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BOC-D-Phenylalanine

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CAS:18942-49-9
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  • CAS:18942-49-9
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  • 2021-08-12
  • CAS:18942-49-9
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  • Purity: 99%+ HPLC
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BOC-D-Phenylalanine Basic information
Product Name:BOC-D-Phenylalanine
Synonyms:BOC-D-PHE;BOC-D-PHE-OH;BOC-D-PHENYLALANINE;(R)-2-TERT-BUTOXYCARBONYLAMINO-3-PHENYL-PROPIONIC ACID;N-T-BOC-D-PHENYLALANINE;N-(TERT-BUTOXYCARBONYL)-D-PHENYLALANINE;Boc-D-phenylalanine≥ 99% (HPLC);N-ALPHA-TERT-BUTYLOXYCARBONYL-D-PHENYLALANINE
CAS:18942-49-9
MF:C14H19NO4
MW:265.3
EINECS:606-177-6
Product Categories:Phenylalanine [Phe, F];Boc-Amino Acids and Derivative;Amino Acids (N-Protected);Biochemistry;Boc-Amino Acids;Boc-Amino acid series;Amino Acids
Mol File:18942-49-9.mol
BOC-D-Phenylalanine Structure
BOC-D-Phenylalanine Chemical Properties
Melting point 78-87 °C
alpha -26 º (c=2,ethanol)
Boiling point 408.52°C (rough estimate)
density 1.1356 (rough estimate)
refractive index -25 ° (C=1, EtOH)
storage temp. 2-8°C
solubility DMSO, Ethanol, Methanol
pka3.88±0.10(Predicted)
form Fine Crystalline Powder
color White
Optical Rotation[α]20/D 25±1°, c = 1% in ethanol
Water Solubility insoluble
BRN 3593396
Major Applicationpeptide synthesis
InChI1S/C14H19NO4/c1-14(2,3)19-13(18)15-11(12(16)17)9-10-7-5-4-6-8-10/h4-8,11H,9H2,1-3H3,(H,15,18)(H,16,17)/t11-/m1/s1
InChIKeyZYJPUMXJBDHSIF-LLVKDONJSA-N
SMILESCC(C)(C)OC(=O)N[C@H](Cc1ccccc1)C(O)=O
CAS DataBase Reference18942-49-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Safety Statements 24/25
WGK Germany 3
HS Code 29242990
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
BOC-D-Phenylalanine Usage And Synthesis
DescriptionBOC-D-Phenylalanine is the BOC (tert-butyloxycarbonyl) protected form of D-phenylalanine. It can be used in the synthesis of benzo[de][1,7] napthyridinones as PARP1 inhibitors. It is also an important reagent during the manufacturing of proline-containing, ß-turn mimetic cycle tetrapeptides.
Chemical Propertieswhite fine crystalline powder
UsesBoc-D-Phenylalanine is used in the synthesis of benzo[de][1,7]napthyridinones as PARP1 inhibitors. Also it is an important reagent in the preparation of proline-containing, β-turn mimetic cycle tetrapeptides.
reaction suitabilityreaction type: Boc solid-phase peptide synthesis
Referenceshttps://www.clearsynth.com/en/CST07663.html
http://www.biocompare.com/Protein-Biochemistry/10318-Boc-Protected-Phenylalanine-Monomers-and-Derivatives/
Tag:BOC-D-Phenylalanine(18942-49-9) Related Product Information
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