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Propanedioic acid, (acetylamino)[(pentafluorophenyl)methyl]-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18944-76-8

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18944-76-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18944-76-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,4 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18944-76:
(7*1)+(6*8)+(5*9)+(4*4)+(3*4)+(2*7)+(1*6)=148
148 % 10 = 8
So 18944-76-8 is a valid CAS Registry Number.

18944-76-8SDS

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-acetylamino-2-pentafluorophenylmethyl-malonic acid diethyl ester

1.2 Other means of identification

Product number -
Other names (2,3,4,5,6-Pentafluor-benzyl)-acetamido-malonsaeure-diaethylester

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:18944-76-8 SDS

18944-76-8Relevant academic research and scientific papers

The Enantioselective Dakin-West Reaction

Wende, Raffael C.,Seitz, Alexander,Niedek, Dominik,Schuler, S?ren M. M.,Hofmann, Christine,Becker, Jonathan,Schreiner, Peter R.

supporting information, p. 2719 - 2723 (2016/02/27)

Here we report the development of the first enantioselective Dakin-West reaction, yielding α-acetamido methylketones with up to 58 % ee with good yields. Two of the obtained products were recrystallized once to achieve up to 84 % ee. The employed methylimidazole-containing oligopeptides catalyze both the acetylation of the azlactone intermediate and the terminal enantioselective decarboxylative protonation. We propose a dispersion-controlled reaction path that determines the asymmetric reprotonation of the intermediate enolate after the decarboxylation.

Synthesis of Photoactive p-Azidotetrafluorophenylalanine Containing Peptide by Solid-Phase Fmoc Methodology

Redman, James E.,Ghadiri, M. Reza

, p. 4467 - 4469 (2007/10/03)

(Matrix Presented) N-Fmoc-L-p-azidotetrafluorophenylalanine was prepared from achiral starting materials using an acetamidomalonate synthesis and enzymatic resolution. A photoactive peptide containing this fluorinated residue could be assembled using soli

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