N-Boc-1,4-cyclohexanediamine

CAS : 195314-59-1

Ref. 3D-FB15308

Informations sur le produit

• Nom: N-Boc-1,4-cyclohexanediamine
• Synonymes: Tert-butyl 4-aminocyclohexylcarbamate, (4-Amino-Cyclohexyl)-Carbamic Acid Tert-Butyl Ester, (4-Aminocyclohexyl)carbamic acid tert-butyl ester, 1,1-Dimethylethyl N-(4-aminocyclohexyl)carbamate, 1-Boc-Amino-1,4-Cyclohexanediamine, 1-N-Boc-1,4-Cyclohexanediamine, 4-[(Tert-Butoxycarbonyl)Amino]Cyclohexanaminium, Boc-1,4-trans-DACH*HCl, Butyl 4-Aminocyclohexylcarbamate, Carbamic acid, (4-aminocyclohexyl)-, 1,1-dimethylethyl ester, Carbamic acid, N-(4-aminocyclohexyl)-, 1,1-dimethylethyl ester, N-Boc-1,4-Diaminecyclohexane, N-tert-Butoxycarbonylcis-1,4-cyclohexanediamine, Tert-Butyl (4-Aminocyclohexyl)Carbamate, Trans-N-box-1,4-cyclohexanediamine, tert-Butyl 4-aminocyclohexylcarbamate, tert-butyl N-(4-aminocyclohexyl)carbamate, trans-1,4-Diaminocyclohexane, N1-BOC protected

Description

N-Boc-1,4-cyclohexanediamine is a linker that is metabolized by the liver enzymes and has high affinity for the human receptor. It has been found to be an antagonist of the phenyl ring in a number of metabolic pathways. N-Boc-1,4-cyclohexanediamine is synthesized through the reaction of 1,4-cyclohexanediamine with dihydrochloride. The product yield can be optimized by optimizing the synthesis method and selectivity. The pharmacophore of this compound may be used as a lead compound in drug discovery programs.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 214.3 g/mol
• Formule: C₁₁H₂₂N₂O₂
• Degré de pureté: Min. 95%
• Couleur/Forme: White To Yellow Solid
• InChI: InChI=1S/C11H22N2O2/c1-11(2,3)15-10(14)13-9-6-4-8(12)5-7-9/h8-9H,4-7,12H2,1-3H3,(H,13,14)
• Code InChI: InChIKey=FEYLUKDSKVSMSZ-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)NC1CCC(N)CC1