94709-12-3 Usage
Description
(3,5-DIMETHOXYPHENYL)(4-METHOXYPHENYL)-METHANONE, commonly known as piperine, is a naturally occurring ketone derivative found in black pepper and related plants. It features two aromatic rings with methoxy groups and has been recognized for its potential pharmacological properties, such as enhancing the bioavailability of certain drugs and exhibiting anti-inflammatory and antioxidant effects. Piperine is also valued for its pungent taste and has been utilized in traditional medicine and as a seasoning in various cuisines for centuries. However, ongoing research is necessary to fully comprehend its impact on human health.
Uses
Used in Pharmaceutical Industry:
(3,5-DIMETHOXYPHENYL)(4-METHOXYPHENYL)-METHANONE is used as a bioavailability enhancer for certain drugs, improving the absorption and effectiveness of these medications within the body.
Used in Nutraceutical Industry:
(3,5-DIMETHOXYPHENYL)(4-METHOXYPHENYL)-METHANONE is used as a supplement for its potential anti-inflammatory and antioxidant properties, contributing to overall health and well-being.
Used in Traditional Medicine:
(3,5-DIMETHOXYPHENYL)(4-METHOXYPHENYL)-METHANONE is used in traditional medicine practices for its long-standing reputation as a remedy for various ailments, leveraging its historical use and therapeutic potential.
Used in Culinary Industry:
(3,5-DIMETHOXYPHENYL)(4-METHOXYPHENYL)-METHANONE is used as a seasoning in various cuisines, adding a distinctive pungent flavor to dishes and enhancing the overall taste experience.
Check Digit Verification of cas no
The CAS Registry Mumber 94709-12-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,7,0 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 94709-12:
(7*9)+(6*4)+(5*7)+(4*0)+(3*9)+(2*1)+(1*2)=153
153 % 10 = 3
So 94709-12-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H16O4/c1-18-13-6-4-11(5-7-13)16(17)12-8-14(19-2)10-15(9-12)20-3/h4-10H,1-3H3
94709-12-3Relevant articles and documents
Highly Selective and Divergent Acyl and Aryl Cross-Couplings of Amides via Ir-Catalyzed C-H Borylation/N-C(O) Activation
Gao, Pengcheng,Szostak, Michal
supporting information, p. 6010 - 6015 (2020/07/30)
Herein, we demonstrate that amides can be readily coupled with nonactivated arenes via sequential Ir-catalyzed C-H borylation/N-C(O) activation. This methodology provides facile access to biaryl ketones and biaryls by the sterically controlled Ir-catalyzed C-H borylation and divergent acyl and decarbonylative amide N-C(O) and C-C activation. The methodology diverts the traditional acylation and arylation regioselectivity, allowing us to directly utilize readily available arenes and amides to produce valuable ketone and biaryl motifs.
Palladium nanoparticles supported on a nickel pyrazolate metal organic framework as a catalyst for Suzuki and carbonylative Suzuki couplings
Augustyniak,Zawartka,Navarro,Trzeciak
supporting information, p. 13525 - 13531 (2016/09/04)
Methanolic reduction of [PdCl2(CH3CN)2] on a [Ni(2,5-di(1H-pyrazol-4-yl)benzenesulfonate)2] metal organic framework gives rise to Pd2+/Pd0 nanocomposites with Suzuki and carbonylative Suzuki heterogeneous catalytic activities.
