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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)-

Benzoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-

O=C(Nc1ccccc1C(=O)O)OCC1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: Benzoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-
CAS Number: 150256-42-1
Product Number: AG001MG0(AGN-PC-0JYVKT)
Synonyms:
MDL No:
Molecular Formula: C22H17NO4
Molecular Weight: 359.3747

Identification/Properties

Computed Properties
Molecular Weight:
359.381g/mol
XLogP3:
4.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
359.116g/mol
Monoisotopic Mass:
359.116g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
528
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Fmoc-2-Abz-OH, or 9-fluorenylmethoxycarbonyl-2-aminobenzoic acid, serves as a valuable building block in chemical synthesis processes. Primarily utilized as a versatile derivative of amino acids, Fmoc-2-Abz-OH plays a crucial role in peptide synthesis. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group shields the amino group, allowing for precise control over the addition and positioning of amino acids in peptide chains. This compound is favored for its compatibility with solid-phase peptide synthesis methods, facilitating the stepwise assembly of complex peptide structures. Additionally, Fmoc-2-Abz-OH offers enhanced stability during peptide cleavage and purification procedures, contributing to the efficiency and success of peptide synthesis endeavors.