75267-17-3 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
5-formyl-benzo[1,3]dioxole-4-carboxylic acid ethyl ester is utilized as a building block in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the creation of diverse compounds with potential therapeutic and pesticidal properties.
Used in Organic Synthesis:
In the realm of organic synthesis, 5-formyl-benzo[1,3]dioxole-4-carboxylic acid ethyl ester serves as a reagent for the preparation of other compounds. Its functional groups facilitate various chemical reactions, contributing to the synthesis of a wide range of organic molecules.
Used in Medicinal Chemistry and Drug Discovery:
Due to its structural versatility and potential biological activity, 5-formyl-benzo[1,3]dioxole-4-carboxylic acid ethyl ester holds promise in the field of medicinal chemistry and drug discovery. Researchers can leverage its properties to develop new drugs and therapeutic agents with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 75267-17-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,6 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75267-17:
(7*7)+(6*5)+(5*2)+(4*6)+(3*7)+(2*1)+(1*7)=143
143 % 10 = 3
So 75267-17-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O5/c1-2-14-11(13)9-7(5-12)3-4-8-10(9)16-6-15-8/h3-5H,2,6H2,1H3
75267-17-3Relevant academic research and scientific papers
Total Synthesis of Decumbenine B
Xu, Xi-Yin,Qin, Guo-Wei,Xu, Ren-Sheng,Zhu, Xing-Zu
, p. 14178 - 14188 (2007/10/03)
Decumbenine B, a 3-arylisoquinoline alkaloid isolated from Corydalis decumbens, has been first synthesized from piperonal via 18 steps.The key step was condensation of 5,6-(methylenedioxy)-homophthalic anhydride 5 with Schiff base 6.
Total Synthesis of (+/-)-Chelidonine
Cushman, Mark,Choong, Tung-Chung,Valko, Joseph T.,Koleck, Mary P.
, p. 5067 - 5073 (2007/10/02)
Condensation of the Schiff base 8 with 3,4-(methylenedioxy)homophthalic anhydride (13) was exploited as the key step in a total synthesis of the benzophenanthridine alkaloid (+/-)-chelidonine (1).A variety of reaction conditions were investigated in order to maximize the production of the desired thermodynamically less stable cis diastereomer.A method was devised for the conversion of 24 to its acid chloride without production of the indenoisoquinoline 30.The migration of an aromatic ring was observed on treatment of the diazo ketone 26 with acid.This reaction is reminiscent of the Hayashi rearrangement.
