CAS 1343040-07-2

Fórmula: C22H23NO4

InChI: InChI=1S/C22H23NO4/c24-21(25)13-23(15-7-1-2-8-15)22(26)27-14-20-18-11-5-3-9-16(18)17-10-4-6-12-19(17)20/h3-6,9-12,15,20H,1-2,7-8,13-14H2,(H,24,25)

Clave InChI: LVJZUYHCQLIJSA-UHFFFAOYSA-N

SMILES: C1CCC(C1)N(CC(=O)O)C(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24

N-(((9h-Fluoren-9-yl)methoxy)carbonyl)-N-cyclopentylglycine

CAS: 1343040-07-2

N-(((9h-Fluoren-9-yl)methoxy)carbonyl)-N-cyclopentylglycine

Fórmula: C₂₂H₂₃NO₄

Pureza: 98%

Peso molecular: 365.42

Ref: 54-OR77964

N-(((9h-Fluoren-9-yl)methoxy)carbonyl)-N-cyclopentylglycine

CAS: 1343040-07-2

Fórmula: C₂₂H₂₃NO₄

Pureza: 98%

Forma y color: Solid

Peso molecular: 365.4223

Ref: IN-DA01AJM8

Fmoc-N-cPent-Gly-OH

CAS: 1343040-07-2

N-Fmoc-N-cyclopentylglycine

Fórmula: C₂₂H₂₃NO₄

Pureza: 98%

Peso molecular: 365.42

Ref: IN-DG00807917

N-(((9h-Fluoren-9-yl)methoxy)carbonyl)-N-cyclopentylglycine

CAS: 1343040-07-2

Pureza: 98%

Peso molecular: 365.4289856

Ref: 10-F634020

2-{Cyclopentyl[(9H-fluoren-9-ylmethoxy)carbonyl]amino}acetic acid

CAS: 1343040-07-2

The synthesis of 2-{Cyclopentyl[(9H-fluoren-9-ylmethoxy)carbonyl]amino}acetic acid is accomplished through an asymmetric, stereoselective, catalytic route. The first step in the synthesis is conversion of glycine to the corresponding N-protected glycine methyl ester by reaction with benzyl chloroformate followed by protection of both carboxylic acid groups as FMOC derivatives. The key steps are a diastereoselective hydrogenation of the cyclopentane ring system and an efficient alkylation reaction of the resulting alcohol with 9H-fluoren-9-ol. 2-[Cyclopentyl[(9H-fluoren-9-ylmethoxy)carbonyl]amino]acetic acid has been shown to be a potent inhibitor against bacterial growth. It binds to bacterial topoisomerase IV enzyme, which

Fórmula: C₂₂H₂₃NO₄

Pureza: Min. 95%

Peso molecular: 365.4 g/mol

Ref: 3D-TDC04007