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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)-

L-Cystine, N,N'-bis[(9H-fluoren-9-ylmethoxy)carbonyl]-

O=C(N[C@H](C(=O)O)CSSC[C@@H](C(=O)O)NC(=O)OCC1c2ccccc2c2c1cccc2)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: L-Cystine, N,N'-bis[(9H-fluoren-9-ylmethoxy)carbonyl]-
CAS Number: 135273-01-7
Product Number: AG007ZN2(AGN-PC-0O17L2)
Synonyms:
MDL No:
Molecular Formula: C36H32N2O8S2
Molecular Weight: 684.7779

Identification/Properties

Computed Properties
Molecular Weight:
684.778g/mol
XLogP3:
5.8
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
10
Rotatable Bond Count:
15
Exact Mass:
684.16g/mol
Monoisotopic Mass:
684.16g/mol
Topological Polar Surface Area:
202A^2
Heavy Atom Count:
48
Formal Charge:
0
Complexity:
1010
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (2R,2'R)-3,3'-Disulfanediylbis(2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)propanoic acid) $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure allows for the introduction of specific functional groups and stereochemistry into complex molecules. By incorporating $name$ into synthetic pathways, chemists can achieve precise control over the formation of disulfide bonds, essential for the stability and activity of many biologically active compounds. Additionally, the fluorenyl group in $name$ provides a rigid scaffold that can aid in the design of chiral catalysts or ligands, enhancing the efficiency and selectivity of various chemical reactions. In summary, the application of $name$ in chemical synthesis offers a powerful tool for creating structurally diverse and functionally tailored molecules with potential applications in pharmaceuticals, materials science, and beyond.