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3-methylpent-1-yn-3-yl phenylcarbamate is a chemical compound with the molecular formula C14H15NO2. It is a derivative of phenylcarbamic acid, featuring a 3-methylpent-1-yn-3-yl group attached to the carbamate moiety. This alkyne group consists of a five-carbon chain with a methyl group at the third position and a triple bond at the first position. The phenylcarbamate structure is characterized by an amide linkage between a phenol group and an isocyanate group. 3-methylpent-1-yn-3-yl phenylcarbamate is known for its potential applications in the synthesis of various organic compounds and pharmaceuticals, particularly as an intermediate in the preparation of certain agrochemicals and pharmaceuticals. Its unique structure, with the combination of a phenyl group and an alkyne chain, may also be of interest in materials science for the development of new polymers or other advanced materials.

32496-85-8

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32496-85-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32496-85-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,4,9 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 32496-85:
(7*3)+(6*2)+(5*4)+(4*9)+(3*6)+(2*8)+(1*5)=128
128 % 10 = 8
So 32496-85-8 is a valid CAS Registry Number.

32496-85-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylpent-1-yn-3-yl N-phenylcarbamate

1.2 Other means of identification

Product number -
Other names CARBANILIC ACID,3-METHYL-1-PENTYN-3-YL ESTER

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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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:32496-85-8 SDS

32496-85-8Relevant academic research and scientific papers

Regioselective 1,3-dipolar cycloaddition reactions of 4-methylene-2- oxazolidinones with benzonitrile oxide

Newton, Rebecca,Savage, G. Paul

, p. 432 - 437 (2008/09/21)

Substituted 4-methylene-2-oxazolidinones were prepared in two steps by cyclizing O-propargyl carbamates, which in turn were prepared from propargyl alcohols and phenyl isocyanate. The 4-methylene-2-oxazolidinones underwent a 1,3-dipolar cycloaddition reac

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