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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
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, 3,4-dichloro-

OC(=O)[C@@H](Cc1ccc(c(c1)Cl)Cl)N Request for Quotation
Chemical Name: D-Phenylalanine, 3,4-dichloro-
CAS Number: 52794-98-6
Product Number: AG00I9FT(AGN-PC-0OBRNV)
Synonyms:
MDL No:
Molecular Formula: C9H9Cl2NO2
Molecular Weight: 234.0793

Identification/Properties

Computed Properties
Molecular Weight:
234.076g/mol
XLogP3:
-0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
233.001g/mol
Monoisotopic Mass:
233.001g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
213
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,4-Dichloro-D-phenylalanine is a valuable reagent widely used in chemical synthesis for the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. This compound serves as a versatile building block due to its unique chemical properties. In particular, 3,4-Dichloro-D-phenylalanine is commonly utilized in the synthesis of peptide libraries, which are essential tools in drug discovery and development. Its specific structural features make it a valuable tool for introducing diversity into peptide sequences, enabling the creation of novel compounds with potential bioactive properties. Additionally, 3,4-Dichloro-D-phenylalanine can be employed in the preparation of complex natural products and biologically active molecules, contributing significantly to advancements in the field of organic chemistry. Its versatility and compatibility with various reaction conditions make it an indispensable component in the toolkit of synthetic chemists seeking to access structurally diverse molecules for various applications.