10035-27-5 Usage
Description
Alpha-guaiaconic acid, with the molecular formula C19H30O4, is a natural chemical compound derived from plants such as Guaiacum officinale, native to the Caribbean and South America. It is recognized for its unique chemical structure and has been the subject of research due to its potential medicinal properties, including antioxidant and anti-inflammatory effects. Additionally, it is utilized in organic synthesis and serves as a building block for the synthesis of other compounds, making it a promising candidate for various applications in pharmaceuticals and other industries.
Uses
Used in Pharmaceutical Industry:
Alpha-guaiaconic acid is used as a medicinal compound for its potential antioxidant and anti-inflammatory effects, which can contribute to the development of treatments for various health conditions.
Used in Organic Synthesis:
Alpha-guaiaconic acid is used as a building block in organic synthesis, enabling the creation of other compounds that can have diverse applications in different industries.
Used in Research and Development:
Due to its unique chemical structure, alpha-guaiaconic acid is used in research and development for exploring its potential applications in pharmaceuticals and other industries, with the aim of discovering new uses and enhancing existing ones.
Check Digit Verification of cas no
The CAS Registry Mumber 10035-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,3 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10035-27:
(7*1)+(6*0)+(5*0)+(4*3)+(3*5)+(2*2)+(1*7)=45
45 % 10 = 5
So 10035-27-5 is a valid CAS Registry Number.
InChI:InChI=1/C20H20O5/c1-11-12(2)20(14-6-8-16(22)18(10-14)24-4)25-19(11)13-5-7-15(21)17(9-13)23-3/h5-10,21-22H,1-4H3
10035-27-5Relevant articles and documents
Efficient Total Synthesis of (±)-Isoguaiacin and (±)-Isogalbulin
Pilkington, Lisa I.,Song, Soo Min,Fedrizzi, Bruno,Barker, David
, p. 1449 - 1452 (2017/07/22)
1-Arylnaphthalene lignans such as (-)-isoguaiacin and (-)-isogalbulin have been reported to exhibit notable biological properties. While (-)-isoguaiacin has not been previously synthesized, syntheses of (-)-isogalbulin are generally long and produce a mixture of stereoisomers. We herein present the efficient total synthesis of (±)-isoguaiacin and (±)-isogalbulin in seven and eight steps with an overall yield of 46% and 36%, respectively. The reported approach harnesses a hydrogenolysis reaction in acidic conditions, to convert a furan into an arylnaphthalen structure.
A novel synthetic route to furan-lignans
Wu, Anxin,Wang, Mingyi,Pan, Xinfu
, p. 2087 - 2091 (2007/10/03)
Three naturally occurring furan-lignans and two analogs have been synthesized by a short and efficient route starting from the corresponding aryl acid. The selective reductive removal of allylic hydroxy by palladium oxide in a mixed solvent of THF-CHCl3 was employed as the key step.
