132706-25-3 Usage
Uses
Used in Pharmaceutical Industry:
3-Phenoxythiophene-2-carbaldehyde is used as a building block for the development of new drugs due to its potent antibacterial and antifungal properties. It aids in the creation of medications that can effectively combat various infections and diseases.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Phenoxythiophene-2-carbaldehyde serves as a key component in the synthesis of pesticides. Its strong antimicrobial properties contribute to the development of effective pest control solutions for agriculture.
Used in Organic Synthesis:
3-Phenoxythiophene-2-carbaldehyde is utilized as a versatile reagent in organic synthesis. Its unique structure and reactivity make it instrumental in the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in creating a wide range of organic compounds for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 132706-25-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,7,0 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 132706-25:
(8*1)+(7*3)+(6*2)+(5*7)+(4*0)+(3*6)+(2*2)+(1*5)=103
103 % 10 = 3
So 132706-25-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H8OS/c1-2-4-9(5-3-1)11-10-6-7-12-8-10/h1-8H
132706-25-3Relevant academic research and scientific papers
A new biarylphosphine ligand for the Pd-catalyzed synthesis of diaryl ethers under mild conditions
Salvi, Luca,Davis, Nicole R.,Ali, Siraj Z.,Buchwald, Stephen L.
supporting information; experimental part, p. 170 - 173 (2012/03/08)
A new bulky biarylphosphine ligand (L8) has been developed that allows the Pd-catalyzed C-O cross-coupling of a wide range of aryl halides and phenols under milder conditions than previously possible. A direct correlation between the size of the ligand substituents in the 2′, 4′, and 6′ positions of the nonphosphine containing ring and the reactivity of the derived catalyst system was observed. Specifically, the rate of coupling increased with the size of these substituents.
UREA BASED LIPOXYGENASE INHIBITING COMPOUNDS
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, (2008/06/13)
Substituted phenyl, naphthyl, and thienyl N-hydroxy urea compounds form a class of potent inhibitors of 5-and 12-lipoxygenase and are thus useful compounds in the treatment of inflammatory disease states where leukotrienes and other products of lipoxygenase enzyme activity are implicated.
