79010-31-4 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 24 carbon (C) atoms, 29 hydrogen (H) atoms, 1 nitrogen (N) atom, and 4 oxygen (O) atoms.
Explanation
Acylbenzenes are a class of chemicals that contain a benzene ring with an acyl group (a carbonyl group attached to an aromatic ring). 1-{3-acetyl-4-[3-(4-hydroxy-4-phenylpiperidin-1-yl)propoxy]phenyl}propan-1-one belongs to this class due to the presence of a benzene ring and an acetyl group.
Explanation
The compound contains an acetyl group (a carbonyl group attached to a methyl group), a propoxy group (an ether group with a three-carbon chain), and a piperidin-1-yl group (a nitrogen-containing heterocycle with a specific structure).
Explanation
The structure of the compound is described by its IUPAC name, which provides information about the arrangement of atoms and functional groups within the molecule.
Explanation
The presence of functional groups commonly found in drug molecules suggests that 1-{3-acetyl-4-[3-(4-hydroxy-4-phenylpiperidin-1-yl)propoxy]phenyl}propan-1-one may have potential pharmaceutical or medicinal applications. However, further research and testing are required to confirm its potential uses and effects.
Explanation
The compound is classified as a ketone due to the presence of a carbonyl group (C=O) bonded to two carbon-containing groups (in this case, an acetyl group and a phenyl ring).
Explanation
The compound contains a hydroxyl group (-OH) attached to a phenyl ring, which is part of the 4-phenylpiperidin-1-yl group.
Explanation
The compound contains a benzene ring, which is an aromatic ring consisting of six carbon atoms with alternating single and double bonds.
Explanation
The stereochemistry (the three-dimensional arrangement of atoms) of the compound is not specified in the provided material. Further analysis would be needed to determine the stereochemistry of the molecule.
Explanation
The solubility of the compound in various solvents is not provided in the material. Solubility can be an important factor in determining the compound's potential applications and properties.
Chemical Class
Acylbenzenes
Functional Groups
Acetyl, Propoxy, and Piperidin-1-yl
Structure
1-3-acetyl-4-[3-(4-hydroxy-4-phenylpiperidin-1-yl)propoxy]phenylpropan-1-one
Potential Applications
Pharmaceutical or Medicinal Properties
Ketone
Yes
Hydroxyl Group
Present
Aromatic Ring
Benzene
Stereochemistry
Not specified
Solubility
Not specified
Check Digit Verification of cas no
The CAS Registry Mumber 79010-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,1 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79010-31:
(7*7)+(6*9)+(5*0)+(4*1)+(3*0)+(2*3)+(1*1)=114
114 % 10 = 4
So 79010-31-4 is a valid CAS Registry Number.
79010-31-4Relevant academic research and scientific papers
1--3-substituted-aminopropanes and 2-Propanols as Potential Biodynamic Agents
Sangwan, Naresh K.,Rastogi, Shri Nivas
, p. 480 - 483 (2007/10/02)
2-Acetyl-4-(propionyl/bromo)phenols (3/4), prepared from 4-(propionyl/bromo)phenyl acetates (1/2), on alkylation with 1,3-dihalopropanes or epichlorohydrin gives the corresponding 3-halopropyl (5,6) and 2,3-epoxypropyl (7,8) ethers.Treatment of 5-8 with amines under suitable conditions yields the title compounds, 1-(2'-acetyl-4'-propionylphenoxy)-3-substituted-aminopropanes (9-11) and 1--3-substituted-amino-2-propanols (15-22).The corresponding β-pyrrolidinoethyl ethers (13,14) are prepared by alkylation of 3 and 4 with N-(β-chloroethyl)pyrrolidine.Dehydration of 10, 17 and 21 gives 12, 23 and 24, while reduction of 15 and 20 with KBH4 gives 25 and 26, respectively.Reaction of 3 and 4 with 0.5 mol of 1,3-dibromopropane and of 7 with 3 gives the corresponding 1,3-bis-aryloxypropanes (27,28) and 1,3-bis-aryloxy-2-propanol (29).Except 11 which exhibits antiinflammatory activity, no other compound shows any significant pharmacological activity.
