Boc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric acid

Boc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric acid - Names and Identifiers

Name	Boc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric acid
Synonyms	RARECHEM AK PT B055 BOC-BETA-HOPHE(4-ME)-OH BOC-PHE(4-ME)-(C*CH2)OH BOC-4-METHYL-L-BETA-HOMOPHENYLALANINE BOC-(S)-3-AMINO-4-(4-METHYLPHENYL)BUTANOIC ACID BOC-(S)-3-AMINO-4-(4-METHYL-PHENYL)-BUTYRIC ACID Boc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric acid N-BETA-T-BUTOXYCARBONYL-L-HOMO(4-METHYLPHENYL)ALANINE N-T-BUTOXYCARBONYL-(S)-3-AMINO-4-(4-METHYLPHENYL)BUTANOIC ACID
CAS	270062-96-9

Boc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric acid - Physico-chemical Properties

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

Boc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric acid - Risk and Safety

Safety Description	S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes.
WGK Germany	3
FLUKA BRAND F CODES	10
Hazard Class	IRRITANT

Boc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric acid - Introduction

Boc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric is an organic compound whose chemical formula is C16H23NO4. The following is a description of some of its properties, uses, methods and safety information:

Nature:
1. Appearance: usually white crystalline solid;
2. melting point: about 120-125 degrees Celsius;
3. Stability: Stable at room temperature, soluble in some organic solvents, such as dimethyl sulfoxide (DMSO), dichloromethane, etc;
4. optical activity: Boc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric acid has chirality, where (S) indicates that it is a levorotatory isomer.

Use:
Boc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric acid is commonly used in the field of organic synthesis as an intermediate for the preparation of chiral compounds. It is a common amino acid protecting group, by adding it to the molecule, the amino acid can be kept stable during the synthesis process.

Preparation Method:
The preparation of Boc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric acid usually includes the following steps:
1. First, 3-amino -4-(4-methylphenyl) butyric acid was synthesized by chemical reaction;
2. Then, it reacts with Boc(tert-butoxycarbonyl) group to generate Boc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric acid.

Safety Information:
1. Boc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric acid is not a hazardous chemical, but it still needs to comply with the basic laboratory safety operation specifications;
2. In the process of use, avoid contact with strong oxidants, strong acids and other harmful substances to avoid dangerous reactions;
3. May be irritating to the eyes, skin and respiratory tract, so wear appropriate personal protective equipment when using.

Last Update：2024-04-10 22:29:15