91301-42-7 Usage
Chemical Structure
1,3-Cyclohexanedione with a benzoyloxyphenylmethylene group and two methyl groups attached
Explanation
The chemical structure describes the arrangement of atoms in the molecule. This compound has a cyclohexanedione ring (six-membered ring with two carbonyl groups at positions 1 and 3) with a benzoyloxyphenylmethylene group and two methyl groups attached to it.
Explanation
The compound is derived from cyclohexanedione, which is a six-membered ring with two carbonyl groups. The additional functional groups in this compound differentiate it from the parent compound.
Explanation
This compound is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds due to its unique structure and reactivity.
Explanation
The compound contains several functional groups, including a benzoyloxyphenylmethylene group (an aromatic group with a benzoyloxy and phenylmethylene attached), two methyl groups (CH3), and two carbonyl groups (C=O) within the cyclohexanedione ring.
Explanation
Most organic compounds with molecular weights around 300-400 g/mol, like this one, are solids at room temperature due to their relatively large size and the presence of multiple functional groups that can form intermolecular interactions.
Explanation
The compound is likely soluble in organic solvents due to its nonpolar nature and the presence of aromatic rings and aliphatic groups. However, it may not be soluble in water due to the lack of polar functional groups.
Explanation
The compound is expected to be stable under normal conditions, such as room temperature and atmospheric pressure, as it does not contain any highly reactive functional groups.
Explanation
The compound's carbonyl groups and aromatic rings make it susceptible to reactions with nucleophiles (like amines, alcohols, and hydrides) and electrophiles (like halogens and other electrophilic reagents), which can be useful in the synthesis of various organic compounds and pharmaceuticals.
Derivative of Cyclohexanedione
Yes
Application
Synthesis of pharmaceuticals and other organic compounds
Field of Relevance
Organic Chemistry and Drug Development
Functional Groups
Benzoyloxyphenylmethylene, Methyl groups, and Carbonyl groups
Physical State
Likely a solid at room temperature
Solubility
Soluble in organic solvents like dichloromethane, ethyl acetate, and acetone
Stability
Stable under normal conditions
Reactivity
Reactive towards nucleophiles and electrophiles
Check Digit Verification of cas no
The CAS Registry Mumber 91301-42-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,0 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 91301-42:
(7*9)+(6*1)+(5*3)+(4*0)+(3*1)+(2*4)+(1*2)=97
97 % 10 = 7
So 91301-42-7 is a valid CAS Registry Number.
91301-42-7Relevant articles and documents
The Reaction of Cyclic 1,3-Diketones with Alkylcyclopropenium Ions to Yield 2-Alkyltihio-substituted 2H-Pyrans
Yoshida, Hiroshi,Nakajima, Mikito,Ogata, Tsuyoshi,Matsumoto, Kiyoshi
, p. 734 - 738 (2007/10/02)
This study treats the reactions of methylthio-, ethylthio-, or benzylthiodiphenylcyclopropenium ion(1) with 5-, 6-, and 7-membered cyclic 1,3-diketones, giving either 2-alkylthio-2H-pyrans or dienone derivatives.Treatment of 1 with 1,3-cyclopentanedione,
