Boc-β-HoPhe(3-Me)-OH

Boc-β-HoPhe(3-Me)-OH - Names and Identifiers

Name	Boc-(S)-3-Amino-4-(3-methyl-phenyl)-butyric acid
Synonyms	Boc-β-HoPhe(3-Me)-OH BOC-L-Β-HOMOPHE(3-ME)-OH Boc-(S)-3-Amino-4-(3-methyl-phenyl)-butyric acid N-Boc-S-3-Amino-4-(3-methyl-phenyl)-butyric acid (S)-3-((tert-Butoxycarbonyl)amino)-4-(m-tolyl)butanoic acid (Tert-Butoxy)Carbonyl (S)-3-Amino-4-(3-methyl-phenyl)-butyric acid (S)-N-(tert-Butoxycarbonyl)-3-amino-4-(3-methylphenyl)butyric acid (3S)-3-{[(tert-butoxy)carbonyl]amino}-4-(3-methylphenyl)butanoic acid Boc-3-Methyl-L-β-hoMophenylalanine Boc-(S)-3-aMino-4-(3-Methylphenyl)butyric acid
CAS	270062-93-6

Boc-β-HoPhe(3-Me)-OH - Physico-chemical Properties

Molecular Formula	C16H23NO4
Molar Mass	293.36
Storage Condition	2-8°C

Boc-β-HoPhe(3-Me)-OH - Risk and Safety

Hazard Class

IRRITANT

Boc-β-HoPhe(3-Me)-OH - Introduction

Boc-(S)-3-Amino-4-(3-methyl-phenyl)-butyric is an organic compound with the chemical formula C16H23NO4.

In terms of properties, it is a colorless to light yellow solid, stable at room temperature. It is a water-insoluble compound and soluble in organic solvents such as methanol, ethanol and chloroform. Its melting point is about 80~90 ℃.

This compound has a wide range of applications in pharmaceutical chemistry and organic synthesis. It is often used as an intermediate in the synthesis of peptides and proteins. It can be used as a reagent to protect the carboxyl group of amino acids to prevent unnecessary reactions of the carboxyl group. In addition, it can also be used as a raw material for drugs, such as precursors for tumor treatment drugs.

In terms of preparation, a commonly used synthesis method is to generate Boc-(S)-3-methylbenzylaminobutyric anhydride by acyl chloride reaction of p-methylphenylimine and benzoic acid. This anhydride is then reacted with an appropriate amine to give the desired product Boc-(S)-3-Amino-4-(3-methyl-phenyl)-butyric acid.

When using and storing, you need to pay attention to safety matters. This compound may be irritating to the eyes, skin and respiratory system, so wear protective equipment. Avoid contact with strong oxidants and strong acids to avoid dangerous reactions. Should be stored in a dry, cool place, away from fire and combustibles. Good laboratory practices and measures should be taken to ensure safety when handling this compound.

Last Update：2024-04-10 22:30:50