(R)-3-methyl-1-((3aS,4S,6S,7aR)-3a,5,5-trimethylhexahydro-4,6-methanobenzo[d][1,3,2]dioxaborol-2-yl)butan-1-amine 2,2,2-trifluoroacetate

(R)-3-methyl-1-((3aS,4S,6S,7aR)-3a,5,5-trimethylhexahydro-4,6-methanobenzo[d][1,3,2]dioxaborol-2-yl)butan-1-amine 2,2,2-trifluoroacetate

(2R,3S,5S)-3-(benzyloxy)-5-[2-[[(4-methoxyphenyl)diphenylmethyl]amino]-6-(phenylmethoxy)-9H-purin-9-yl]-2-(benzyloxymethyl)cyclopentanol

(2R,3S,5S)-3-(benzyloxy)-5-[2-[[(4-methoxyphenyl)diphenylmethyl]amino]-6-(phenylmethoxy)-9H-purin-9-yl]-2-(benzyloxymethyl)cyclopentanol

2-amino-1,9-dihydro-9-[(1S,3R,4S)-4-(benzyloxy)-3-(benzyloxymethyl)-2-methylenecyclopentyl]-6H-purin-6-one

$300.00
CAS No.: 142217-81-0
Catalog No.: 109920
Purity: 95%
MF: C26H27N5O3
MW: 457.534
Storage: 2-8 degree Celsius
SMILES: NC1=NC2=C(N=CN2[C@H]2C[C@H](OCC3=CC=CC=C3)[C@@H](COCC3=CC=CC=C3)C2=C)C(=O)N1
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2-amino-1,9-dihydro-9-[(1S,3R,4S)-4-(benzyloxy)-3-(benzyloxymethyl)-2-methylenecyclopentyl]-6H-purin-6-one; CAS No.: 142217-81-0; ChemShuttle offers building blocks for drug discovery like this 2-aminopurinone cyclopentyl derivative, designed as a kinase inhibitor core. The exo-methylene group and benzyl-protected hydroxyls enable Diels-Alder diversification. Our synthetic routes emphasize regioselective purine alkylation and Mitsunobu reactions for cyclopentane attachment. The product s planar adenine mimicry supports ATP-binding pocket targeting in oncology lead optimization programs.

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