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Glycine, N-(4-phenoxyphenyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51170-24-2

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51170-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51170-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,7 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51170-24:
(7*5)+(6*1)+(5*1)+(4*7)+(3*0)+(2*2)+(1*4)=82
82 % 10 = 2
So 51170-24-2 is a valid CAS Registry Number.

51170-24-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-[(4-phenoxyphenyl)amino]acetate

1.2 Other means of identification

Product number -
Other names (4-Phenoxy-phenylamino)-acetic acid ethyl 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:51170-24-2 SDS

51170-24-2Relevant academic research and scientific papers

Novel pyrrolidine-2,4-dione derivatives containing pharmacophores of both hydrazine and diphenyl ether as potential antifungal agents: Design, synthesis, biological evaluation, and 3D-QSAR study

Hu, Hao-Ran,Wang, An,Qiu, Ling-Ling,Wang, Xiao-Bin,Chen, Min,Lu, Ai-Min,Yang, Chun-Long

, p. 20071 - 20082 (2020)

In order to screen novel fungicide leads, 19 pyrrolidine-2,4-dione derivatives containing the pharmacophores of both hydrazine and diphenyl ether were designed, synthesized, and characterized by FT-IR, 1H NMR, 13C NMR, and HR-MS. The obtained target compo

Access to α-Amino Acid Esters through Palladium-Catalyzed Oxidative Amination of Vinyl Ethers with Hydrogen Peroxide as the Oxidant and Oxygen Source

Ouyang, Lu,Li, Jianxiao,Zheng, Jia,Huang, Jiuzhong,Qi, Chaorong,Wu, Wanqing,Jiang, Huanfeng

supporting information, p. 15926 - 15930 (2017/11/23)

A novel and convenient palladium catalytic system for the synthesis of α-amino acid esters from simple starting materials is reported. Hydrogen peroxide not only acts as the green oxidant, but also as the oxygen source. This strategy for the conversion of amines and vinyl ethers into highly functionalized and structurally diverse α-amino acid esters is characterized by the simplicity of the experimental procedure, mild reaction conditions, high atom economy, scalability, and practicability.

Design and synthesis of novel hydantoin-containing melanin-concentrating hormone receptor antagonists

Balavoine, Fabrice,Malabre, Patrice,Alleaume, Thierry,Rey, Astrid,Cherfils, Valerie,Jeanneton, Olivier,Seigneurin-Venin, Sophie,Revah, Frederic

, p. 3754 - 3759 (2008/02/10)

We report here new chemical series acting as antagonists of melanin-concentrating hormone receptor 1 (MCHR-1). Synthesis and structure-activity relationships are described leading to the identification of compounds with optimized in vitro pharmacological and in vitro ADME profiles. In vivo activity has been demonstrated in animal models of food intake and depression.

Synthesis of New 3-(Phenoxyphenyl)sydnones

Sindler-Kulyk, Marija,Jakopcic, Kresimir,Mance, Ana Dunja

, p. 1013 - 1015 (2007/10/02)

The title compounds were prepared by dehydrocyclization of corresponding substituted N-nitrosoglycines obtained from isomeric o-, m- and p-aminodiphenyl ether with ethyl bromoacetate and subsequent nitrosation of the intermediate N-arylsubstituted glycine

Angiotensin converting enzyme inhibitors: N-substituted monocyclic and bicyclic amino acid derivatives

Stanton,Gruenfeld,Babiarz,Ackerman,Friedmann,Yuan,Macchia

, p. 1267 - 1277 (2007/10/02)

The synthesis of N-(3-mercaptopropionyl)-N-arylglycines (14a-x), -N-arylalanines (15a,b), -N-cycloalkylglycines (16a-k), and -1,2,3,4-tetrahydroisoquinoline-3-carboxylic acids (17a-d), -1,2,3,4-tetrahydroquinoline-2-carboxylic acids (18a-f), and -indoline-2-carboxylic acids (19a-k) is described. In vitro inhibition of angiotensin converting enzyme (ACE) is reported for each compound, and the structure-activity relationship for each series is discussed. The in vivo inhibition of ACE and antihypertensive effects of representative compounds from each series are discussed. The most potent compound, 19d, had an in vitro ACE IC50 of 2.6 x 10-9 M and lowered blood pressure in spontaneous hypertensive rats 85 mm at a dose of 10 mg/kg po.

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