(S)-2-(tert-butoxycarbonylamino)-3-(4-chlorophenyl)propanoic acid - Names and Identifiers
(S)-2-(tert-butoxycarbonylamino)-3-(4-chlorophenyl)propanoic acid - Physico-chemical Properties
Molecular Formula | C14H18ClNO4
|
Molar Mass | 299.75 |
Density | 1.2167 (rough estimate) |
Melting Point | ~110°C |
Boling Point | 452.5±40.0 °C(Predicted) |
Specific Rotation(α) | 24 º (c=1,EtOH) |
BRN | 4261946 |
pKa | 3.83±0.10(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.6800 (estimate) |
MDL | MFCD00057808 |
Physical and Chemical Properties | Melting Point: 108°C |
(S)-2-(tert-butoxycarbonylamino)-3-(4-chlorophenyl)propanoic acid - 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 |
(S)-2-(tert-butoxycarbonylamino)-3-(4-chlorophenyl)propanoic acid - Introduction
(S)-N-BOC-4-Chlorophenylalanine, also known as (S)-N-BOC-4-Chlorophenylalanine, is an amino acid derivative.
Nature:
(S)-N-BOC-4-Chlorophenylalanine is a white crystalline powder, sometimes appear light yellow phenomenon. Its molecular formula is C14H17ClNO4 and its molecular weight is 293.74. It has one chiral center and is in the (S) configuration. In its chemical structure, a phenyl group is attached to a methyl group and a carboxyl group, and an amino group is attached to a chiral carbon.
Use:
(S)-N-BOC-4-Chlorophenylalanine are commonly used raw materials in the field of organic synthesis. It is often used in peptide synthesis and drug development as a chiral intermediate and protecting group. Because it has a protecting group (Boc group) and a chiral amino acid group, it can be used to control the reactivity and chiral selectivity of amino acids.
Preparation Method:
The preparation method of (S)-N-BOC-4-Chlorophenylalanine is relatively cumbersome and is usually achieved through multi-step synthesis. A common synthesis method is based on 4-chlorobenzaldehyde as raw material, through the addition of amino reaction, reduction, protection group and other steps of synthesis.
Safety Information:
(S)-N-BOC-4-Chlorophenylalanine has low toxicity under routine use conditions, it may still cause allergic reactions in sensitive people. In handling, care should be taken to avoid contact with the skin, inhalation and ingestion. Wear appropriate personal protective equipment, such as lab gloves and goggles, when used in a laboratory environment.
Last Update:2024-04-09 21:04:16