152902-80-2

Basic information

• Product Name: 4-Piperidineethanol, 1-benzoyl-
• CAS NO: 152902-80-2
• Molecular Formula: C14H19NO2
• Molecular Weight: 233.31
• Mol File: 152902-80-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 4-Piperidineethanol, 1-benzoyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Piperidineethanol, 1-benzoyl-(152902-80-2)
• EPA Substance Registry System: 4-Piperidineethanol, 1-benzoyl-(152902-80-2)

Safety Data

• Hazardous Substances Data: 152902-80-2(Hazardous Substances Data)

Upstream product

• 54108-67-7 N-benzoyl-4-(carbethoxymethyl)piperidine 
• 622-26-4 4-(2-Hydroxyethyl)piperidine 
• 98-88-4 benzoyl chloride 
• 28356-58-3 pyridine-4-acetic acid 
• 5344-27-4 4-(2-hydroxyethyl)pyridine 

Downstream Products

• 223393-97-3 2-ethanal 
• 189177-06-8 (2R,1'S)-2-(1-hydroxy-1-phenyl)methyl-1-azabicyclo[2.2.2]octane 
• 189177-29-5 2-(1-hydroxy-1-phenyl)methyl-1-azabicyclo[2.2.2]octane 
• 223394-05-6 (1S,2S)-3--1,2-dihydroxy-1-(naphth-1-yl)propane 
• 223394-06-7 (1S,2S)-3--1,2-epoxy-1-(nahth-1-yl)propane 
• 223394-04-5 E-3--1-(naphth-1-yl)prop-1-ene 
• 223394-03-4 [4-((E)-3-Naphthalen-1-yl-allyl)-piperidin-1-yl]-phenyl-methanone 
• 223394-19-2 (2S,3S)-4--2,3-epoxy-1-methoxybutane 
• 223394-18-1 (2S,3S)-4--2,3-epoxybutan-1-ol 
• 223394-17-0 4-<(N-benzoyl)piperidin-4-yl>but-2-en-1-ol 
• 189177-06-8 (2R,1'S)-2-(1-phenyl-1-hydroxy)methyl-1-azabicyclo<2.2.2>octane 
• 189177-29-5 (2R,1'R)-2-(1-hydroxy-1-phenyl)methyl-1-azabicyclo<2.2.2>octane 
• 189177-28-4 (2S,1'S)-2-(1-hydroxy-1-phenyl)methyl-1-azabicyclo<2.2.2>octane 
• 189177-30-8 (2S,1'R)-2-(1-phenyl-1-hydroxy)methyl-1-azabicyclo<2.2.2>octane 

Relevant articles and documents

Nitrogenous heterocyclic compound with nematocidal activity, preparation method and application thereof

The invention relates to a nitrogenous heterocyclic compound with nematocidal activity, a preparation method and application thereof. Specifically, the invention discloses a compound with a formula (I) or an optical isomer, cis-trans isomer or acceptable salt in agricultural pharmacology and a preparation method thereof. The invention further discloses an agricultural composition containing the compound and application thereof. The compound has excellent nematocidal activity.

Asymmetric approaches to 2-hydroxymethylquinuclidine derivatives

Highly enantio- and diastereoselective routes to 2- hydroxymethylquinuclidines have been developed. Key steps involve the use of Sharpless dihydroxylation or Sharpless epoxidation to introduce the asymmetry with high stereocontrol, and formation of the quinuclidine ring systems via cyclisation of epoxy amines.

Azolyl-cyclic amine derivates with immunomodulatory activity

A compound of the formula (I), STR1 as defined in the specification, having immunomodulatory activity, or a pharmaceutically acceptable salt thereof, pharmaceutical compositions comprising the compound, and processes to make and to use the compound are described.