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Acetic acid, [(4-bromophenyl)hydroxyamino][(trifluoroacetyl)amino]-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

910579-13-4

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910579-13-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 910579-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,5,7 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 910579-13:
(8*9)+(7*1)+(6*0)+(5*5)+(4*7)+(3*9)+(2*1)+(1*3)=164
164 % 10 = 4
So 910579-13-4 is a valid CAS Registry Number.

910579-13-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl [(4-bromophenyl)(hydroxy)amino][(trifluoroacetyl)amino]acetate

1.2 Other means of identification

Product number -
Other names [(4-bromo-phenyl)-hydroxy-amino]-(2,2,2-trifluoro-acetylamino)-acetic acid tert-butyl ester

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:910579-13-4 SDS

910579-13-4Relevant academic research and scientific papers

Chelated ester enolates as versatile nucleophiles for direct nucleophilic attack on aromatic nitro groups

Stolz, Daniel,Pick, Rigobert,Kazmaier, Uli

, p. 1616 - 1618 (2006)

Chelated amino acid ester enolates react with aromatic nitro compounds at the nitrogen atom. Best results were obtained with TFA-protected glycinates. Georg Thieme Verlag Stuttgart.

Aromatic nitro groups and their reactions with chelated ester enolates

Stolz, Daniel,Kazmaier, Uli,Pick, Rigobert

, p. 3341 - 3347 (2008/09/17)

Chelated amino acid ester enolates react with aromatic nitro compounds in a 1,3-addition mode at the nitro group giving amino acids bearing an aryl(hydroxy)amino side chain. Best results were obtained with trifluoroacetyl-protected glycinates. Two equivalents of enolate are necessary for complete conversion, because one equivalent is oxidized during the reaction. Georg Thieme Verlag Stuttgart.

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