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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)-

Butanoic acid, 3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (3S)-

C[C@H](NC(=O)OCC1c2ccccc2c2c1cccc2)CC(=O)O Request for Quotation
Chemical Name: Butanoic acid, 3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (3S)-
CAS Number: 193954-26-6
Product Number: AG0034YB(AGN-PC-0O6ET4)
Synonyms:
MDL No:
Molecular Formula: C19H19NO4
Molecular Weight: 325.3585

Identification/Properties

Properties
MP:
96-98℃(Solv: hexane (110-54-3); ethyl acetate (141-78-6))
BP:
555.3 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
325.364g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
325.131g/mol
Monoisotopic Mass:
325.131g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
444
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


(S)-3-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]butanoic acid, also known as $name$, plays a crucial role in chemical synthesis as a valuable chiral building block. Its unique structure contains both a fluorenyl group and a protected amino acid moiety, making it versatile in various synthetic pathways.In chemical synthesis, (S)-3-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]butanoic acid is often utilized as a key intermediate for the asymmetric synthesis of biologically active compounds or pharmaceuticals. Its chiral nature imparts stereochemical control in reactions, enabling the formation of enantiomerically pure products.Furthermore, the fluorenyl group in the molecule provides steric hindrance and stability, offering protection to sensitive functional groups during different synthetic steps. This protection is vital in multi-step syntheses to prevent undesired side reactions and ensure the desired stereochemistry of the final product.Overall, (S)-3-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]butanoic acid serves as a versatile tool in chemical synthesis, enabling chemists to access complex molecules with high enantiomeric purity and structural diversity. Its applications extend to the preparation of advanced materials, medicinal chemistry, and the development of new chemical methodologies.