Boc-pentafluoro-D-Phe-OH

Boc-pentafluoro-D-Phe-OH - Names and Identifiers

Name	Boc-pentafluoro-D-Phe-OH
Synonyms	Boc-D-Phe(5F)-OH RARECHEM BK PT 0107 Boc-pentafluoro-D-Phe-OH Boc-D-Pentafluorophenylalanine Boc-pentafluoro-D-phenylalanine Boc-3-(Pentafluorophenyl)-D-alanine (Tert-Butoxy)Carbonyl D-Pentafluorophe N-ALPHA-T-BUTOXYCARBONYL-D-PENTAFLUOROPHENYLALANINE (R)-Boc-2-amino-3-(pentafluorophenyl)propionic acid N-ALPHA-TERT-BUTYLOXYCARBONYL-D-PENTAFLUOROPHENYLALANINE (R)-2-TERT-BUTOXYCARBONYLAMINO-3-PENTAFLUOROPHENYL-PROPIONIC ACID
CAS	136207-26-6
InChI	InChI=1/C14H14F5NO4/c1-14(2,3)24-13(23)20-6(12(21)22)4-5-7(15)9(17)11(19)10(18)8(5)16/h6H,4H2,1-3H3,(H,20,23)(H,21,22)/t6-/m0/s1

Boc-pentafluoro-D-Phe-OH - Physico-chemical Properties

Molecular Formula	C14H14F5NO4
Molar Mass	355.26
Density	1.422±0.06 g/cm3(Predicted)
Boling Point	411.1±45.0 °C(Predicted)
Flash Point	202.4°C
Vapor Presure	1.7E-07mmHg at 25°C
pKa	3.70±0.20(Predicted)
Storage Condition	Sealed in dry,Store in freezer, under -20°C
Refractive Index	1.476

Boc-pentafluoro-D-Phe-OH - Risk and Safety

Hazard Symbols	Xi - Irritant
WGK Germany	3
Hazard Note	Harmful/Irritant/Keep Cold

Boc-pentafluoro-D-Phe-OH - Introduction

N-tert-butoxycarbonyl-D-pentafluorophenylalanine is an organic compound with the chemical formula C13H16F5NO4. It is a solid with a white to yellowish crystal form. It is a kind of amino acid derivatives, which plays an important role in biochemical research by changing the structure and function.

N-tert-Butoxycarbonyl-D-pentafluorophenylalanine is widely used in drug synthesis and biochemical research. It can be used as a substrate for the preparation of peptide drugs, protein engineering and enzyme-catalyzed reactions. It can also be used for chemical reactions such as drug crosslinking and modification.

The method for preparing N-tert-butoxycarbonyl-D-pentafluorophenylalanine generally involves the following steps: firstly, pentafluorobenzoyl chloride is selected as a starting material, and the target product is finally obtained by esterification reaction with N-tert-butoxycarbonyl-L-phenylalanine. The specific experimental conditions and procedures can be adjusted according to the reaction requirements.

N-tert-butoxycarbonyl-D-pentafluorophenylalanine should comply with certain safety precautions when used. It is an organic compound that may cause irritation to the eyes, skin and respiratory tract. Therefore, appropriate protective equipment, such as laboratory gloves and protective glasses, should be worn during the operation, and a well-ventilated laboratory environment should be maintained. At the same time, the compound should be stored properly to avoid contact with flammable and oxidizing substances to prevent fire and explosion hazards.

Last Update：2024-04-09 21:11:58