BOC-(R)-2-AMINO-3-(NAPHTHALEN-1-YL)PROPANOIC ACID

BOC-(R)-2-AMINO-3-(NAPHTHALEN-1-YL)PROPANOIC ACID - Names and Identifiers

Name	(R)-N-Boc-1-Naphthylalanine
Synonyms	Boc-D-1-Nal-OH BOC-D-ALA(1-NAPH)-OH Boc-D-1-Naphthylalanine BOC-3-(1-NAPHTHYL)-D-ALA (R)-N-Boc-1-Naphthylalanine BOC-3-(1-NAPHTHYL)-D-ALANINE Boc-3-(1-Naphthyl)-D-alanine Boc-D-3-(1-Naphthyl)-alanine BOC-BETA-(1-NAPHTHYL)-D-ALANINE N-ALPHA-T-BOC-BETA-(1-NAPHTHYL)-D-ALANINE N-ALPHA-T-BUTOXYCARBONYL-3-(1-NAPHTHYL)-D-ALANINE BOC-(R)-2-AMINO-3-(NAPHTHALEN-1-YL)PROPANOIC ACID N-ALPHA-(TERT-BUTYLOXYCARBONYL)-3-(1-NAPHTHYL)-D-ALANINE
CAS	76932-48-4
InChI	InChI=1/C18H21NO4/c1-18(2,3)23-17(22)19-15(16(20)21)11-13-9-6-8-12-7-4-5-10-14(12)13/h4-10,15H,11H2,1-3H3,(H,19,22)(H,20,21)/p-1/t15-/m1/s1

BOC-(R)-2-AMINO-3-(NAPHTHALEN-1-YL)PROPANOIC ACID - Physico-chemical Properties

Molecular Formula	C18H21NO4
Molar Mass	315.36
Density	1.2164 (rough estimate)
Melting Point	145-148°C(lit.)
Boling Point	454.92°C (rough estimate)
Specific Rotation(α)	53 º (c=2.5 in MeOH)
Flash Point	263.6°C
Vapor Presure	2.58E-11mmHg at 25°C
BRN	6180114
pKa	3.88±0.30(Predicted)
Storage Condition	Sealed in dry,2-8°C
Refractive Index	1.5740 (estimate)
MDL	MFCD00079668
Physical and Chemical Properties	alpha:53 o (c=2.5 in MeOH)

BOC-(R)-2-AMINO-3-(NAPHTHALEN-1-YL)PROPANOIC ACID - Risk and Safety

Hazard Symbols	Xi - Irritant
Safety Description	24/25 - Avoid contact with skin and eyes.
WGK Germany	3
HS Code	29242990
Hazard Class	IRRITANT

BOC-(R)-2-AMINO-3-(NAPHTHALEN-1-YL)PROPANOIC ACID - Introduction

(R)-N-Boc-1-Naphthylalanine((R)-N-Boc-1-Naphthylalanine) is an amino acid derivative with a variety of properties and uses.

Nature:
(R)-N-Boc-1-Naphthylalanine is a white crystalline powder with chemical stability and high solubility. It is a chiral molecule and exists only in the D-configuration. The compound is stable at room temperature.

Use:
(R)-N-Boc-1-Naphthylalanine is widely used in organic synthesis. It is often used as a substrate for enzymes or as a ligand for catalysts. In addition, it can also be used as a precursor compound containing amino acid protecting groups for the synthesis of polypeptides or other biologically active molecules.

Preparation Method:
The preparation of (R)-N-Boc-1-Naphthylalanine is generally accomplished by chemical synthesis. One common method is to react 1-naphthylalanine with a Boc protecting group to obtain the desired product. The specific synthesis path will be adjusted according to the specific experimental requirements and conditions.

Safety Information:
(R)-The N-Boc-1-Naphthylalanine is less dangerous when operated correctly. However, in any chemical experiment, safety procedures should be followed, including wearing appropriate personal protective equipment, avoiding direct contact with skin and eyes, paying attention to protective ventilation conditions, and avoiding inhalation or ingestion. At the same time, it must be stored in a dry, dark and sealed container to ensure the stability and safety of the compound. For more detailed safety information, refer to the compound's Safety Data Sheet (MSDS).

Last Update：2024-04-09 21:11:58