36129-37-0 Usage
Molecular structure
2-(5-propyldihydrofuran-2(3H)-ylidene)cyclopentane-1,3-dione has a complex molecular structure, featuring a cyclopentane ring, a dihydrofuran ring, and various substituents.
Cyclopentane ring
The compound contains a five-carbon cyclic structure, which is a type of cycloalkane.
Dihydrofuran-2(3H)-ylidene group
A five-membered dihydrofuran ring with a ylidene group (R2C=CR) attached to the carbon at position 2 of the cyclopentane ring.
Propyl group
A three-carbon alkyl chain (CH3-CH2-CH2-) is attached to the dihydrofuran-2(3H)-ylidene group, forming a 5-propyldihydrofuran-2(3H)-ylidene moiety.
Potential applications
Due to its unique structure, 2-(5-propyldihydrofuran-2(3H)-ylidene)cyclopentane-1,3-dione may have potential applications in the pharmaceutical or chemical industries, although further research and testing are required to determine specific uses.
Investigation needed
The specific properties and potential uses of 2-(5-propyldihydrofuran-2(3H)-ylidene)cyclopentane-1,3-dione are not yet fully understood and require further investigation through research and testing.
Check Digit Verification of cas no
The CAS Registry Mumber 36129-37-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,2 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 36129-37:
(7*3)+(6*6)+(5*1)+(4*2)+(3*9)+(2*3)+(1*7)=110
110 % 10 = 0
So 36129-37-0 is a valid CAS Registry Number.
36129-37-0Relevant academic research and scientific papers
Oxonium Ion Elektrophiles: Synthesis of the Hypotensive Oudenone.
Bates, Hans, Aaron,Farina, James
, p. 3843 - 3845 (2007/10/02)
The hypotensive oudenone (1) has been synthesized through the intermediacy of oxonium ion 4.Acid-catalyzed C-alkylation of 1,3-cyclopentanedione (3) with 5-propyltetrahydro-2-furanol (6b) afforded dihydrooudenone 2b.In contrast, alkylation of 3 with 2-chloro-5-propyltetrahydrofuran (7b) was unsuccessful.Unsaturation was introduced into 2b by treatment with N-(phenylthio)succinimide to produce 10 followed by oxidation to the corresponding sulfoxide and elimination of phenylsulfenic acid, which produced oudenone(1).
