Benzyl N-(2-aminobenzoyl)glycinate

Basic Information

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CAS Number

150374-97-3

Molecular Formula

C16H16N2O3

Molecular Weight

284.32 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Carboxylic Acids

Basic Chemical Raw Materials Organic Chemicals Esters

Basic Chemical Raw Materials Organic Chemicals Ethers

Basic Chemical Raw Materials Organic Chemicals Amines

Fine Chemicals Dyes and Pigments Organic Dyes

Fine Chemicals Surfactants Anionic Surfactants

Basic Physical Properties

SMILES

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c1ccc(cc1)COC(=O)CNC(=O)c2ccccc2N

InChI

InChI=1S/C16H16N2O3/c17-14-9-5-4-8-13(14)16(20)18-10-15(19)21-11-12-6-2-1-3-7-12/h1-9H,10-11,17H2,(H,18,20)

InChIKey

HOBJXAZBLCOYBE-UHFFFAOYSA-N

LogP

1.742

Topological Polar Surface Area

81.42 Å²

Hydrogen Bond Donor/Acceptor

3 / 5

Synonyms & References

English

Benzyl 2-(2-aminobenzamido)acetate
benzyl 2-[(2-aminobenzoyl)amino]acetate
N-(2-Aminobenzoyl)glycine benzyl ester
N-2-AMINOBENZOYL GLYCINE BENZYL ESTER
Glycine, N-(2-aminobenzoyl)-, phenylmethyl ester
N-(2-aminobenzoyl)glycine phenylmethyl ester

MDL Number

MFCD11553115

Customs Code

2924299090

FAQ

What are the physical and chemical properties of Benzyl N-(2-aminobenzoyl)glycinate (CAS: 150374-97-3)?

Benzyl N-(2-aminobenzoyl)glycinate is a white crystalline solid with a molecular weight of approximately 342.35 g/mol. It is slightly soluble in water and more soluble in organic solvents. The compound is stable under normal conditions but may react with strong acids or bases. It has a low reactivity in most cases but can undergo hydrolysis under basic conditions.

How is Benzyl N-(2-aminobenzoyl)glycinate (CAS: 150374-97-3) typically synthesized?

Benzyl N-(2-aminobenzoyl)glycinate is typically synthesized via a multi-step process involving the condensation of benzyl glycinate with 2-aminobenzoyl chloride. The synthesis often employs a catalytic amount of a strong base like triethylamine to improve yield and selectivity. The reaction is carried out at room temperature, and the product is isolated by recrystallization.

What industries use Benzyl N-(2-aminobenzoyl)glycinate (CAS: 150374-97-3)?

Benzyl N-(2-aminobenzoyl)glycinate is used in the pharmaceutical industry for the synthesis of certain medicinal compounds. It is also employed in the polymer industry as a potential monomer for producing specific polymers with unique properties. Additionally, it finds applications in the sensor and semiconductor industries due to its potential as a chelating agent.

What precautions should be taken when handling Benzyl N-(2-aminobenzoyl)glycinate (CAS: 150374-97-3)?

When handling Benzyl N-(2-aminobenzoyl)glycinate, it is important to wear appropriate personal protective equipment (PPE) such as gloves, goggles, and a lab coat. The material should be stored in a dry, cool place, away from strong acids and bases. Fume hoods should be used during the synthesis and handling of this compound to minimize inhalation risks. In case of a spill, it should be cleaned up immediately using appropriate spill kits, and the area should be well-ventilated. Always consult the Safety Data Sheet (SDS) for detailed handling and disposal information.