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16771-84-9

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16771-84-9 Usage

General Description

1-Cyclohexyl-4-piperidinone, also known as N-Cyclohexyl-4-piperidone, is a chemical compound with the molecular formula C11H19NO. It is a cyclic amide and a derivative of piperidine, commonly used in the synthesis of pharmaceuticals and agrochemicals. 1-CYCLOHEXYL-4-PIPERIDINONE is also used as a building block in the production of various compounds, including antihistamines, analgesics, and antipsychotic drugs. It is a versatile intermediate in organic chemistry and has a wide range of applications in the pharmaceutical and chemical industries. Additionally, it is an important precursor for the synthesis of other heterocyclic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 16771-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,7 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16771-84:
(7*1)+(6*6)+(5*7)+(4*7)+(3*1)+(2*8)+(1*4)=129
129 % 10 = 9
So 16771-84-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H19NO/c13-11-6-8-12(9-7-11)10-4-2-1-3-5-10/h10H,1-9H2

16771-84-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohexylpiperidin-4-one

1.2 Other means of identification

Product number -
Other names 1-Cyclohexyl-4-piperidone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:16771-84-9 SDS

16771-84-9Relevant articles and documents

Novel symmetrical trans-bis-Schiff bases of N-substituted-4- piperidones: Synthesis, characterization, and preliminary antileukemia activity mensurations

Sun, Chuan-Wen,Wang, Hai-Feng,Zhu, Jun,Yang, Ding-Rong,Xing, Jiahua,Jin, Jia

, p. 1374 - 1380 (2014/01/06)

A series of novel symmetrical trans-bis-Schiff bases (11a, 11b, 11c, 11d, 11e, 11f, 11g, 11h, 11i, 11j, 11k, 11l, 11m) were designed and prepared as novel anticancer analogues, with the trans-configuration confirmed by X-ray diffraction. Preliminary inhibitory effects of these compounds on CML K562 cell growth were investigated, and the potential analogue 11e showed an excellent anti-leukemia activity (IC50=6.35 μg/mL), which is higher than that of the clinical drug 5-fluorouracil (IC50=8.48 μg/mL). Complete assignments had been achieved for the title compounds by spectroscopic techniques, and their structure-activity relationships have been studied.

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

Scherer, T.,Hielkema, W.,Krijnen, B.,Hermant, R. M.,Eijckelhoff, C.,et al.

, p. 535 - 548 (2007/10/02)

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.

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