3041-17-6 Usage
Cyclic Compound
Yes
Explanation
1-Benzoxepin-2(3H)-one, 4,5-dihydrois a cyclic compound, meaning its atoms are arranged in a closed loop or ring.
Explanation
The cyclic structure of this compound consists of a six-membered ring, which includes both carbon and oxygen atoms.
Explanation
The compound contains both oxygen and carbon atoms in its structure, contributing to its unique properties and potential applications.
Explanation
Studies have shown that 1-Benzoxepin-2(3H)-one, 4,5-dihydrohas antiproliferative and anticancer properties, making it a candidate for further research and development in the pharmaceutical industry.
Explanation
Due to its unique structure, this compound can be used as a building block in the synthesis of other organic compounds, potentially leading to the development of novel compounds with various applications.
Explanation
The specific industrial applications of 1-Benzoxepin-2(3H)-one, 4,5-dihydromay vary depending on its specific properties and the context in which it is used. Further research and development could reveal new industrial uses for this compound.
Explanation
The properties and uses of 1-Benzoxepin-2(3H)-one, 4,5-dihydrocan differ based on the specific application and context in which it is employed. This means that its potential benefits and limitations may change depending on the situation.
Ring Size
Six-membered
Oxygen and Carbon Atoms
Present
Potential Pharmaceutical Applications
Yes
Building Block in Organic Synthesis
Yes
Industrial Applications
Potential
Specific Properties and Uses
Vary by Application
Check Digit Verification of cas no
The CAS Registry Mumber 3041-17-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,4 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3041-17:
(6*3)+(5*0)+(4*4)+(3*1)+(2*1)+(1*7)=46
46 % 10 = 6
So 3041-17-6 is a valid CAS Registry Number.
3041-17-6Relevant articles and documents
PdI2-catalyzed regioselective cyclocarbonylation of 2-allyl phenols to dihydrocoumarins
Amzquita-Valencia, Manuel,Alper, Howard
, p. 5827 - 5829 (2015/01/08)
A simple, efficient, and regioselective synthesis of 3-methyl-3,4-dihydrocoumarins is reported. The reaction of 2-allyl phenols with synthesis gas was catalyzed by PdI2, and 1,3,5,7-tetramethyl-6-phenyl-2,4,8-trioxa-6-phosphaadamantane (L1) and 1,3,5,7-tetramethyl-6-tetradecyl-2,4,8-trioxa-6-phosphaadamantane (L2) were effective as ligands, affording good product selectivity in all cases.
Lactone formation by rhodium-catalyzed C-C bond cleavage of cyclobutanone
Murakami, Masahiro,Tsuruta, Takuo,Ito, Yoshihiko
, p. 2484 - 2486 (2007/10/03)
As a coordinating ligand, the phenol group in appropriately substituted cyclobutanones facilitates the Rh1-catalyzed activation of the C-C bond between the carbonyl group and the α-carbon atom. This novel reaction leads, depending on the position of the phenol group on the cyclobutanone ring, to lactones of varying ring size (for example, as shown for a seven-membered-ring lactone).