CAS 1343040-07-2

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

CAS : 1343040-07-2

Formule : C₂₂H₂₃NO₄

Degré de pureté : 98%

Masse moléculaire : 365.4223

Ref: IN-DA01AJM8

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

CAS : 1343040-07-2

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

Degré de pureté : 98%

Masse moléculaire : 365.42g/mol

Ref: 54-OR77964

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

CAS : 1343040-07-2

Degré de pureté : 98%

Masse moléculaire : 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

Formule : C₂₂H₂₃NO₄

Degré de pureté : Min. 95%

Masse moléculaire : 365.4 g/mol

Ref: 3D-TDC04007