184360-97-2 Usage
General Description
2,3-(Methylenedioxy)benzaldehyde is a chemical compound with the molecular formula C8H6O3. It is a pale yellow liquid with a sweet, floral odor, commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. The compound is also known for its presence in natural sources such as vanilla and cinnamon. It is widely utilized in the production of fragrances, flavorings, and as a precursor for a variety of chemical reactions. Additionally, 2,3-(Methylenedioxy)benzaldehyde has been studied for its potential pharmacological properties and therapeutic applications, including its role as an antifungal and antibacterial agent. However, it is important to note that the compound should be handled with care due to its potential irritant properties.
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 articles and documents
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.
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).
