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136207-26-6

BOC-D-PENTAFLUOROPHENYLALANINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • D-Phenylalanine,N-[(1,1-dimethylethoxy)carbonyl]-2,3,4,5,6-pentafluoro-

    Cas No: 136207-26-6

  • USD $ 1.9-2.9 / Gram

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  • 136207-26-6 Structure

  • Basic information

    1. Product Name: BOC-D-PENTAFLUOROPHENYLALANINE
    2. Synonyms: D-PENTAFLUOROPHENYLALANINE, BOC PROTECTED;BOC-D-PHE(F5)-OH;BOC-D-PENTAFLUOROPHE;BOC-D-PENTAFLUOROPHENYLALANINE;BOC-1,2,3,4,5-PENTAFLUORO-D-PHENYLALANINE;BOC-PENTAFLUORO-D-PHENYLALANINE;BOC-PENTAFLUORO-D-PHE-OH;RARECHEM BK PT 0107
    3. CAS NO:136207-26-6
    4. Molecular Formula: C14H14F5NO4
    5. Molecular Weight: 355.26
    6. EINECS: N/A
    7. Product Categories: Amino Acids;Phenylalanine analogs and other aromatic alpha amino acids;a-amino
    8. Mol File: 136207-26-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 411.1 °C at 760 mmHg
    3. Flash Point: 202.4 °C
    4. Appearance: /
    5. Density: 1.422 g/cm3
    6. Vapor Pressure: 1.7E-07mmHg at 25°C
    7. Refractive Index: 1.476
    8. Storage Temp.: -15°C
    9. Solubility: N/A
    10. PKA: 3.70±0.20(Predicted)
    11. CAS DataBase Reference: BOC-D-PENTAFLUOROPHENYLALANINE(CAS DataBase Reference)
    12. NIST Chemistry Reference: BOC-D-PENTAFLUOROPHENYLALANINE(136207-26-6)
    13. EPA Substance Registry System: BOC-D-PENTAFLUOROPHENYLALANINE(136207-26-6)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 136207-26-6(Hazardous Substances Data)

136207-26-6 Usage

Uses

BOC-D-Pentafluorophenylalanine, is a Phenylalanine derivative, used in peptide chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 136207-26-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,2,0 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136207-26:
(8*1)+(7*3)+(6*6)+(5*2)+(4*0)+(3*7)+(2*2)+(1*6)=106
106 % 10 = 6
So 136207-26-6 is a valid CAS Registry Number.
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

136207-26-6 Well-known Company Product Price

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  • Aldrich

  • (670235)  Boc-pentafluoro-D-phenylalanine  ≥98.0% (HPLC)

  • 136207-26-6

  • 670235-1G

  • 1,722.24CNY

  • Detail

136207-26-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name BOC-D-Pentafluorophenylalanine

1.2 Other means of identification

Product number -
Other names (R)-2-(Boc-amino)-3-(pentafluorophenyl)propionic acid

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:136207-26-6 SDS

136207-26-6Upstream product

136207-26-6Relevant articles and documents

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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