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2-[(dimethylcarbamothioyl)oxy]phenyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13522-31-1

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13522-31-1 Usage

Main properties

1. Chemical formula: C11H13NO3S
2. Molecular weight: 247.29 g/mol
3. Functional groups: Carbamate and thioester
4. Usage: Organic synthesis, formation of amides and esters
5. Toxicity: Irritating to skin and eyes

Specific content

Ester derivative of phenyl acetate
Commonly used in organic synthesis as a reagent
Starting material for the synthesis of pharmaceuticals, agrochemicals, and fine chemicals

Check Digit Verification of cas no

The CAS Registry Mumber 13522-31-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,2 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13522-31:
(7*1)+(6*3)+(5*5)+(4*2)+(3*2)+(2*3)+(1*1)=71
71 % 10 = 1
So 13522-31-1 is a valid CAS Registry Number.

13522-31-1SDS

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 [2-(dimethylcarbamothioyloxy)phenyl] acetate

1.2 Other means of identification

Product number -
Other names N,N-Dimethylthiocarbaminsaeure-O-2-acetoxyphenylester

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:13522-31-1 SDS

13522-31-1Downstream Products

13522-31-1Relevant academic research and scientific papers

Preparation of catechol derivatives

-

, (2008/06/13)

A method of preparing derivatives of aromatic compounds including the catechol function STR1 by replacement of one of the hydroxyls by mercaptan STR2 Cathechol or a multi-ring compound (naphthyl-, anthryl-, phenanthryl-, etc.) containing the catechol function is first reacted with thiophosgene to produce the corresponding dioxole-2-thione STR3 The thione is ammonolyzed to the corresponding hydroxy N,N-disubstituted thionocarbamate STR4 The thionocarbamate is acetylated to STR5 and heated to rearrange the compound to the corresponding thiolcarbamate STR6 Further heating produces the corresponding oxathiol-2-one STR7 which can be hydrolyzed to the corresponding mercaptan STR8

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