672-13-9 Usage
Description
2-Hydroxy-5-methoxybenzaldehyde is a clear yellow liquid with acaricidal activity against Tyrophagus putrescentiae. It is an organic compound that has been utilized in various applications due to its unique chemical properties.
Uses
Used in Chemical Synthesis:
2-Hydroxy-5-methoxybenzaldehyde is used as a key intermediate in the synthesis of tetradentate Schiff base compounds. These compounds are important in various chemical and pharmaceutical applications due to their versatile coordination chemistry and potential use in catalysis and medicinal chemistry.
Used in Pest Control:
2-Hydroxy-5-methoxybenzaldehyde exhibits acaricidal activity against Tyrophagus putrescentiae, making it a potential candidate for use in the development of new pesticides or pest control strategies.
Used in Research and Development:
2-Hydroxy-5-methoxybenzaldehyde is employed in the study of electroantennogram response of the vine weevil (Otiorhynchus sulcatus F.) to a broad range of volatile plant compounds. This research can contribute to a better understanding of the interactions between insects and plants, which can be valuable in agriculture and ecology.
Used in Pharmaceutical Industry:
2-Hydroxy-5-methoxybenzaldehyde has been used in the synthesis of radiolabeling precursor desmethyl-PBR06, which can be utilized in the development of new drugs or drug delivery systems in the pharmaceutical industry.
Used in Organic Chemistry:
2-Hydroxy-5-methoxybenzaldehyde is also used in the preparation of 6-methoxy-3-nitro-2H-chromene using dibutylamine as a reagent. This demonstrates its versatility in organic synthesis and its potential use in creating a variety of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 672-13-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,7 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 672-13:
(5*6)+(4*7)+(3*2)+(2*1)+(1*3)=69
69 % 10 = 9
So 672-13-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H8O3/c1-11-7-2-3-8(10)6(4-7)5-9/h2-5,10H,1H3
672-13-9Relevant articles and documents
The first total syntheses of (±)-Preussomerins K and L using 2-arylacetal anion technology
Quesada, Ernesto,Stockley, Martin,Taylor, Richard J. K.
, p. 4877 - 4881 (2004)
The first syntheses of newly isolated members of the Preussomerin family, Preussomerins K and L, are reported. Key steps include the functionalisation of a 2-arylacetal anion, one-pot Friedel-Crafts cyclisation-deprotection and reductive opening of epoxides.
Phosphine-catalyzed sequential (2+3)/(2+4) annulation of γ-vinyl allenoates: Access to the synthesis of chromeno[4,3-: B] pyrroles
Huang, You,Li, Xiaohu
supporting information, p. 9934 - 9937 (2021/10/12)
A phosphine-catalyzed cascade (2+3)/(2+4) cyclization reaction of γ-vinyl allenoates with aldimine esters has been developed to provide a series of chromeno[4,3-b]pyrrole derivatives that contain three contiguous stereogenic centers. The method gives a good yield, excellent chemoselectivity and diastereoselectivity under mild conditions.
Rh-catalyzed highly regioselective hydroformylation to linear aldehydes by employing porous organic polymer as a ligand
Wang, Zhaozhan,Yang, Yong
, p. 29263 - 29267 (2020/10/06)
In this work, we developed a new structural porous organic polymer containing biphosphoramidite unit, which can be used as a solid bidentate phosphorous ligand for rhodium-catalyzed solvent-free higher olefins hydroformylation. The resultant catalyst demonstrated unprecedently high regioselectivity to linear aldehydes and could be readily recovered for successive reuses with good stability in both catalytic activity and regioselectivity. This journal is