Boc-3-Methyl-L-phenylalanine Boc-M-Me-Phe-OH - Names and Identifiers
Name | BOC-L-3-Methylphe
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Synonyms | BOC-L-3-Methylphe Boc-L-3-Me-Phe-OH BOC-L-3-METHYL-PHE-OH Boc-L-3-Methylphenylalanine Boc-3-Methyl-L-phenylalanine Boc-3-Methyl-L-phenylalanine Boc-M-Me-Phe-OH Boc-L-3-Me-Phe-OH Boc-3-Methy-L-Phenylalanine (S)-2-Boc-2-amino-3-(3-methylphenyl)propionic acid L-Phenylalanine,N-[(1,1-diMethylethoxy)carbonyl]-3-Methyl-
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CAS | 114873-06-2
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InChI | InChI=1/C15H21NO4/c1-10-6-5-7-11(8-10)9-12(13(17)18)16-14(19)20-15(2,3)4/h5-8,12H,9H2,1-4H3,(H,16,19)(H,17,18)/t12-/m1/s1 |
Boc-3-Methyl-L-phenylalanine Boc-M-Me-Phe-OH - Physico-chemical Properties
Molecular Formula | C15H21NO4
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Molar Mass | 279.33 |
Density | 1.140±0.06 g/cm3(Predicted) |
Melting Point | 70°C |
Boling Point | 439.9±40.0 °C(Predicted) |
Specific Rotation(α) | 125 º (c=1,MeOH) |
Flash Point | 219.9°C |
Vapor Presure | 1.62E-08mmHg at 25°C |
Appearance | White powder |
BRN | 8989098 |
pKa | 3.92±0.10(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.526 |
MDL | MFCD01862944 |
Physical and Chemical Properties | Melting point 70°C specific rotation 125 ° (c = 1,MeOH)
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Boc-3-Methyl-L-phenylalanine Boc-M-Me-Phe-OH - Risk and Safety
Hazard Symbols | Xi - Irritant
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WGK Germany | 3 |
Hazard Class | IRRITANT |
Boc-3-Methyl-L-phenylalanine Boc-M-Me-Phe-OH - Introduction
BOC-L-3-Methylphenylalanine is a chemical with the following chemical properties and uses:
Nature:
BOC-L-3-Methylphenylalanine is a white crystalline solid with the formula C14H21NO4. Its molecular weight is 279.32g/mol. It is a non-natural amino acid derivative with chirality, specifically L-form. The compound is stable and does not decompose relatively easily.
Use:
BOC-L-3-Methylphenylalanine is commonly used as a reaction intermediate and reagent in organic synthesis. It is widely used in the synthesis of peptides, proteins and other biologically active molecules. BOC-L-3-methylphenylalanine can be used to construct polypeptide chains or modify proteins to study their structure and function.
Method:
The method for preparing BOC-L-3-methylphenylalanine generally includes the following steps: First, the BOC-protected L-3-methylphenylalanine is synthesized; then, the protecting group is removed by a base-promoted reaction, such as aminolysis or base hydrolysis, to obtain BOC-L-3-methylphenylalanine.
Safety Information:
BOC-L-3-Methylphenylalanine is highly safe, but as a chemical, it still needs to be properly handled and stored. When using, should follow the relevant safety procedures, such as wearing appropriate personal protective equipment (such as gloves, glasses).
Important Note: For detailed properties, uses, methods and safety information of chemicals, it is recommended to consult relevant and reliable chemical literature or consult professional laboratory personnel before laboratory operation.
Last Update:2024-04-10 22:29:15