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Cyclooctanol, phenylcarbamate is a chemical compound with the molecular formula C15H21NO2. It is a derivative of cyclooctanol, an eight-carbon cyclic alcohol, and phenylcarbamic acid, which is formed by the reaction of cyclooctanol with phenyl isocyanate. Cyclooctanol, phenylcarbamate is known for its potential applications in pharmaceuticals and agrochemicals, particularly as an intermediate in the synthesis of various biologically active molecules. It is characterized by its unique cyclic structure and the presence of an amide group, which contributes to its reactivity and potential use in the formation of complex organic molecules.

6388-21-2

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6388-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6388-21-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,8 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6388-21:
(6*6)+(5*3)+(4*8)+(3*8)+(2*2)+(1*1)=112
112 % 10 = 2
So 6388-21-2 is a valid CAS Registry Number.

6388-21-2SDS

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 cyclooctanol,phenylcarbamic acid

1.2 Other means of identification

Product number -
Other names Cyclooctanol,phenylcarbamate

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 -
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More Details:6388-21-2 SDS

6388-21-2Downstream Products

6388-21-2Relevant academic research and scientific papers

Selectivity of the biooxygenation of N-phenylcarbamates by the fungus Beauveria bassiana

Pietz, Sylke,Woelker, Doerthe,Haufe, Guenter

, p. 17067 - 17078 (2007/10/03)

The biotransformation with Beauveria bassiana of syn-1,5-dimethylbicyclo[3.2.1]oct-8-yl-N-phenylcarbamate (11), its anti-isomer 13 and cyclooctyl-N-phenylcarbamate 31 is described. Based on the observed hydroxylation positions and on earlier results of ox

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