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153973-14-9

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153973-14-9 Usage

Type of compound

A hydrochloride salt of 2-amino-N-phenylpropanamide

Derivation

Derived from the amino acid phenylalanine

Potential uses

Analgesic and anti-inflammatory agent, studied for the treatment of various types of pain and inflammation

Form

Hydrochloride salt

Properties

Stability and solubility

Status

Potential as a new drug candidate for the treatment of pain and inflammatory conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 153973-14-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,9,7 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 153973-14:
(8*1)+(7*5)+(6*3)+(5*9)+(4*7)+(3*3)+(2*1)+(1*4)=149
149 % 10 = 9
So 153973-14-9 is a valid CAS Registry Number.

153973-14-9SDS

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 2-Amino-N-phenylpropanamide hydrochloride

1.2 Other means of identification

Product number -
Other names 2-Amino-Propionylanilide Hydrochloride

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:153973-14-9 SDS

153973-14-9Downstream Products

153973-14-9Relevant articles and documents

Enantioselective Deaminative Alkylation of Amino Acid Derivatives with Unactivated Olefins

Cai, Yue-Ming,Martin, Ruben,Rui, Xi-Yan,Shang, Ming,Sun, Shang-Zheng,Wang, Jia-Bao,Yao, Hong-Qing,Zhang, De-Liang

supporting information, p. 1130 - 1137 (2022/02/05)

Herein, we report the first Ni-catalyzed enantioselective deaminative alkylation of amino acid and peptide derivatives with unactivated olefins. Key for success was the discovery of a new sterically encumbered bis(oxazoline) ligand backbone, thus offering a de novo technology for accessing enantioenriched sp3-sp3 linkages via sp3 C-N functionalization. Our protocol is distinguished by its broad scope and generality across a wide number of counterparts, even in the context of late-stage functionalization. In addition, an enantioselective deaminative remote hydroalkylation reaction of unactivated internal olefins is within reach, thus providing a useful entry point for forging enantioenriched sp3-sp3 centers at remote sp3 C-H sites.

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