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46438-07-7

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46438-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 46438-07-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,4,3 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 46438-07:
(7*4)+(6*6)+(5*4)+(4*3)+(3*8)+(2*0)+(1*7)=127
127 % 10 = 7
So 46438-07-7 is a valid CAS Registry Number.

46438-07-7SDS

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 ethyl 2-amino-3-(2-methylphenyl)propanoate

1.2 Other means of identification

Product number -
Other names ETHYL 2-METHYLPHENYLALANINE

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:46438-07-7 SDS

46438-07-7Relevant academic research and scientific papers

Synthesis of unnatural α-amino esters using ethyl nitroacetate and condensation or cycloaddition reactions

Gagnot, Glwadys,Hervin, Vincent,Coutant, Eloi P.,Desmons, Sarah,Baatallah, Racha,Monnot, Victor,Janin, Yves L.

supporting information, p. 2846 - 2852 (2018/11/27)

We report here on the use of ethyl nitroacetate as a glycine template to produce α-amino esters. This started with a study of its condensation with various arylacetals to give ethyl 3-aryl-2-nitroacrylates followed by a reduction (NaBH4 and then zinc/HCl) into α-amino esters. The scope of this method was explored as well as an alternative with arylacylals instead. We also focused on various [2 + 3] cycloadditions, one leading to a spiroacetal, which led to the undesired ethyl 5-(benzamidomethyl)isoxazole-3-carboxylate. The addition of ethyl nitroacetate on a 5-methylene-4,5-dihydrooxazole using cerium(IV) ammonium nitrate was also explored and the synthesis of other oxazole-bearing α-amino esters was achieved using gold(I) chemistry.

Dimeric cinchona ammonium salts with benzophenone linkers: Enantioselective phase transfer catalysts for the synthesis of α-Amino acids

Woo, Seunga,Kim, Yong-Gyun,Lim, Baegeun,Oh, Jiin,Lee, Yeonji,Gwon, Hyeri,Nahm, Keepyung

, p. 2157 - 2160 (2018/02/06)

Chiral phase transfer catalysts of dimeric cinchona ammonium salts linked with a benzophenone bridge showed high enantioselectivity in the α-Alkylation of a glycinate ester under mild industry-Applicable conditions: 0.5 mol% PTC and near equivalents of al

SN2 displacement at the quaternary carbon center: A novel entry to the synthesis of α,α-disubstituted α-amino acids This Letter is dedicated to the late Professor Harry Wasserman, a great chemist as well as a splendid artist

Ishihara, Kotaro,Hamamoto, Hiromi,Matsugi, Masato,Shioiri, Takayuki

supporting information, p. 3169 - 3171 (2015/05/27)

A novel method for the SN2 reaction on quaternary carbon atoms using bis(p-nitrophenyl)phosphorazidate has been developed. Chiral tertiary alcohols were directly converted into the corresponding chiral tertiary azides with complete inversion of configuration. Several α,α-disubstituted α-amino esters or amino acids were prepared through the conversion of azides to the corresponding amines by catalytic hydrogenation.

Method for Preparation of Piperazindione Derivatives

-

Page/Page column 7, (2011/06/26)

A process for preparing piperazinedione derivatives of the formula I in which R1 is hydrogen, alkyl, alkenyl, alkynyl and alkylcarbonyl,R2 is hydrogen, alkyl, alkenyl, C3-C4-alkynyl and C(═O)R11,Rsup

Transforming natural amino acids into α-alkyl-substituted amino acids with the help of the HOF·CH3CN complex

Harel, Tal,Rozen, Shlomo

, p. 6500 - 6503 (2008/02/10)

(Chemical Equation Presented) α-Alkyl amino acids can be efficiently prepared in high yields from the respective amino acids themselves. The key step is the oxidation of the amine function to create the corresponding α-nitro acid in a fast and very high yield reaction followed by phase-transfer alkylation and finally reduction to the desired α-alkyl amino acid. Several such acids containing aromatic rings or additional carboxylic groups and acids with steric hindrance at the α-position are suitable substrates. Several alkyl halides were examined as alkylating agents.

Generation of aziridinyllithiums from sulfinylaziridines with tert- butyllithium: Properties, reactivity, and application to a synthesis of α,α-dialkylamino acid esters and amides including an optically active form

Satoh, Tsuyoshi,Ozawa, Masaki,Takano, Koji,Chyouma, Tosio,Okawa, Akihiro

, p. 4415 - 4425 (2007/10/03)

Aziridinyllithiums were generated from sulfinylaziridines by a sulfoxide-lithium exchange reaction of sulfoxides with tertbutyllithium at low temperature. The generated aziridinyllithiums were found to be stable in THF at below -30°C and they are reactive with several electrophiles such as carbonyl compounds, ethyl chloroformate, and phenyl isocyanate. The reactivities of the aziridinyllithiums having several alkyl groups were investigated. As an extension of this method, a synthesis of α,α- dialkylamino acid esters, including an optically active form, and amides was realized via the aziridinyllithiums. N-Non substituted α,α-dialkylamino acid esters were synthesized starting from N-(4-methoxyphenyl) aldimine. (C) 2000 Elsevier Science Ltd.

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