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  2. [1,1'-Biphenyl]-3-propanoic acid,a-amino-2',4'-dichloro-4-hydroxy-5-(phosphonomethyl)-, (aS)-

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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)-

[1,1'-Biphenyl]-3-propanoic acid,a-amino-2',4'-dichloro-4-hydroxy-5-(phosphonomethyl)-, (aS)-

OC(=O)[C@H](Cc1cc(cc(c1O)CP(=O)(O)O)c1ccc(cc1Cl)Cl)N Request for Quotation
Chemical Name: [1,1'-Biphenyl]-3-propanoic acid,a-amino-2',4'-dichloro-4-hydroxy-5-(phosphonomethyl)-, (aS)-
CAS Number: 174575-40-7
Product Number: AG018PR5(AGN-PC-0QAKIA)
Synonyms:
MDL No: MFCD02262130
Molecular Formula: C16H16Cl2NO6P
Molecular Weight: 420.1811

Identification/Properties

Computed Properties
Molecular Weight:
420.179g/mol
XLogP3:
-0.9
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
6
Exact Mass:
419.009g/mol
Monoisotopic Mass:
419.009g/mol
Topological Polar Surface Area:
141A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
547
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


SDZ 220-040 is a highly versatile and valuable compound in chemical synthesis, particularly in the pharmaceutical and agrochemical industries. This compound serves as a key building block for the creation of various complex molecules, thanks to its unique structure and reactivity. In synthetic organic chemistry, SDZ 220-040 is commonly employed as a reagent for introducing specific functional groups or stereocenters into target molecules with high efficiency and selectivity. Its use in cross-coupling reactions, asymmetric transformations, and heterocycle synthesis has been well-documented, showcasing its importance in the development of new drugs, pesticides, and other biologically active compounds. Additionally, SDZ 220-040 exhibits excellent compatibility with a wide range of substrates and reaction conditions, making it a preferred choice for chemists seeking to streamline their synthetic pathways and enhance the overall efficiency of their processes. By harnessing the synthetic power of SDZ 220-040, researchers can expedite the discovery and development of novel chemical entities with potential applications in various fields, driving innovation and progress in the realm of chemical science.