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5164-79-4

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5164-79-4 Usage

Description

(Z,Z)-4-(2-butenylidene)-3,5,5-trimethylcyclohex-2-en-1-one, commonly known as piperlongumine, is a naturally occurring alkaloid derived from long pepper and black pepper. It has garnered significant attention for its potential pharmacological properties, which include anti-cancer, anti-inflammatory, and anti-oxidant effects. Piperlongumine has demonstrated the ability to inhibit the growth of various cancer cells and induce apoptosis, making it a promising compound for further research and potential therapeutic applications.

Uses

Used in Pharmaceutical Applications:
Piperlongumine is used as a therapeutic agent for its anti-cancer properties, particularly in the treatment of various types of cancer. It has shown promising results in inhibiting the growth of cancer cells and inducing apoptosis, which could lead to the development of novel cancer treatments.
Used in Anti-Inflammatory Applications:
As an anti-inflammatory agent, piperlongumine is used to modulate the immune system and reduce inflammation. Its potential to alleviate inflammation-related conditions makes it a valuable compound for the development of new anti-inflammatory medications.
Used in Antioxidant Applications:
Piperlongumine's anti-oxidant properties make it a candidate for use in applications aimed at reducing oxidative stress and protecting cells from damage. This could have implications for the development of treatments for a range of conditions associated with oxidative stress, such as neurodegenerative diseases and cardiovascular disorders.
Used in Research and Development:
Due to its unique chemical structure and bioactive properties, piperlongumine is used as a compound of interest in research and development for the discovery of new therapeutic agents and the advancement of our understanding of various biological processes.
Used in Nutraceutical Applications:
Piperlongumine's potential health benefits may also make it a valuable ingredient in the development of nutraceutical products, which could be used to support overall health and well-being.
Used in Cosmetic Applications:
Given its anti-oxidant and anti-inflammatory properties, piperlongumine could be utilized in the cosmetic industry for the development of products aimed at promoting skin health and reducing signs of aging or inflammation.
Used in Food Industry:
As a natural compound with potential health benefits, piperlongumine may also find applications in the food industry, where it could be incorporated into products as a functional ingredient to enhance their health-promoting properties.

Check Digit Verification of cas no

The CAS Registry Mumber 5164-79-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,6 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5164-79:
(6*5)+(5*1)+(4*6)+(3*4)+(2*7)+(1*9)=94
94 % 10 = 4
So 5164-79-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H18O/c1-5-6-7-12-10(2)8-11(14)9-13(12,3)4/h5-8H,9H2,1-4H3

5164-79-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-4-<(Z)-But-2-enylidene>-3,5,5-trimethylcyclohex-2-enone

1.2 Other means of identification

Product number -
Other names 4-[(Z)-But-2-en-(Z)-ylidene]-3,5,5-trimethyl-cyclohex-2-enone

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:5164-79-4 SDS

5164-79-4Downstream Products

5164-79-4Relevant articles and documents

Novel synthesis of degradation products of carotenoids, megastigmatrienone analogues and blumenol-A

Ito, Nobuhiko,Etoh, Takeaki,Hagiwara, Hisahiro,Kato, Michiharu

, p. 1571 - 1579 (2007/10/03)

Synthesis of 4-alkylidene-3,5,5-trimethylcyclohex-2-enones 7 has been achieved utilising 1,4-conjugate dehydrobromination of allylic bromides 5 as a key step. This chemical transformation is applied to the synthesis of degradation products of carotenoids: megastigmatrienones 7e/1-4,4-methylene-3,5,5-trimethylcyclohex-2-enone 7a, 4-(3-hydroxybutylidene)-3,5,5-trimethylcyclohex-2-enone 9,1,3,7,7-tetramethyl-2-oxabicyclo[4.4.0]dec-5-en-9-one 10a-b and 3,4,7,8-tetrahydro-4,4,7-trimethylnaphthalen-2(6H)-one 15. A novel photoisomerisation of 4-[(Z)-3-acetoxybut-2-enyl]-4-hydroxy-3,5,5-trimethylcyclohex-2-enone 19 to 4-[(E)-3-acetoxybut-2-enyl]-4-hydroxy-3,5,5-trimethylcyclohex-2-enone 20 enables us to synthesise blumenol-A 21.

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