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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)-

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(methylselanyl)butanoic acid

C[Se]CC[C@@H](C(=O)O)NC(=O)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(methylselanyl)butanoic acid
CAS Number: 1217852-49-7
Product Number: AG001609(AGN-PC-0WAHKE)
Synonyms:
MDL No:
Molecular Formula: C20H21NO4Se
Molecular Weight: 418.3450

Identification/Properties

Computed Properties
Molecular Weight:
418.362g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
8
Exact Mass:
419.064g/mol
Monoisotopic Mass:
419.064g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
478
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:
H317-H319
Precautionary Statements:
P280-P305+P351+P338-P411
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(methylselanyl)butanoic acid, often referred to simply as $name$, plays a crucial role in chemical synthesis as a versatile building block and protecting group for amino acids. Its unique structure allows for selective incorporation into peptide chains, enabling the synthesis of complex and structurally diverse peptides. In addition, the methylselanyl group provides a valuable tool for introducing selenium functionalities into peptides, which can lead to enhanced biological activities or unique chemical reactivity. By utilizing $name$ in chemical synthesis, researchers have the opportunity to construct tailored peptides and study their properties for various applications in medicinal chemistry, biochemistry, and materials science.