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BOC-L-PENTAFLUOROPHENYLALANINE is a chemical compound that serves as an intermediate in the synthesis of various peptides and coatings. It is characterized by the presence of a BOC (tert-butyloxycarbonyl) protecting group and a pentafluorophenylalanine moiety, which contribute to its unique properties and applications.

34702-60-8

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34702-60-8 Usage

Uses

Used in Pharmaceutical Industry:
BOC-L-PENTAFLUOROPHENYLALANINE is used as a building block for the synthesis of peptides with specific biological activities. Its unique structure allows for the creation of peptides that can be used as therapeutic agents or for research purposes.
Used in Coatings Industry:
BOC-L-PENTAFLUOROPHENYLALANINE is used as an intermediate in the self-assembly of tripeptides into functional coating materials. These coatings are designed to resist biofouling, which is the accumulation of microorganisms, algae, or other biological matter on surfaces. This property makes the coatings suitable for various applications, such as marine coatings for ships and underwater structures, medical device coatings to prevent bacterial adhesion, and industrial coatings for equipment exposed to harsh environments.

Check Digit Verification of cas no

The CAS Registry Mumber 34702-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,7,0 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 34702-60:
(7*3)+(6*4)+(5*7)+(4*0)+(3*2)+(2*6)+(1*0)=98
98 % 10 = 8
So 34702-60-8 is a valid CAS Registry Number.

34702-60-8 Well-known Company Product Price

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  • Aldrich

  • (670138)  Boc-pentafluoro-L-phenylalanine  ≥98.0% (HPLC)

  • 34702-60-8

  • 670138-1G

  • 1,584.18CNY

  • Detail

34702-60-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-(2,3,4,5,6-pentafluorophenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names BOC-PENTAFLUORO-PHE-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:34702-60-8 SDS

34702-60-8Upstream product

34702-60-8Downstream Products

34702-60-8Relevant academic research and scientific papers

Incorporation of fluorinated phenylalanine generates highly specific inhibitor of proteasome's chymotrypsin-like sites

Geurink, Paul P.,Liu, Nora,Spaans, Michiel P.,Downey, Sondra L.,Van Den Nieuwendijk, Adrianus M. C. H.,Van Der Marel, Gijsbert A.,Kisselev, Alexei F.,Florea, Bogdan I.,Overkleeft, Herman S.

supporting information; experimental part, p. 2319 - 2323 (2010/08/06)

Proteasomal processing is conducted by three individual catalytic subunits, namely β11, β2, and β5. Subunit-specific inhibitors are useful tools in dissecting the role of these individual subunits and are leads toward the development of antitumor agents. We here report that the presence of fluorinated phenylalanine derivatives in peptide based proteasome inhibitors has a profound effect on inhibitor potency and selectivity. Specifically, compound 4a emerges as one of the most β5 specific inhibitors known to date.

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