1-Boc-3-aminopiperidine

CAS : 184637-48-7

Ref. 3D-FB31217

Informations sur le produit

• Nom: 1-Boc-3-aminopiperidine
• Synonymes: 3-Aminopiperidine-1-carboxylic acid tert-butyl ester, Dl-3-Amino-1-N-Boc-Piperidine, 1-N-Boc-3-Aminopiperidine, 1-Piperidinecarboxylic Acid, 3-Amino-, 1,1-Dimethylethyl Ester, (+/-)-1-Boc-3-Amino-Piperidine, 3-Aminopiperidine, N1-Boc Protected, (+/-)-3-Amino-1-Boc-Piperidine, 3-Amino-1-Tertbutoxycarbonyl-Piperidine, Tert-Butyl 3-Aminopiperidine-1-Carboxylate, N-1-Boc-3-Aminopiperidine, 1-Boc-3-Aminopiperidine Citric Acid Salt, (+/-)-3-Amino-1-N-Boc-Piperidine, N-BOC-3-Aminopiperidine, (3S)-1-(tert-butoxycarbonyl)piperidin-3-aminium, (3R)-1-(tert-butoxycarbonyl)piperidin-3-aminium, 1-Boc-3-aminopiperidine citric acid, 3-Amino-Piperidine-1-Carboxylic Acid Tert-Butyl Ester

Description

1-Boc-3-aminopiperidine is an aminopiperidine that is used as a feedstock in the manufacture of pharmaceuticals. It is an optical isomer of 1-Boc-4-aminopiperidine, which has been shown to be effective in the synthesis of arylated piperidines. The compound reacts with sodium hypochlorite and formamide to produce ethyl formate, carbamate, and citric acid. The reaction also produces chiral regiospecificity in the product. This drug has been immobilized on silica gel for use in organic synthesis.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 200.28 g/mol
• Formule: C₁₀H₂₀N₂O₂
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C10H20N2O2/c1-10(2,3)14-9(13)12-6-4-5-8(11)7-12/h8H,4-7,11H2,1-3H3
• Code InChI: InChIKey=AKQXKEBCONUWCL-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)N1CCCC(N)C1