CAS 3612-20-2
:1-benzil-4-piperidona
- 1-(Phenylmethyl)-4-piperidinone
- 1-(Phenylmethyl)-4-piperidone
- 1-Bencil-4-Piperidona
- 1-Benzyl-4-Oxopiperidine
- 1-Benzyl-4-Oxopiperidinium
- 1-Benzyl-4-Pipridine
- 1-Benzyl-4-piperidinone
- 1-Benzyl-4-piperidon
- 1-Benzyl-4-piperidone
- 1-Benzylpiperidin-4-one
- 1-Benzylpiperidine-4-one
- 1-Benzylpiperidone
- 4-N-Benzylpiperidone
- 4-Piperidinone, 1-(phenylmethyl)-
- 4-Piperidone, 1-benzyl-
- N-Benzyl-4-Piperidine
- N-Benzyl-4-oxopiperidine
- N-Benzyl-4-piperidinone
- N-Benzylpiperidinone
- N-Benzylpiperidone
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1-Benzyl-4-piperidone, 98+%
CAS:1-Benzyl-4-piperidone is a pharmaceutical intermediate, it is used in penfluridol synthesis of bulk drugs. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa
Fórmula:C12H15NOPureza:98+%Cor e Forma:Clear colorless to yellow, LiquidPeso molecular:189.261-Benzylpiperidin-4-one
CAS:1-Benzylpiperidin-4-oneFórmula:C12H15NOPureza:98%Cor e Forma: very dark yellow to orange liquidPeso molecular:189.25g/mol1-Benzyl-4-piperidone
CAS:Fórmula:C12H15NOPureza:>98.0%(GC)(T)Cor e Forma:Colorless to Yellow clear liquidPeso molecular:189.26N-Benzyl-4-piperidone
CAS:Produto ControladoApplications A substituted piperidine as pesticide.
References Nishizawa, R., et al.: Bioorg. Med. Chem. Lett., 20, 763 (2010), Liras, S., et al.: Bioorg. Med. Chem. Lett., 20, 503 (2010),Fórmula:C12H15NOCor e Forma:NeatPeso molecular:189.3N-Benzyl-4-piperidone
CAS:Produto ControladoN-Benzyl-4-piperidone is a potent antagonist of the histamine H1 receptor. It binds to the receptor in vivo, and it has been shown that this binding leads to a decrease in the release of neurotransmitters in the central nervous system. This drug is used for the treatment of hiv infection and for other conditions such as allergic rhinitis, chronic idiopathic urticaria, and vasomotor rhinitis. N-Benzyl-4-piperidone inhibits the reaction between propionyl chloride and dibutyltin oxide to form a dialkyl tin compound by an acylation reaction. The low energy released during this reaction may be due to hydrogen bonding between this drug and water molecules.
Fórmula:C12H15NOPureza:Min. 95%Cor e Forma:Colorless Clear LiquidPeso molecular:189.25 g/molRef: IN-DA0032OI
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