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Carbamic acid, [2-[(4-azidophenyl)amino]-2-oxoethyl]-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105310-98-3

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105310-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105310-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,3,1 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 105310-98:
(8*1)+(7*0)+(6*5)+(5*3)+(4*1)+(3*0)+(2*9)+(1*8)=83
83 % 10 = 3
So 105310-98-3 is a valid CAS Registry Number.

105310-98-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-azidophenyl)-α-<(tert-butoxycarbonyl)amino>acetamido

1.2 Other means of identification

Product number -
Other names N-(4-azidophenyl)-α-[(tert-butoxycarbonyl)amino]acetamido

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:105310-98-3 SDS

105310-98-3Relevant academic research and scientific papers

Selective Reactions of Azide-Substituted α-Diazo Amides with Olefins and Alcohols Using Rhodium(II) Catalysts

Jeganathan, Alwarsamy,Richardson, Steward K.,Mani, Rajarathnam S.,Haley, Boyd E.,Watt, David S.

, p. 5362 - 5367 (2007/10/02)

The synthesis and addition of azide-substituted α-diazo amides such as N-(4-azidophenyl)-α-diazoacetamide and N-(4-azido-2-hydroxyphenyl)-α-diazoacetamide to olefins and alcohols using either rhodium(II) acetate or preferably rhodium(II) pivalate provided cyclopropanecarboxamides and α-alkoxy amides, respectively, without disrupting the azide functionality.These azide-bearing α-diazo amides are potentially useful in the preparation of photoaffinity cross-linking reagents for studying the mechanism of action of natural products.

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