CAS 1240529-14-9

Formule : C13H15NO

InChI : InChI=1S/C13H15NO/c15-13-11-6-12(13)9-14(8-11)7-10-4-2-1-3-5-10/h1-5,11-12H,6-9H2

Code InChI : DXLWDHDUFRJNJZ-UHFFFAOYSA-N

SMILES : C1C2CN(CC1C2=O)CC3=CC=CC=C3

3-Benzyl-3-azabicyclo[3.1.1]heptan-6-one

CAS : 1240529-14-9

3-Benzyl-3-azabicyclo[3.1.1]heptan-6-one

Formule : C₁₃H₁₅NO

Degré de pureté : 95%

Masse moléculaire : 201.27

Ref: 54-OR1045058

3-Benzyl-3-azabicyclo[3.1.1]heptan-6-one

CAS : 1240529-14-9

Formule : C₁₃H₁₅NO

Degré de pureté : 97%

Couleur et forme : Solid

Masse moléculaire : 201.2643

Ref: IN-DA00A3XP

3-Benzyl-3-azabicyclo[3.1.1]heptan-6-one

CAS : 1240529-14-9

3-Benzyl-3-azabicyclo[3.1.1]heptan-6-one

Formule : C₁₃H₁₅NO

Degré de pureté : 95%

Masse moléculaire : 201.26

Ref: IN-DG292354

3-BENZYL-3-AZABICYCLO[3.1.1]HEPTAN-6-ONE

CAS : 1240529-14-9

Formule : C₁₃H₁₅NO

Degré de pureté : 95%

Masse moléculaire : 201.269

Ref: 10-F389352

3-benzyl-3-azabicyclo[3.1.1]heptan-6-one

CAS : 1240529-14-9

3-benzyl-3-azabicyclo[3.1.1]heptan-6-one (BAH) is a selective derivatization reagent that reacts with ketones to form cyclobutanes, which are more stable than the corresponding ketones. The product is selectively derivatized at the nitrogen atom of the piperidine ring. BAH is used as a chemical intermediate in medicinal chemistry, such as for the synthesis of piperidines and other heterocycles. This compound has been shown to be efficient in converting 1,2-dihydropyridines into 1,2-dihydroquinolines with high yields and high levels of purity. BAH is also used for the synthesis of multigram quantities of peptides and proteins by postsynthetic modifications on natural amino acids or unnatural amino acids with reactive functional groups such as azide or bromide.

Formule : C₁₃H₁₅NO

Degré de pureté : Min. 95%

Masse moléculaire : 201.27 g/mol

Ref: 3D-QZB52914