379216-03-2 Usage
Functional groups
Ethyl ester, hydroxy, and oxo
Structure
Cycloheptatriene core with hydroxy groups at positions 4 and 6, and a carbonyl group at position 5
Applications
Organic synthesis, pharmaceutical research, potential pharmacological and medicinal properties
Importance
Intermediate in the production of pharmaceuticals and agrochemicals
Additional applications
Materials science, building block for complex organic molecule synthesis
Check Digit Verification of cas no
The CAS Registry Mumber 379216-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,9,2,1 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 379216-03:
(8*3)+(7*7)+(6*9)+(5*2)+(4*1)+(3*6)+(2*0)+(1*3)=162
162 % 10 = 2
So 379216-03-2 is a valid CAS Registry Number.
379216-03-2Relevant articles and documents
A new method for the synthesis of stipitatic acid isomers: Photooxygenation of ethyl 6H-cyclohepta[d][1,3]dioxole-6-carboxylate
Dastan, Arif,Saracoglu, Nurullah,Balci, Metin
, p. 3519 - 3522 (2007/10/03)
Photooxygenation of the cycloheptatriene derivative 9 gave the bicyclic endoperoxide 14. Cleavage of the peroxide linkage in 14 with thiourea resulted in the formation of 16. Treatment of the endoperoxide 14 with a catalytic amount of triethylamine provided a new isomer of stipitatic acid 11, and 16. Pyrolysis or the CoTPP (TPP = tetraphenylporphyrin) catalyzed reaction of 14 resulted in the formation of iso-stipitatic acid 10, and 18.
