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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-(dipropylamino)-3-(9H-fluoren-9-ylmethoxy)-3-oxopropanoic acid

CCCN(C(C(=O)OCC1c2ccccc2c2c1cccc2)C(=O)O)CCC Request for Quotation
Chemical Name: 2-(dipropylamino)-3-(9H-fluoren-9-ylmethoxy)-3-oxopropanoic acid
CAS Number: 218926-47-7
Product Number: AG007OUK(AGN-PC-09TEWS)
Synonyms:
MDL No: MFCD02092979
Molecular Formula: C23H27NO4
Molecular Weight: 381.4648

Identification/Properties

Computed Properties
Molecular Weight:
381.472g/mol
XLogP3:
5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
9
Exact Mass:
381.194g/mol
Monoisotopic Mass:
381.194g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
28
Formal Charge:
0
Complexity:
521
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-propylpentanoic acid is a versatile compound commonly utilized in chemical synthesis processes. With its unique chemical structure and reactivity profile, this compound is particularly valued for its role as a protecting group in peptide synthesis. By selectively blocking specific functional groups within peptide molecules, this compound enables precise control over the sequential assembly of amino acids during peptide chain elongation. Additionally, the presence of the fluorenyl moiety in this molecule imparts enhanced stability and protection to the amino acid residues, ensuring high yields and purity in the final peptide products. Its application in chemical synthesis extends beyond peptide chemistry, finding utility in the synthesis of various complex organic molecules where protection and selective deprotection steps are crucial for successful transformations.