(S)-2-(TERT-BUTOXYCARBONYLAMINO)-3-(NAPHTHALEN-1-YL)PROPANOIC ACID - Names and Identifiers
Name | (S)-N-BOC-1-Naphthylalanine
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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
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CAS | 55447-00-2
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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 |
(S)-2-(TERT-BUTOXYCARBONYLAMINO)-3-(NAPHTHALEN-1-YL)PROPANOIC ACID - Physico-chemical Properties
Molecular Formula | C18H21NO4
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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 |
(S)-2-(TERT-BUTOXYCARBONYLAMINO)-3-(NAPHTHALEN-1-YL)PROPANOIC ACID - Risk and Safety
Hazard Symbols | Xi - Irritant
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Safety Description | S22 - Do not breathe dust.
S24/25 - Avoid contact with skin and eyes.
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WGK Germany | 3 |
HS Code | 29242990 |
Hazard Class | IRRITANT |
(S)-2-(TERT-BUTOXYCARBONYLAMINO)-3-(NAPHTHALEN-1-YL)PROPANOIC ACID - 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