3-Naphth-1-yl-L-alanine, N-BOC protected

3-Naphth-1-yl-L-alanine, N-BOC protected - Names and Identifiers

Name	(S)-N-BOC-1-Naphthylalanine
Synonyms	Boc-1-Nal-OH Boc-L-1-Naphthylalanine (S)-N-BOC-1-Naphthylalanine Boc-3-(1-Naphthyl)-L-alanine Boc-L-3-(1-Naphthyl)-alanine 3-(NAPHTHALEN-1-YL)-N-BOC-L-ALANINE O 3-Naphth-1-yl-L-alanine, N-BOC protected (S)-2-TERT-BUTOXYCARBONYLAMINO-3-NAPHTHALEN-1-YL-PROPIONIC ACID 1-Naphthalenepropanoicacid, a-[[(1,1-diMethylethoxy)carbonyl]aMi (S)-2-(TERT-BUTOXYCARBONYLAMINO)-3-(NAPHTHALEN-1-YL)PROPANOIC ACID
CAS	55447-00-2
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)/t15-/m0/s1

3-Naphth-1-yl-L-alanine, N-BOC protected - Physico-chemical Properties

Molecular Formula	C18H21NO4
Molar Mass	315.36
Density	1.2164 (rough estimate)
Boling Point	454.92°C (rough estimate)
Flash Point	263.6°C
Vapor Presure	2.58E-11mmHg at 25°C
pKa	3.88±0.30(Predicted)
Storage Condition	Keep in dark place,Sealed in dry,2-8°C
Refractive Index	1.5740 (estimate)
MDL	MFCD00085377

3-Naphth-1-yl-L-alanine, N-BOC protected - Risk and Safety

Hazard Symbols	Xi - Irritant
Safety Description	S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes.
WGK Germany	3
HS Code	29242990
Hazard Class	IRRITANT

3-Naphth-1-yl-L-alanine, N-BOC protected - Introduction

(S)-N-BOC-1-Naphthylalanine, also known as (S)-N-BOC-1-Naphthylalanine, is an amino acid derivative. It contains the structure of the natural amino acid alanine, with a 1-naphthyl group attached to the alpha position of the alanine. It is usually in the form of a white solid.

(S)-N-BOC-1-Naphthylalanine are mainly used as reagents in organic synthesis to synthesize compounds with specific structures and functions. It can be used to synthesize polypeptides, drug molecules and other biologically active molecules. Because of its special structure, specific drug molecular skeleton or functional groups can be introduced through it.

Methods for preparing (S)-N-BOC-1-Naphthylalanine are generally chemical synthesis by protecting groups of amino acids. The general procedure involves reacting alanine with 1-naphthoyl chloride and then with a Boc (n-butoxycarbonyl) group to introduce a protecting group.

Regarding safety information,(S)-N-BOC-1-Naphthylalanine are generally relatively safe under correct handling and storage conditions. However, it may cause irritation to the eyes, skin and respiratory system. When in use, wear appropriate protective equipment to avoid direct contact. In addition, it should be stored in a dry, cool place, and avoid contact with oxidants and high temperature conditions to prevent its decomposition or dangerous reactions.

Please note that the information provided above is for informational purposes only. When using (S)-N-BOC-1-Naphthylalanine, please follow the standard operating procedures of the chemical laboratory and operate according to specific experimental requirements and safety guidelines.

Last Update：2024-04-09 20:45:29