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2-amino-5-phenylpentanoic acid, also known as phenylglycine, is an organic compound with the chemical formula C11H15NO2. It is an alpha-amino acid, which means it contains an amino group and a carboxylic acid group on the first carbon atom of the molecule. As a chiral compound, it has two enantiomers that are mirror images of each other. This synthetic compound is not naturally occurring in the human body but is widely used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and peptide-based drugs.

34993-02-7

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34993-02-7 Usage

Uses

Used in Pharmaceutical Industry:
2-amino-5-phenylpentanoic acid is used as a key building block for the synthesis of various pharmaceuticals, including antibiotics, anti-inflammatory drugs, and other therapeutic agents. Its unique structure allows for the creation of chiral centers, which are crucial for the development of enantiomer-specific drugs with improved efficacy and reduced side effects.
Used in Agrochemical Industry:
In the agrochemical industry, 2-amino-5-phenylpentanoic acid is used as a precursor in the synthesis of various agrochemicals, such as herbicides and pesticides. Its incorporation into these compounds can enhance their selectivity and effectiveness in controlling pests and weeds, while minimizing the impact on non-target organisms and the environment.
Used in Peptide-based Drug Production:
2-amino-5-phenylpentanoic acid is utilized as a building block in the production of peptide-based drugs. Its incorporation into peptide sequences can impart specific biological activities, such as antimicrobial, antiviral, or anticancer properties. The chiral nature of 2-amino-5-phenylpentanoic acid also allows for the development of enantiomer-specific peptide drugs with improved pharmacokinetics and reduced side effects.
Used in Laboratory Research:
2-amino-5-phenylpentanoic acid is employed in laboratory research for the study of protein synthesis, enzyme mechanisms, and the development of novel synthetic routes. Its chiral properties make it an ideal candidate for investigating the role of stereochemistry in biological systems and the design of enantioselective catalysts and reagents.

Check Digit Verification of cas no

The CAS Registry Mumber 34993-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,9,9 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 34993-02:
(7*3)+(6*4)+(5*9)+(4*9)+(3*3)+(2*0)+(1*2)=137
137 % 10 = 7
So 34993-02-7 is a valid CAS Registry Number.

34993-02-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-5-phenylpentanoic acid

1.2 Other means of identification

Product number -
Other names S-benzyl-L-cystein

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:34993-02-7 SDS

34993-02-7Relevant academic research and scientific papers

Synthesis method of multi-configuration long-chain phenyl amino acid compound

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, (2021/03/05)

The invention relates to a method for synthesizing a multi-configuration long-chain phenyl amino acid compound. The method comprises the following steps: reacting a compound shown in a formula I witha compound shown in a formula II or an isomer thereof in

Tricyclic erythromycin derivatives

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, (2008/06/13)

Compounds, or pharmaceutically acceptable salts and esters thereof, of the formula: wherein A, B, D and E, R1, R2, and Z are specifically defined, having antibacterial activity, pharmaceutical compositions containing said compounds, treatment of bacterial infections with such compositions, and processes for the preparation of the compounds.

SULFONAMIDE INHIBITORS OF MATRIX METALLOPROTEINASES

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, (2008/06/13)

Sulfonamide compounds are described which are inhibitors of matrix metalloproteinases, particularly stromelysin-1 and gelatinase A (72 kD gelatinase). Also described are methods for the treatment of multiple sclerosis, atherosclerotic plaque rupture, aortic aneurism, heart failure, restenosis, periodontal disease, corneal ulceration, burns, decubital ulcers, chronic ulcers or wounds, cancer metastasis, tumor angiogenesis, arthritis, or other autoimmune or inflammatory disorders dependent upon tissue invasion by leukocytes using the compounds.

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