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Phenol, 2,6-dimethyl-, carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29768-32-9

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29768-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29768-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,7,6 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 29768-32:
(7*2)+(6*9)+(5*7)+(4*6)+(3*8)+(2*3)+(1*2)=159
159 % 10 = 9
So 29768-32-9 is a valid CAS Registry Number.

29768-32-9SDS

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 carbamic acid,2,6-dimethylphenol

1.2 Other means of identification

Product number -
Other names carbamate de 2,6-dimethylphenyle

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:29768-32-9 SDS

29768-32-9Relevant academic research and scientific papers

4-Dodecylbenzenesulfonic acid (DBSA) promoted solvent-free diversity-oriented synthesis of primary carbamates, S-thiocarbamates and ureas

Sardarian, Ali Reza,Inaloo, Iman Dindarloo

, p. 76626 - 76641 (2015/09/22)

A simple and highly efficient solvent-free method for the conversion of alcohols, phenols, thiols and amines to primary carbamates, S-thiocarbamates and ureas in the presence of 4-dodecylbenzenesulfonic acid (DBSA) as a cheap and green Bronsted acid reagent has been described. All products were obtained in good to excellent yields and characterized using FT-IR, 1H- and 13C-NMR, MS and CHNS techniques.

Unprecedented observation of sulfonamides in the transesterification of N-unsubstituted carbamates with sulfonyl chlorides

Dauvergne, Jér?me,Wellington, Kevin,Chibale, Kelly

, p. 43 - 47 (2007/10/03)

Sulfonamides have been identified as by-products in the base-mediated transesterification of N-unsubstituted carbamates with sulfonyl chlorides to give the corresponding sulfonates. A proposed mechanism and the synthesis of hindered 2,6-disubstituted arylsulfonates via this method are also reported.

SYNTHESES A L'AIDE D'HETEROCUMULENES. 4. Action L'Isocyanate De Chlorosulfonyle Sur les Phenols Encombres

Hedayatullah, Mir,Hugueny, Jean Claude

, p. 167 - 172 (2007/10/02)

The synthesis of the N-chlorosulfonylcarbamates derived from seven hindered phenols is described, as well as their hydrolysis giving a high yield of the corresponding simple carbamates, the selective substitution of their chlorine atom by the anilino radi

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