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773841-83-1

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773841-83-1 Usage

Description

(R)-2-Amino-3-(2-naphthyl)propionic acid ethyl ester, also known as (R)-2-Naphthylalanine ethyl ester, is a chemical compound derived from the chiral amino acid (R)-2-Amino-3-(2-naphthyl)propionic acid. It is characterized by its unique chemical structure, which features a naphthalene ring attached to an amino acid backbone, and an ethyl ester functional group. (R)-2-Amino-3-(2-naphthyl)propionicacidethylester has garnered significant interest in the fields of pharmaceuticals and medicinal chemistry due to its potential therapeutic properties.

Uses

Used in Pharmaceutical Applications:
(R)-2-Amino-3-(2-naphthyl)propionic acid ethyl ester is used as a neuroprotective agent for the treatment of neurodegenerative diseases such as Alzheimer's and Parkinson's. Its potential therapeutic properties are attributed to its ability to protect neurons from damage and degeneration, offering a promising avenue for the development of new drugs to combat these debilitating conditions.
Used in Research Applications:
In the field of medicinal chemistry, (R)-2-Amino-3-(2-naphthyl)propionic acid ethyl ester serves as an important target for further research and development. Its unique chemical structure and biological properties make it a valuable tool for studying the mechanisms underlying various diseases and for the design of novel therapeutic agents.
Used in Anti-inflammatory and Analgesic Applications:
(R)-2-Amino-3-(2-naphthyl)propionic acid ethyl ester has also been investigated for its anti-inflammatory and analgesic effects, making it a potential candidate for the development of new drugs to treat conditions associated with inflammation and pain. Its ability to modulate these biological processes could lead to the creation of more effective treatments for a wide range of medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 773841-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,3,8,4 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 773841-83:
(8*7)+(7*7)+(6*3)+(5*8)+(4*4)+(3*1)+(2*8)+(1*3)=201
201 % 10 = 1
So 773841-83-1 is a valid CAS Registry Number.

773841-83-1SDS

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 ethyl (2R)-2-amino-3-naphthalen-2-ylpropanoate

1.2 Other means of identification

Product number -
Other names -

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:773841-83-1 SDS

773841-83-1Downstream Products

773841-83-1Relevant articles and documents

Synthesis and automated fluorine-18 radiolabeling of new PSMA-617 derivatives with a CuAAC radiosynthetic approach

Iannone, Marco N.,Stucchi, Stefano,Turolla, Elia A.,Beretta, Chiara,Ciceri, Samuele,Chinello, Clizia,Pagani, Lisa,Todde, Sergio,Ferraboschi, Patrizia

, p. 48 - 62 (2022/01/19)

In the last decade, the development of new radiopharmaceuticals for the imaging and therapy of prostate cancer has been a highly active and important area of research, especially focusing on the prostate-specific membrane antigen (PSMA), an antigen which

Pd-catalyzed directed ortho -C-H alkenylation of phenylalanine derivatives

García-Rubia, Alfonso,Laga, Eduardo,Cativiela, Carlos,Urriolabeitia, Esteban P.,Gómez-Arrayás, Ramón,Carretero, Juan C.

, p. 3321 - 3331 (2015/03/30)

A practical Pd-catalyzed ortho-olefination of enantioenriched N-(SO2Py)-protected aryl-alanine and norephedrine derivatives with electron-deficient alkenes has been developed using N-fluoro-2,4,6-trimethylpyridinium triflate as the terminal oxidant. The reaction occurs efficiently with excellent monosubstitution selectivity and without loss of enantiopurity. This cross-coupling proved to be broad in scope, tolerating a variety of steric and electronic changes to both coupling partners. Removal of the directing group under mild conditions provides access to optically active tetrahydroisoquinoline-3-carboxylic acid derivatives (Tics) with good diastereocontrol and with very small erosion of enantiomeric purity.

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