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129042-57-5

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129042-57-5 Usage

General Description

DL-3-Amino-3-(2-naphthyl)propionic acid, also known as 2-Naphthalenepropanoic acid, 3-amino-, is a chemical compound with the molecular formula C13H13NO2. It is an amino acid derivative with a unique structural arrangement, featuring both an amino group and a carboxylic acid group attached to a 2-naphthylpropionic acid backbone. DL-3-Amino-3-(2-naphthyl)propionic acid is primarily utilized in organic synthesis and pharmaceutical research, where it may be used as a reagent or precursor in the production of various pharmaceuticals and other organic compounds. Additionally, it may have potential applications in the field of medicinal chemistry and drug development due to its structural features and potential pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 129042-57-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,0,4 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 129042-57:
(8*1)+(7*2)+(6*9)+(5*0)+(4*4)+(3*2)+(2*5)+(1*7)=115
115 % 10 = 5
So 129042-57-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H13NO2/c14-12(8-13(15)16)11-6-5-9-3-1-2-4-10(9)7-11/h1-7,12H,8,14H2,(H,15,16)

129042-57-5SDS

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 DL-3-Amino-3-(2-Naphthyl)Propionic Acid

1.2 Other means of identification

Product number -
Other names 3-amino-3-naphthalen-2-ylpropanoic acid

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:129042-57-5 SDS

129042-57-5Relevant articles and documents

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Rodionow,Kurtew

, (1953)

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Ruthenium-catalyzed asymmetric epoxidation of olefins using H 2O2, part I: Synthesis of new chiral N,N,N,-tridentate pybox and pyboxazine ligands and their ruthenium complexes

Tse, Man Kin,Bhor, Santosh,Klawonn, Markus,Anilkumar, Gopinathan,Jiao, Haijun,Doebler, Christian,Spannenberg, Anke,Magerlein, Wolfgang,Hugl, Herbert,Beller, Matthias

, p. 1855 - 1874 (2008/02/02)

The synthesis of chiral tridentate N,N,N-pyridine-2.6-bisoxazolines 3 (pyhox ligands) and N,N,N-pyridine-2.6-bisoxazines 4 (pyboxazine ligands) is described in detail. These novel ligands constitute a useful tool-box for the application in asymmetric catalysis. Compounds 3 and 4 are conveniently prepared by cyclization of enantiomerically pure α- or β-amino al cohols with dimethyl pyridine-2,6-dicarboximidate. The corresponding ruthenium complexes are efficient asymmetric epoxidation catalysts and have been prepared in good yield and fully char acterized by spectroscopic means. Four of these ruthenium complexes have been characterized by X-ray crystallography. For the first time the molecular structure of a pyboxazine complex (2,6-bis-[(4S)-4-phenyl-5,6- dihydro-4H-[1,3]oxazinyl]pyridine)(pyridine-2,6-dicarboxylate)ruthenium (S)-2aa, is presented.

META-GUANIDINE, UREA, THIOUREA OR AZACYCLIC AMINO BENZOIC ACID DERIVATIVES AS INTEGRIN ANTAGONISTS

-

, (2008/06/13)

The present invention relates to a class of compounds represented by the Formula Ior a pharmaceutically acceptable salt thereof, whereinA ispharmaceutical compositions thereof and methods of using such compounds and compositions as alphavbeta3 antagonists.

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