92582-15-5 Usage
Molecular Structure
2-(5-acetyl-2,3-dihydro-1-benzofuran-2-yl)propan-2-yl acetate consists of a benzofuran ring with an acetyl group at the 5th position and a propan-2-yl acetate group at the 2nd position.
Complexity
The compound has a complex structure due to the presence of multiple functional groups and a heterocyclic ring.
Molecular Weight
The molecular weight of 2-(5-acetyl-2,3-dihydro-1-benzofuran-2-yl)propan-2-yl acetate is 250.29 g/mol.
Potential Applications
2-(5-acetyl-2,3-dihydro-1-benzofuran-2-yl)propan-2-yl acetate has potential applications in the pharmaceutical and chemical industries, although further studies and research are needed to determine its precise properties and uses.
Stability
The stability of 2-(5-acetyl-2,3-dihydro-1-benzofuran-2-yl)propan-2-yl acetate is not explicitly mentioned, but it is generally expected to be stable under normal conditions for organic compounds.
Solubility
The solubility of 2-(5-acetyl-2,3-dihydro-1-benzofuran-2-yl)propan-2-yl acetate is not provided, but it is likely to be soluble in organic solvents such as ethanol, acetone, or dichloromethane, and insoluble in water due to its nonpolar nature.
Reactivity
The reactivity of 2-(5-acetyl-2,3-dihydro-1-benzofuran-2-yl)propan-2-yl acetate may vary depending on the specific reaction conditions and the presence of other reactive groups in the molecule.
Synthesis
The synthesis of 2-(5-acetyl-2,3-dihydro-1-benzofuran-2-yl)propan-2-yl acetate may involve multiple steps, including the formation of the benzofuran ring, the introduction of the acetyl group at the 5th position, and the attachment of the propan-2-yl acetate group at the 2nd position.
Further Research
The properties and potential uses of 2-(5-acetyl-2,3-dihydro-1-benzofuran-2-yl)propan-2-yl acetate are not yet fully understood and require additional studies and research to determine its potential applications and limitations.
Check Digit Verification of cas no
The CAS Registry Mumber 92582-15-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,8 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92582-15:
(7*9)+(6*2)+(5*5)+(4*8)+(3*2)+(2*1)+(1*5)=145
145 % 10 = 5
So 92582-15-5 is a valid CAS Registry Number.
92582-15-5Relevant academic research and scientific papers
cis-Oxypalladation Complexes Derived from (1R,5R)-2(10),3-Pinadiene and Their Utilization in Pd(II)-catalyzed Enantioselective Cyclization of 2-(trans-2-Butenyl)phenols
Hosokawa, Takahiro,Imada, Yasushi,Murahashi, Shun-Ichi
, p. 3282 - 3290 (2007/10/02)
(1R,5R)-2(10),3-Pinadiene, when treated with either Na2PdCl4 in MeOH or Pd(OAc)2 in AcOH and NaCl, gives di-μ-chloro-bis (4a) or (4b), respectively.These complexes represent the firstly isolated cis-oxypalladation adduct.The ligand exchange of 4b with AgOAc affords di-μ-acetato-bis (5b) which serves as the catalyst for the asymmetric cyclization of 2-(trans-2-butenyl)phenols leading to 2-vinyl-2,3-dihydrobenzofurans (13).Although the enantioselectivities induced in this asymmetric cyclization are not high (1-29percent ee), noteworthy is that the cis-complex 5b affords (R)-(-)-enantiomer of 13 while the parent di-μ-acetato-bis give the (S)-isomer.As an application of the present asymmetric cyclization, attempts to synthesize (S)-(+)-tremetone have been made.
