5779-99-7 Usage
Description
4-Methoxy-1,3-benzodioxole-5-carbaldehyde is an organic compound characterized by its aromatic structure and functional groups. It is a derivative of benzodioxole, featuring a methoxy group at the 4-position and a formyl group (aldehyde) at the 5-position. 4-Methoxy-1,3-benzodioxole-5-carbaldehyde is known for its chemical reactivity and potential applications in various industries due to its unique structural properties.
Uses
Used in Pharmaceutical Industry:
4-Methoxy-1,3-benzodioxole-5-carbaldehyde is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the creation of new drugs with potential therapeutic applications, making it a valuable component in the development of novel medications.
Used in Chemical Synthesis:
In the field of organic chemistry, 4-Methoxy-1,3-benzodioxole-5-carbaldehyde serves as a key intermediate for the synthesis of a wide range of chemical products. Its reactivity and functional groups enable the formation of various derivatives, which can be utilized in different applications, such as the production of specialty chemicals, dyes, and fragrances.
Used in Research and Development:
Due to its unique chemical properties, 4-Methoxy-1,3-benzodioxole-5-carbaldehyde is also used in research and development for the exploration of new chemical reactions and the discovery of novel compounds with potential applications in various industries, including pharmaceuticals, materials science, and environmental science.
Used in the Synthesis of Cotarnine Chloride:
4-Methoxy-1,3-benzodioxole-5-carbaldehyde is used as an intermediate in the synthesis of Cotarnine Chloride (C717500), which is an oxidative degradation product of the drug Noscapine (N882000). This application highlights the compound's importance in the pharmaceutical industry for the development of new drugs and drug candidates.
Check Digit Verification of cas no
The CAS Registry Mumber 5779-99-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,7 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5779-99:
(6*5)+(5*7)+(4*7)+(3*9)+(2*9)+(1*9)=147
147 % 10 = 7
So 5779-99-7 is a valid CAS Registry Number.
5779-99-7Relevant articles and documents
A new total synthesis of (±)-α-noscapine
Mao, Yongjun,Song, Shuai,Zhao, Dongmei,Cheng, Maosheng
, p. 2633 - 2640 (2014/01/06)
A new, convergent total synthesis of (±)-α-noscapine was developed on a grams scale through the condensation of 3-trimethylsilyl-meconin derivative 9 and the iodized salt cotarnine derivative 20 as the key step. Staring from simple 2,3-dimethoxybenzoic acid, piperonal and 2,2-dimethoxyethanamine, through the traditional chemical processes to give the final product in 11.6% yield over 14 steps.
Synthesis of C-1 homologues of pancratistatin and their preliminary biological evaluation
Vshyvenko, Sergey,Scattolon, Jon,Hudlicky, Tomas,Romero, Anntherese E.,Kornienko, Alexander
scheme or table, p. 4750 - 4752 (2011/09/16)
The synthesis of two C-1 analogues of pancratistatin has been accomplished in 17 steps from bromobenzene. The key steps involved the enzymatic dihydroxylation, regioselective opening of epoxyaziridine 9 with the alane derived from 8, a solid-state silica-
A convenient synthesis of 4-alkoxylated isoindolin-1-ones
Moreau, Anne,Couture, Axel,Deniau, Eric,Grandclaudon, Pierre
, p. 1664 - 1670 (2007/10/03)
A short synthesis of 4-alkoxylated isoindolin-1-ones based upon the S NAr reaction applied to phosphorylated 2-methoxybenzamides followed by alkaline cleavage of the phosphoryl auxiliary is reported.