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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,N-[(9H-fluoren-9-ylmethoxy)carbonyl]-2-nitro-

O=C(N[C@@H](C(=O)O)Cc1ccccc1[N+](=O)[O-])OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: D-Phenylalanine,N-[(9H-fluoren-9-ylmethoxy)carbonyl]-2-nitro-
CAS Number: 478183-70-9
Product Number: AG00D8GF(AGN-PC-0RWN05)
Synonyms:
MDL No:
Molecular Formula: C24H20N2O6
Molecular Weight: 432.4254

Identification/Properties

Computed Properties
Molecular Weight:
432.432g/mol
XLogP3:
4.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
7
Exact Mass:
432.132g/mol
Monoisotopic Mass:
432.132g/mol
Topological Polar Surface Area:
121A^2
Heavy Atom Count:
32
Formal Charge:
0
Complexity:
673
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

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 compound (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-nitrophenyl)propanoic acid, also known as $name$, serves a crucial role in chemical synthesis as a versatile building block. Its unique structure allows for selective manipulation of stereochemistry and functional groups, making it valuable in the creation of complex molecules. Specifically, (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-nitrophenyl)propanoic acid can be utilized as a chiral starting material in the synthesis of pharmaceutical intermediates, agrochemicals, and specialty chemicals. Its presence enhances the efficiency and specificity of synthetic reactions, enabling the production of diverse compounds with desired properties and activities.