phenyl)-carbamidsaeure-octylester

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:93146-34-0 SDS

93146-34-0Downstream Products

93146-34-0Relevant academic research and scientific papers

The kinetics and mechanism of alcoholysis of symmetrical substituted diphenylureas

Mantrov,Chimishkyan

, p. 738 - 741 (2007/10/03)

The kinetics of the reaction between n-octyl alcohol and symmetrical substituted diphenylureas was studied. An analytic technique based on the use of high-performance liquid chromatography was developed. Substituent and temperature effects on the rate of alcoholysis were determined. The activation and transition state parameters were calculated. A dissociative mechanism of the reaction was suggested.

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