184360-97-2 Usage
Uses
Used in Pharmaceutical Industry:
2,3-(Methylenedioxy)benzaldehyde is utilized as an intermediate in the synthesis of various pharmaceuticals for its ability to facilitate the creation of complex organic compounds that can be used in medicinal formulations.
Used in Flavor and Fragrance Industry:
2,3-(METHYLENEDIOXY)BENZALDEHYDE is employed as a key ingredient in the production of fragrances and flavorings due to its distinctive sweet, floral odor, enhancing the sensory profiles of various consumer products.
Used in Organic Synthesis:
2,3-(Methylenedioxy)benzaldehyde is used as a precursor in organic synthesis for its capacity to participate in a range of chemical reactions, contributing to the development of new compounds and materials.
Used in Antimicrobial Applications:
2,3-(Methylenedioxy)benzaldehyde is used as an antifungal and antibacterial agent, leveraging its pharmacological properties to combat microbial infections and promote health and hygiene in various settings.
Used in Research and Development:
2,3-(METHYLENEDIOXY)BENZALDEHYDE is also used in research and development settings to explore its potential applications and to study its chemical properties, furthering scientific understanding and innovation in related fields.
Check Digit Verification of cas no
The CAS Registry Mumber 184360-97-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,3,6 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 184360-97:
(8*1)+(7*8)+(6*4)+(5*3)+(4*6)+(3*0)+(2*9)+(1*7)=152
152 % 10 = 2
So 184360-97-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H6O3/c9-4-6-2-1-3-7-8(6)11-5-10-7/h1-4H,5H2
184360-97-2Relevant academic research and scientific papers
Synthesis of 1-tetralone derivatives using a Stille cross coupling/friedel crafts acylation sequence
Vercouillie, Johnny,Abarbri, Mohamed,Parrain, Jean-Luc,Duchene, Alain,Thibonnet, Jerome
, p. 3751 - 3762 (2007/10/03)
An efficient method of synthesis of 1-tetralones has been achieved featuring a Stille cross-coupling reaction as the key step.
Stereoselective access to functionalized β-γ unsaturated acids
Thibonnet, Jér?me,Abarbri, Mohamed,Parrain, Jean-Luc,Duchêne, Alain
, p. 4433 - 4441 (2007/10/03)
Stereoselective synthesis of vinylstannanes bearing a carboxylic acid function was achieved from β-γ alkynoic acids via hydrostannation, stannylcupration or silastannation reactions. Regioselectivity is highly dependent on the nature of the stannylanions used and on protection of the carboxylic acid function.
Tributylstannyl 4-tributylstannylbut-3-enoate: A useful C-4 homologating agent. Application to the synthesis of aryl iodolactones
Thibonnet, Jerome,Abarbri, Mohamed,Parrain, Jean-Luc,Duchene, Alain
, p. 7507 - 7510 (2007/10/03)
Tributylstannyl 4-tributylstannylbut-3-enoate, readily prepared by radical hydrostannation, is used for the transfer of a but-3-enoic acid synthon. Some of the potentialities of this synthon are established by the synthesis of aryl iodolactones or tetralones (one of them is a key intemediate for ABT-200 synthesis).
