BOC-(S)-3-AMINO-3-(4-FLUORO-PHENYL)-PROPIONIC ACID

BOC-(S)-3-AMINO-3-(4-FLUORO-PHENYL)-PROPIONIC ACID - Names and Identifiers

Name	Boc-L-3-Amino-3-(4-fluorophenyl)-propionic acid
Synonyms	RARECHEM LK TC T330 BOC-BETA-PHE(4-F)-OH BOC-D-PHG(4F)-(C*CH2)OH Boc-3-S-4-Fluorophenylalanine BOC-4-FLUORO-D-BETA-PHENYLALANINE BOC-(S)-4-FLUORO-BETA-PHENYLALANINE BOC PROTECTED (S)-B-(P-FLUOROPHENYL)-B-ALANINE Boc-L-3-Amino-3-(4-fluorophenyl)-propionic acid Boc-(S)-3-Amino-3-(4-fluorophenyl)-propionic acid BOC-(S)-3-AMINO-3-(4-FLUORO-PHENYL)-PROPIONIC ACID BOC-(S)-3-AMINO-3-(4-FLUORO-PHENYL)-PROPANOIC ACID
CAS	479064-88-5
InChI	InChI=1/C14H18FNO4/c1-14(2,3)20-13(19)16-11(8-12(17)18)9-4-6-10(15)7-5-9/h4-7,11H,8H2,1-3H3,(H,16,19)(H,17,18)/t11-/m0/s1

BOC-(S)-3-AMINO-3-(4-FLUORO-PHENYL)-PROPIONIC ACID - Physico-chemical Properties

Molecular Formula	C14H18FNO4
Molar Mass	283.3
Density	1.214±0.06 g/cm3(Predicted)
Melting Point	110-116 °C
Boling Point	424.5±40.0 °C(Predicted)
Flash Point	210.5°C
Vapor Presure	5.8E-08mmHg at 25°C
pKa	4.31±0.10(Predicted)
Storage Condition	Sealed in dry,Room Temperature
Refractive Index	1.516

BOC-(S)-3-AMINO-3-(4-FLUORO-PHENYL)-PROPIONIC ACID - Risk and Safety

WGK Germany

BOC-(S)-3-AMINO-3-(4-FLUORO-PHENYL)-PROPIONIC ACID - Introduction

Boc-L-3-Amino-3-(4-fluorophenyl)-propionic acid is an organic compound whose chemical formula is C15H19FNO4. It is a solid with a white or off-white color.

Boc-L-3-Amino-3-(4-fluorophenyl)-propionic acid is an amino acid derivative with important biochemical and pharmaceutical applications. It is a commonly used protecting group (Boc group) and pharmaceutical active ingredient in targeted drug delivery system. Its uses include the synthesis of peptides, proteins and drugs. It can also be used as a synthetic intermediate in pharmaceutical research and development for the preparation of molecules with specific biological activities.

The preparation method of Boc-L-3-Amino-3-(4-fluorophenyl)-propionic acid is generally realized by organic chemical synthesis. A common synthesis method is to react L-alanine with 4-fluorobenzoic anhydride under appropriate solvent conditions, and then undergo a protection reaction to finally obtain the target product.

Regarding safety information, it is a chemical that needs to be operated in a laboratory or professional environment. When using and handling, it is necessary to follow the general safety laboratory procedures and wear appropriate personal protective equipment, such as laboratory gloves, glasses and laboratory coats. In addition, direct contact with skin and eyes should be avoided, and inhalation of dust or gas should be avoided. In case of accidental contact or inhalation, please consult a professional doctor in time.

Last Update：2024-04-09 20:52:54