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82966-19-6

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82966-19-6 Usage

Description

4-[2-(piperidin-1-yl)ethyl]phenol, also known as 1-(4-hydroxyphenyl)-2-(1-piperidinyl)ethanone, is a chemical compound that features a phenol group and a piperidine ring. This unique structure endows it with potential anticonvulsant and analgesic properties, positioning it as a significant compound in the research and pharmaceutical sectors, particularly for the development of new drugs.

Uses

Used in Pharmaceutical Research and Development:
4-[2-(piperidin-1-yl)ethyl]phenol is utilized as a key component in the development of new drugs due to its potential anticonvulsant and analgesic properties. Its unique structure and properties make it a valuable tool for researchers and scientists in the field of medicinal chemistry, aiding in the study and treatment of neurological and pain-related disorders.
Used in Neurological Disorder Research:
In the field of neurological disorder research, 4-[2-(piperidin-1-yl)ethyl]phenol serves as an important compound for investigating the underlying mechanisms of conditions such as epilepsy and other seizure disorders. Its potential anticonvulsant properties make it a promising candidate for further study and potential therapeutic applications.
Used in Pain Management Research:
4-[2-(piperidin-1-yl)ethyl]phenol is also used in pain management research, where its analgesic properties are explored for the development of novel pain relief therapies. This can be particularly beneficial in conditions where existing treatments are insufficient or have undesirable side effects, offering a potential alternative for patients suffering from chronic or acute pain.

Check Digit Verification of cas no

The CAS Registry Mumber 82966-19-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,6 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 82966-19:
(7*8)+(6*2)+(5*9)+(4*6)+(3*6)+(2*1)+(1*9)=166
166 % 10 = 6
So 82966-19-6 is a valid CAS Registry Number.

82966-19-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-piperidin-1-ylethyl)phenol

1.2 Other means of identification

Product number -
Other names -

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:82966-19-6 SDS

82966-19-6Relevant articles and documents

Discovery of a new class of multi-target heterocycle piperidine derivatives as potential antipsychotics with pro-cognitive effect

Gao, Lanchang,Hao, Chao,Chen, Jiali,Ma, Ru,Zheng, Lu,Wu, Qingkun,Liu, Xin,Liu, Bi-Feng,Zhang, Guisen,Chen, Yin,Jin, Jian

supporting information, (2021/03/19)

A series of benzoisoxazoleylpiperidine derivatives were synthesized by using the multi-target strategies and their potent affinities for dopamine (DA), serotonin (5-HT) and human histamine H3 receptors have been evaluated. Of these compounds, t

LTA4H modulators and uses thereof

-

Page/Page column 36, (2008/12/07)

Leukotriene A4 hydrolase (LTA4H) inhibitors, compositions containing them, and methods of use for the inhibition of LTA4H enzyme activity and the treatment, prevention or inhibition of inflammation and/or conditions associated with inflammation.

2-Phenoxy-indan-1-one derivatives as acetylcholinesterase inhibitors: A study on the importance of modifications at the side chain on the activity

Shen, Yanhong,Sheng, Rong,Zhang, Jing,He, Qiaojun,Yang, Bo,Hu, Yongzhou

, p. 7646 - 7653 (2008/12/23)

As a part of our project aimed at developing new agents of potential application in AD, a new series of 2-phenoxy-indan-1-one derivatives which possess alkylamine side chain were designed, synthesized, and evaluated for their inhibitory activity against AChE and BuChE. Most of the compounds were found to inhibit AChE in the nanomolar range. The optimum inhibitor 3g exhibited 34-fold increase in AChE inhibition than donepezil and displayed neuroprotective effect against H2O2-induced cell death.

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