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Boc-2,4-Difluoro-L-Phenylalanine is an organic compound with the chemical formula C16H19F2NO4. It is a protected amino acid that plays a significant role in the synthesis of peptides and proteins. The Boc (tert-butyloxycarbonyl) protective group shields the amino acid, preventing premature reactions during peptide assembly. The 2,4-difluoro substitution on the phenylalanine residue makes it a valuable tool in chemical and pharmaceutical research, providing insights into the effects of fluorine substitution on biochemical processes.

167993-00-2

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167993-00-2 Usage

Uses

Used in Chemical Research:
Boc-2,4-Difluoro-L-Phenylalanine is used as a research compound for studying the influence of fluorine substitution on biochemical processes. Its unique structure allows researchers to investigate the impact of fluorination on the properties and reactivity of amino acids and peptides.
Used in Pharmaceutical Research:
Boc-2,4-Difluoro-L-Phenylalanine is used as a building block in the synthesis of novel peptides and proteins with potential pharmaceutical applications. The 2,4-difluoro substitution may impart altered biological activity or improved pharmacokinetic properties to the resulting molecules, making them valuable for drug discovery and development.
Used in Peptide Synthesis:
Boc-2,4-Difluoro-L-Phenylalanine is used as a protected amino acid in the synthesis of peptides. The Boc group protects the amino acid from premature reactions during the assembly process, ensuring the correct formation of peptide bonds and the desired peptide sequence.
Used in Protein Engineering:
Boc-2,4-Difluoro-L-Phenylalanine is used as a component in the engineering of proteins with altered properties. The incorporation of this amino acid into protein structures can lead to changes in protein folding, stability, or function, which may be exploited for various biotechnological or therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 167993-00-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,9,9 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 167993-00:
(8*1)+(7*6)+(6*7)+(5*9)+(4*9)+(3*3)+(2*0)+(1*0)=182
182 % 10 = 2
So 167993-00-2 is a valid CAS Registry Number.

167993-00-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-3-(2,4-difluorophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid

1.2 Other means of identification

Product number -
Other names BOC-PHE(2,4-F2)-OH

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:167993-00-2 SDS

167993-00-2Downstream Products

167993-00-2Relevant academic research and scientific papers

Synthesis of a complete set of L-difluorophenylalanines, L-(F2)Phe, as molecular explorers for the CH/π interaction between peptide ligand and receptor

Fujita, Tsugumi,Nose, Takeru,Matsushima, Ayami,Okada, Kazushi,Asai, Daisuke,Yamauchi, Yasuko,Shirasu, Naoto,Honda, Takeshi,Shigehiro, Daiki,Shimohigashi, Yasuyuki

, p. 923 - 927 (2007/10/03)

A complete set of difluorophenylalanines in the L-configuration [L- (F2)Phe] (namely, L-(2,3-F2)Phe, L-(2,4-F2)Phe, L-(2,5-F2)Phe, L-(2,6- F2)Phe, L-(3,4-F2)Phe, L-(3,5-F2)Phe) w

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