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Phenylalanine, N,N-diethyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61533-14-0

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61533-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61533-14-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,3 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61533-14:
(7*6)+(6*1)+(5*5)+(4*3)+(3*3)+(2*1)+(1*4)=100
100 % 10 = 0
So 61533-14-0 is a valid CAS Registry Number.

61533-14-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(N,N-diethylamino)-3-phenylpropanoate

1.2 Other means of identification

Product number -
Other names 2-Diethylamino-3-phenyl-propionic acid 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:61533-14-0 SDS

61533-14-0Downstream Products

61533-14-0Relevant academic research and scientific papers

Transformations des enamines α-formylees: Synthese d'α-amino esters N,N-disubstitues

Rulev, Alexander Yu.,Larina, Lyudmila I.,Voronkov, Mikhail G.

, p. 10211 - 10214 (2000)

2-Dialkylaminoalkanoic esters are prepared in moderate yield by the reaction of N,N-disubstituted 2-amino-2-alkenals with dialkyl phosphonates in the presence of sodium alkoxide. A mechanism involving an α-keto-β-aminophosphonate as an intermediate is proposed. (C) 2000 Elsevier Science Ltd.

Copper-catalyzed amination of ketene silyl acetals with hydroxylamines: Electrophilic amination approach to α-amino acids

Matsuda, Naoki,Hirano, Koji,Satoh, Tetsuya,Miura, Masahiro

, p. 11827 - 11831 (2013/01/15)

Role reversal: The title reaction has been developed to deliver α-amino acids under very mild reaction conditions (see scheme; dpppen=1,5-bis(diphenylphosphino)pentane). The catalysis provides a new C-N bond-forming approach for the synthesis of α-amino a

SYNTHESE ORGANOMETALLIQUE D'α-AMINOESTERS N,N-DISUBSTITUES

Bourhis, Mireille,Bosc, Jean-Jacques,Golse, Rene

, p. 193 - 202 (2007/10/02)

Reaction of organozinc compounds with a particular gem-aminoether ester, i.e. methyl-N,N-diethylamino methoxyacetate, leads to α-aminoesters.This method allows the synthesis of compounds having potential biological activity, viz. β-unsaturated α-aminoesters.

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