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methyl (2,4,6-trimethylphenyl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81517-97-7

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81517-97-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81517-97-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,1 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81517-97:
(7*8)+(6*1)+(5*5)+(4*1)+(3*7)+(2*9)+(1*7)=137
137 % 10 = 7
So 81517-97-7 is a valid CAS Registry Number.

81517-97-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl N-(2,4,6-trimethylphenyl)carbamate

1.2 Other means of identification

Product number -
Other names methyl-N-2,4,6-trimethylphenylcarbamate

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:81517-97-7 SDS

81517-97-7Relevant academic research and scientific papers

Methyltrioxorhenium-catalyzed oxidation of aromatic aldoximes

Cardona, Francesca,Soldaini, Gianluca,Goti, Andrea

, p. 1553 - 1556 (2007/10/03)

The first catalytic oxidation of aryl oximes to nitro compounds by means of methyltrioxorhenium and urea hydroperoxide is reported. The formation of carbamates, probably occurring through formation of nitrile oxide intermediates, has been observed from 2,6-disubstituted aryl oximes.

Thermochemical Study of Complexation of Carbamates with Isocyanates in Solution

Gorbatov,Yablokova,Kheidorov

, p. 1838 - 1839 (2007/10/03)

Complexation of alkyl phenylcarbamates with isocyanates was studied calorimetrically. The compositions, stability constants, and enthalpies of formation of the complexes were determined. The stability of the complexes regularly increases with increasing electron-donor power of substituents in carbamates and electron-acceptor power of isocyanates.

Isocyanates - Part 3. Synthesis of carbamates by DMAP-catalyzed reaction of amines with di-tert-butyldicarbonate and alcohols

Knoelker, Hans-Joachim,Braxmeier, Tobias

, p. 5861 - 5864 (2007/10/03)

Carbamates are prepared by DMAP-catalyzed reaction of amines with di-tert-butyldicarbonate and subsequent trapping of the intermediate isocyanates with alcohols.

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