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Butanoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-(methylsulfonyl)-, methyl ester, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

160141-86-6

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160141-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160141-86-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,1,4 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 160141-86:
(8*1)+(7*6)+(6*0)+(5*1)+(4*4)+(3*1)+(2*8)+(1*6)=96
96 % 10 = 6
So 160141-86-6 is a valid CAS Registry Number.

160141-86-6SDS

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 (S)-methyl 2-(tert-butoxycarbonylamino)-4-(methylsulfonyl)butanoate

1.2 Other means of identification

Product number -
Other names N-tert-butoxycarbonyl-L-methionine sulfone methyl 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:160141-86-6 SDS

160141-86-6Relevant academic research and scientific papers

A novel oxidative side-chain transformation of α-amino acids and peptides by methyltrioxorhenium/H2O2 system

Lazzaro, Francesco,Crucianelli, Marcello,De Angelis, Francesco,Neri, Veronica,Saladino, Raffaele

, p. 9237 - 9240 (2004)

N-Boc derivatives of Met, Cys, and Trp, the properties of which resemble those of the respective amino acid residues present in proteins, are efficiently oxidized by methyltrioxorhenium and H2O2. A high regioselectivity for the oxida

INHIBITORS OF THE FIBROBLAST GROWTH FACTOR RECEPTOR

-

, (2015/05/05)

Described herein are inhibitors of FGFR-4, pharmaceutical compositions including such compounds, and methods of using such compounds and compositions.

Facile conversion of cysteine and alkyl cysteines to dehydroalanine on protein surfaces: Versatile and switchable access to functionalized proteins

Bernardes, Goncalo J. L.,Chalker, Justin M.,Errey, James C.,Davis, Benjamin G.

, p. 5052 - 5053 (2008/10/09)

An efficient and robust oxidative elimination of cysteine to dehydroalanine has been discovered. The reaction is induced by O-mesitylenesulfonylhydroxylamine (MSH) and is compatible with methionine. The key elimination has been executed on protein surfaces and allows ready access to different post-translationally modified proteins through conjugate addition of sulfur nucleophiles to dehydroalanine. Treatment of the resulting thioether with MSH results in regeneration of dehydroalanine, allowing a "functional switch" by subsequent addition of a different thiol. Copyright

Amino acid derived thiane oxide and dioxide systems as disposable templates: Synthesis of α-amino ketones, anti-amino alcohols and an amino cyclopentenone

Gamble, Mark P.,Giblin, Gerard M. P.,Montana, John G.,O'Brien, Peter,Ockendon, Timothy P.,Taylor, Richard J. K.

, p. 7457 - 7460 (2007/10/03)

Sulfones and sulfoxides synthesised from methionine and homocysteine thiolactone have been cyclised to amino ketones using potassium bis(trimethylsilyl)amide. Ramberg-Backlund chemistry on one of the sulfones gave an amino cyclopentenone whereas acyclic α-amino ketones and anti-amino alcohols were obtained by Raney nickel desulfurisation of the sulfoxides.

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