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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)-

2-Thiophenepropanoicacid, 5-bromo-a-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,(aS)-

O=C(N[C@H](C(=O)O)Cc1ccc(s1)Br)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: 2-Thiophenepropanoicacid, 5-bromo-a-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,(aS)-
CAS Number: 220497-50-7
Product Number: AG00I4BD(AGN-PC-0QYLR4)
Synonyms:
MDL No:
Molecular Formula: C22H18BrNO4S
Molecular Weight: 472.3516

Identification/Properties

Properties
MP:
150.4 °C
BP:
657.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
472.353g/mol
XLogP3:
5.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
7
Exact Mass:
471.014g/mol
Monoisotopic Mass:
471.014g/mol
Topological Polar Surface Area:
104A^2
Heavy Atom Count:
29
Formal Charge:
0
Complexity:
583
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


The (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(5-bromothiophen-2-yl)propanoic acid, also known as $name$, plays a crucial role in chemical synthesis as a key building block. This compound is instrumental in the creation of novel pharmaceuticals, agrochemicals, and materials due to its unique structural features and versatile reactivity.In chemical synthesis, $name$ serves as a chiral intermediate that enables the introduction of the fluorenylmethoxycarbonyl (Fmoc) protecting group. The Fmoc group is widely utilized in peptide synthesis to protect the amine functionality of amino acids during the stepwise assembly of peptides. By incorporating $name$ into the synthesis process, chemists can precisely control the stereochemistry of the final product, leading to the production of enantiomerically pure compounds with high purity and efficacy.Furthermore, the bromothiophene moiety in $name$ confers additional functionality that can be exploited for further diversification and modification through cross-coupling reactions, Suzuki-Miyaura couplings, and other transformations. This flexibility allows for the development of structurally diverse molecules with tailored properties and functions, making $name$ a valuable tool for medicinal chemistry, material science, and other interdisciplinary areas of research.In summary, the application of (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(5-bromothiophen-2-yl)propanoic acid in chemical synthesis offers researchers a powerful tool for the controlled synthesis of complex molecules with specific stereochemical and functional characteristics, driving innovation and advancement in various scientific fields.