D-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-2,3,4,5,6-pentafluoro-|136207-26-6,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-

O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]

Tris(dibenzylideneacetone)dipalladium

C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C

Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

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

OC(=O)[C@@H](Cc1c(F)c(F)c(c(c1F)F)F)NC(=O)OC(C)(C)C

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Chemical Name:	D-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-2,3,4,5,6-pentafluoro-
CAS Number:	136207-26-6
Product Number:	AG003C8G(AGN-PC-0O19JU)
Synonyms:
MDL No:
Molecular Formula:	C14H14F5NO4
Molecular Weight:	355.2573

Identification/Properties
Safety Information
NMR Spectrum
Other Analytical Data
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Identification/Properties

Properties

Storage:

Keep in dry area;-10 ℃;

Form:

Solid

Computed Properties

Molecular Weight:

355.261g/mol

XLogP3:

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

355.084g/mol

Monoisotopic Mass:

355.084g/mol

Topological Polar Surface Area:

75.6A^2

Heavy Atom Count:

Formal Charge:

Complexity:

457

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

Signal Word:

Warning

UN#:

Hazard Statements:

H302-H315-H319-H335

Precautionary Statements:

P261-P280-P301+P312-P302+P352-P305+P351+P338

Class:

Packing Group:

NMR Spectrum

Other Analytical Data

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Chemical Structure

The (R)-2-((tert-butoxycarbonyl)amino)-3-(perfluorophenyl)propanoic acid, commonly known as $name$, is a valuable compound widely used in chemical synthesis processes. Its unique structure and properties make it an essential reagent in various synthetic reactions. One of the primary applications of $name$ in chemical synthesis is as a chiral auxiliary. This compound can be utilized to introduce chirality into molecules, enabling the selective formation of enantiomerically pure products. By leveraging the (R)-configuration of the amino and propanoic acid groups in $name$, chemists can control the stereochemistry of reactions and obtain optically pure compounds.Additionally, $name$ serves as a versatile building block in the synthesis of complex organic molecules. Its perfluorophenyl group imparts unique electronic and steric effects, making it a valuable component in the design of novel organic materials and pharmaceutical intermediates. Chemists leverage the reactivity and stability of $name$ to introduce functional groups, modify molecular structures, and access a diverse range of chemical compounds with tailored properties.Overall, the (R)-2-((tert-butoxycarbonyl)amino)-3-(perfluorophenyl)propanoic acid plays a pivotal role in advancing synthetic chemistry by facilitating the controlled synthesis of chiral and structurally diverse molecules with applications across various industries.