4-N-Boc-aminocyclohexanone

CAS: 179321-49-4

Ref. 3D-FB12555

Produktinformation

• Name: 4-N-Boc-aminocyclohexanone
• Synonyme: Tert-Butyl 4-Oxocyclohexylcarbamate, Boc-4-Aminocyclohexanone, (4-Oxo-Cyclohexyl)-Carbamic Acidtert-Butylester, 4-N-Boc-Aminocyclohexanone, 4-N-Boc-4-Aminocyclohexanone, 4-Aminocyclohexanonen-Bocprotected, N-T-Boc-4-Aminocyclohexanone, Tert-Butyl4-Oxocyclohexylcarbamate, Carbamicacid,(4-Oxocyclohexyl)-,1,1-Dimethylethylester, 4-(Boc-Amino)Cyclohexanone, 4-(Tert-Butoxycarbonylamino)Cyclohexanone, 4-N-Boc-Aminocyclohexanone4, N-Boc-4-Aminocyclohexanone, 4-(Tert-Butyloxycarbonylamino)Cyclohexanone, Tert-Butyl 4-Oxocyclohexylacarbamate, tert-butyl N-(4-oxocyclohexyl)carbamate

Beschreibung

4-N-Boc-aminocyclohexanone is a chemical that inhibits the proliferation of cancer cells in vitro. It also has an antiproliferative effect on fibroblast cells, which may be due to its ability to inhibit protein synthesis and induce cell death by apoptosis. 4-N-Boc-aminocyclohexanone can also be used for the preparation of photoresponsive polymers that are used in drug delivery systems. This compound can be prepared by reacting 4-aminocyclohexanol with formaldehyde in the presence of base. This reaction forms a five-membered ring via an amide bond. The amide group is then hydrolyzed to form the corresponding carboxylic acid. The colorimetric method is used to determine the degree of hydrolysis, which is determined by measuring the absorbance at 590 nm. In addition, this compound can be used as a reactive intermediate for other compounds like

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 213.27 g/mol
• Formel: C₁₁H₁₉NO₃
• Reinheit: Min. 95%
• Farbe/Form: White To Light (Or Pale) Yellow Solid
• InChl: InChI=1S/C11H19NO3/c1-11(2,3)15-10(14)12-8-4-6-9(13)7-5-8/h8H,4-7H2,1-3H3,(H,12,14)
• InChI Key: InChIKey=WYVFPGFWUKBXPZ-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)NC1CCC(=O)CC1