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Carbamic acid, (2-methylphenoxy)-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119930-83-5

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119930-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119930-83-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,9,3 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 119930-83:
(8*1)+(7*1)+(6*9)+(5*9)+(4*3)+(3*0)+(2*8)+(1*3)=145
145 % 10 = 5
So 119930-83-5 is a valid CAS Registry Number.

119930-83-5SDS

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 tert-butyl N-(2-methylphenoxy)carbamate

1.2 Other means of identification

Product number -
Other names tert-butyl 2-methylphenoxycarbamate

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:119930-83-5 SDS

119930-83-5Relevant academic research and scientific papers

Iron-mediated synthesis of t-butyl-N-(aryloxy)carbamates

Holden,Cole

, p. 2579 - 2586 (2007/10/02)

The anion of t-butyl-N-hydroxycarbamate displaces halogens from (η6-haloarene)(η5-cyclopentadienyliron) salts. The resulting complexes are demetallated by photolysis in sunlight to generate t-butyl-N-(aryloxy)carbamates.

Nucleophilic Aromatic Substitution on Tricarbonyl(halogenoarene)chromium Complexes: A New Synthesis of O-Arylhydroxylamines

Baldoli, Clara,Buttero, Paola Del,Licandro, Emanuela,Maiorana, Stefano

, p. 344 - 345 (2007/10/02)

A series of O-arylhydroxylamines 4 have been synthesized under mild conditions and in good yields by the reaction of tricarbonyl(halogenoarene)chromium complexes 1 with N-(tert-butyloxycarbonyl)hydroxylamine (tert-butyl N-hydroxycarbamate), followed by decomplexation and acidic hydrolysis of the tert-butyl N-(aryloxy)carbamates 3.

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