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3-(4-Acetyl-phenyl)-2-amino-propionic acid hydrochloride, a chemical compound with the molecular formula C11H14ClNO3, is a derivative of phenylalanine, an essential amino acid. It is characterized by its potential pharmaceutical applications due to its ability to inhibit enzymes involved in inflammation and pain pathways, as well as its potential antidepressant and anti-anxiety properties. The hydrochloride salt form of the compound enhances its stability and suitability for medical use, making it a promising candidate for the development of new medications for various health conditions.

22888-49-9

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22888-49-9 Usage

Uses

Used in Pharmaceutical Industry:
3-(4-Acetyl-phenyl)-2-amino-propionic acid hydrochloride is used as a building block for peptides and proteins, contributing to the development of new medications for various health conditions. Its ability to inhibit enzymes involved in inflammation and pain pathways makes it a valuable component in the creation of drugs targeting these areas.
Used in Anti-inflammatory and Pain Management Applications:
3-(4-Acetyl-phenyl)-2-amino-propionic acid hydrochloride is employed as an active pharmaceutical ingredient for the development of anti-inflammatory and pain management medications. Its enzyme-inhibiting properties allow it to effectively address inflammation and pain, providing relief to patients suffering from various conditions.
Used in Antidepressant and Anti-anxiety Medications:
3-(4-Acetyl-phenyl)-2-amino-propionic acid hydrochloride is utilized as a key component in the formulation of antidepressant and anti-anxiety medications. Its potential to modulate neurotransmitters and influence mood regulation makes it a promising candidate for the treatment of mental health disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 22888-49-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,8 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22888-49:
(7*2)+(6*2)+(5*8)+(4*8)+(3*8)+(2*4)+(1*9)=139
139 % 10 = 9
So 22888-49-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO3/c1-7(13)9-4-2-8(3-5-9)6-10(12)11(14)15/h2-5,10H,6,12H2,1H3,(H,14,15)

22888-49-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name DL-3-(p-acetylphenyl)-alanine

1.2 Other means of identification

Product number -
Other names para-acetylphenylalanine

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:22888-49-9 SDS

22888-49-9Relevant academic research and scientific papers

Diverse organo-peptide macrocycles via a fast and catalyst-free oxime/intein-mediated dual ligation

Satyanarayana, Maragani,Vitali, Francesca,Frost, John R.,Fasan, Rudi

, p. 1461 - 1463 (2012/03/26)

Macrocyclic Organo-Peptide Hybrids (MOrPHs) can be prepared from genetically encoded polypeptides via a chemoselective and catalyst-free reaction between a trifunctional oxyamino/amino-thiol synthetic precursor and an intein-fusion protein incorporating a bioorthogonal keto group.

Microwave-assisted synthesis of unnatural amino acids

Young, Douglas D.,Torres-Kolbus, Jessica,Deiters, Alexander

experimental part, p. 5478 - 5480 (2009/05/30)

Microwave irradiation has been proven to be a useful tool in the rapid assembly of racemic unnatural amino acids in only two steps. Additional benefits of this methodology are the commercial availability of the inexpensive starting materials and the high yields and high purities of the final amino acid products.

Protein arrays

-

, (2008/06/13)

The invention provides proteins attached to solid supports, and methods of preparing such solid support-bound proteins are provided. The proteins are attached to solid supports by means of an unnatural amino acid incorporated into the protein, which unnat

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