94635-24-2

Basic information

• Product Name: CHEMBRDG-BB 4000321
• Synonyms: CHEMBRDG-BB 4000321;1-(4-Methoxy-phenyl)-piperidin-4-one;UKRORGSYN-BB BBV-086497;1-(4-methoxyphenyl)piperidin-4-one(SALTDATA: FREE)
• CAS NO: 94635-24-2
• Molecular Formula: C₁₂H₁₅NO₂
• Molecular Weight: 205.25
• Product Categories: CHIRAL CHEMICALS
• Mol File: 94635-24-2.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 371.9°C at 760 mmHg
• Flash Point: 178.7°C
• Appearance: /
• Density: 1.126g/cm³
• Vapor Pressure: 1E-05mmHg at 25°C
• Refractive Index: 1.548
• CAS DataBase Reference: CHEMBRDG-BB 4000321(CAS DataBase Reference)
• NIST Chemistry Reference: CHEMBRDG-BB 4000321(94635-24-2)
• EPA Substance Registry System: CHEMBRDG-BB 4000321(94635-24-2)

Safety Data

• Hazardous Substances Data: 94635-24-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H15NO2/c1-15-12-4-2-10(3-5-12)13-8-6-11(14)7-9-13/h2-5H,6-9H2,1H3

Upstream product

• 3592-25-4 1,5-dichloropentan-3-one 
• 104-94-9 4-methoxy-aniline 
• 696-62-8 para-iodoanisole 
• 56525-68-9 3,3'-(4-methoxy-phenylimino)-di-propionic acid diethyl ester 
• 177-11-7 4,4-ethylenedioxy-piperidine 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 634904-81-7 8-(4-methoxyphenyl)-1,4-dioxa-8-azaspiro[4.5]decane 
• 94635-23-1 ethyl 1-(p-methoxyphenyl)-4-oxo-3-piperidinecarboxylate 

Downstream Products

• 154913-15-2 1-(4-Methoxyphenyl)-4-(1-naphthyl)-4-piperidinol 
• 154913-01-6 1-(4-Methoxyphenyl)-4-<(4-cyano-1-naphthyl)methylene>piperidine 
• 94635-25-3 ethyl cyano-[1-(p-methoxyphenyl)-4-piperidinylidene]acetate 
• 120883-66-1 N-(p-Methoxyphenyl)-4-azacyclohexylidenemalononitrile 
• 94635-27-5 2,6-Diamino-5-[1-(4-methoxy-phenyl)-piperidin-4-yl]-pyrimidin-4-ol 
• 94635-22-0 2,4-diamino-6-chloro-5-[1-(4-methoxyphenyl)-4-piperidinyl]pyrimidine 
• 94635-26-4 Cyano-[1-(4-methoxy-phenyl)-piperidin-4-yl]-acetic acid ethyl ester 
• 259663-88-2 1-(4-methoxyphenyl)-4-aminopiperidine 
• 147328-61-8 1-(1-Phenyl-4-piperidyl)-4-<(4-cyano-1-naphthyl)methylene>piperidine 
• 154912-91-1 1-(1-Phenyl-4-piperydyl)-4-piperidone 
• 63921-23-3 1-phenylpiperidin-4-ylamine 
• 267428-40-0 1-[1-(4-methoxyphenyl)-4-piperidyl]-4-piperidinone 
• 1005458-22-9 3-[1-(4-methoxy-phenyl)-1,2,3,6-tetrahydro-pyridin-4-yl]-1H-indole-6-carboxylic acid hydrochloride 
• 259663-87-1 1-(4-methoxyphenyl)-4-piperidinone oxime 

Relevant articles and documents

NOVEL TETRAHYDROPYRIDOPYRIMIDINES AND TETRAHYDROPYRIDOPYRIDINES FOR THE TREATMENT AND PROPHYLAXIS OF HEPATITIS B VIRUS INFECTION

The invention provides novel compounds having the general formula (I): wherein R1, R2, R3, Q, U,W, Z, X and Y are as described herein, compositions including the compounds and methods of using the compounds. These compounds are HbsAg inhibitors and are useful as medicaments for the treatment or prophylaxis of HBV infection.

An improved synthesis of N-aryl and N-heteroaryl substituted piperidones

An efficient Pd(0)-catalyzed protocol for the rapid and efficient preparation of N-aryl and N-heteroaryl substituted piperidones is described. The two step syntheses proceed with an overall yield of 50-70% using X-Phos as optimal ligand for the Pd(0)-cata

Synthesis and exploratory photophysical investigation of donor-bridge-acceptor systems derived from N-substituted 4-piperidones

We report a two-step synthesis for N-aryl- and N-alkyl-substituted 4-piperidones, in which the N substituent can easily be varied.A number of intramolecular donor-acceptor systems was synthesized from these piperidones by conversion of the carbonyl functionality.The influence of the N-aryl donor on the electronic absorption and fluorescence spectra was investigated systematically.It was concluded that some systems can be used as efficient fluorescent probes with a high sensitivity for solvent polarity.