DL-N-Boc-β-(2-Chlorophenyl)-alanine

DL-N-Boc-β-(2-Chlorophenyl)-alanine - Names and Identifiers

Name	3-[(tert-butoxycarbonyl)amino]-3-(2-chlorophenyl)propanoic acid
Synonyms	Boc-D-b-Phe(2-Cl)-OH FMoc-2-Chloro-D-b-phenylalanine DL-N-Boc-β-(2-Chlorophenyl)-alanine (R)-N-Boc-2-Chloro-Beta-Phenylalanine (R)-N-BOC-2-CHLORO-BETA-PHENYLALANINE Boc-D-3-Amino-3-(2-chloro)propanoic acid Boc-(S)-3-Amino-3-(2-chlorophenyl)-propionic acid Boc-(R)-3-Amino-3-(2-chlorophenyl)-propionic acid 3-[(tert-butoxycarbonyl)amino]-3-(2-chlorophenyl)propanoic acid (R)-3-((tert-butoxycarbonyl)amino)-3-(2-chlorophenyl)propanoic acid (Tert-Butoxy)Carbonyl (R)-3-Amino-3-(2-chloro-phenyl)propionic acid (3R)-3-{[(tert-butoxy)carbonyl]amino}-3-(2-chlorophenyl)propanoic acid Benzenepropanoic acid, 2-chloro-β-[[(1,1-dimethylethoxy)carbonyl]amino]-, (βR)-
CAS	500789-05-9 284493-66-9 500770-73-0
InChI	InChI=1/C14H18ClNO4/c1-14(2,3)20-13(19)16-11(8-12(17)18)9-6-4-5-7-10(9)15/h4-7,11H,8H2,1-3H3,(H,16,19)(H,17,18)

DL-N-Boc-β-(2-Chlorophenyl)-alanine - Physico-chemical Properties

Molecular Formula	C14H18ClNO4
Molar Mass	299.75
Density	1.243g/cm³
Boling Point	446.9°C at 760 mmHg
Flash Point	224.1°C
Vapor Presure	9.06E-09mmHg at 25°C
Storage Condition	2-8°C
Refractive Index	1.538

DL-N-Boc-β-(2-Chlorophenyl)-alanine - Introduction

3-[(tert-butoxycarbonyl)amino]-3-(2-chroophenyl) propanoic acid is a compound, its structural formula is: N-Boc-L-phenylalanine, chemical name is 3-[(tert-butoxycarbonyl)amino]-3-(2-chroophenyl) propanoic acid.

Nature:
-Appearance: solid, the color can be white or similar to white crystalline powder.
-Melting point: about 105-108°C.
-Detailed information on physical and chemical properties can be found in laboratory manuals or synthesis literature, as specific synthesis methods may vary slightly.

Use:
- 3-[(tert-butoxycarbonyl)amino]-3-(2-chroophenyl) propanoic acid is a commonly used amino acid derivative, which is widely used in drug synthesis and research fields. It can be used as a chiral starting material for the synthesis of chiral drugs and bioactive molecules.
-In organic synthesis, it is often used as chiral reagents, catalysts and ligands for catalytic reactions and the synthesis of chiral molecules.

Preparation Method:
-A commonly used preparation method is obtained by the condensation reaction of o-chlorophenacetyl chloride (2-chlorophenylacetyl chloride) and N-Boc (N-Boc-methylamine).
-The specific synthesis method is complex and varies with specific synthesis objectives and conditions. It is recommended to make specific inquiries and references in the organic synthesis laboratory or literature.

Safety Information:
- 3-[(tert-butoxycarbonyl)amino]-3-(2-chlorophenyl)propanoic acid safety information can be obtained from its related substance safety data sheet (MSDS).
-When operating, follow the general laboratory safety practices and use personal protective equipment.
-During handling, storage and handling, care should be taken to prevent contact with skin, inhalation or ingestion, and to avoid contact with strong oxidants, strong acids and other substances.
-If there are special circumstances or specific requirements, please consult the relevant professionals or refer to the specific safety operation manual.

Last Update：2024-04-09 19:05:49