101064-80-6 Usage
Chemical structure
A complex structure consisting of two 3,3-dimethylallyl groups and a 3,3-dimethylallyloxy group attached to a quinolin-2-one backbone.
Synthetic derivative
It is a synthetic derivative of quinolin-2-one, which is a heterocyclic aromatic organic compound.
Presence of functional groups
The compound contains dimethylallyl groups and an oxyfunctional group, which contribute to its unique properties.
Potential applications
Due to its unique properties, the compound may have potential applications in the fields of pharmaceuticals, materials science, and organic chemistry.
Research and study
Further research and study of this chemical may reveal its potential as a building block for new drugs or materials with specific properties.
Heterocyclic aromatic compound
It belongs to the class of heterocyclic aromatic organic compounds, which are characterized by the presence of one or more rings containing both carbon and heteroatoms (such as nitrogen, oxygen, or sulfur).
Quinolin-2-one backbone
The core structure of the compound is based on the quinolin-2-one backbone, which is a tricyclic aromatic system with a carbonyl group at the 2-position.
3,3-dimethylallyloxy group
The compound also contains a 3,3-dimethylallyloxy group, which is an oxyfunctional group that can participate in various chemical reactions and interactions.
Potential for drug development
Given its unique structure and properties, this compound may serve as a starting point for the development of new drugs targeting specific biological pathways or receptors.
Check Digit Verification of cas no
The CAS Registry Mumber 101064-80-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,6 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 101064-80:
(8*1)+(7*0)+(6*1)+(5*0)+(4*6)+(3*4)+(2*8)+(1*0)=66
66 % 10 = 6
So 101064-80-6 is a valid CAS Registry Number.
101064-80-6Relevant articles and documents
4-Hydroxycoumarin and related systems: Sitoselectivity of the Mitsunobu reaction with prenyl alcohols
Cravotto, Giancarlo,Nano, Gian Mario,Palmisano, Giovanni,Tagliapietra, Silvia
, p. 1351 - 1358 (2007/10/03)
The Mitsunobu reaction leads to the formation of new C-C bonds between prenyl alcohols and 1,3-dicarbonyl compounds like 4-hydroxycoumarin or its nitrogen isoster. Buchapine was obtained through a one-pot procedure from 4-hydroxy-2-quinolone and dimethylallyl alcohol.
A REVERSIBLE CLAISEN REARRANGEMENT OF 3-(3,3-DIMETHYLALLYL)-4-(3,3-DIMETHYLALLYLOXY)QUINOLIN-2-ONE; SYNTHESIS OF BUCHAPSINE AND LOSS OF ITS 1,1-DIMETHYLALLYL GROUP
Grundon, Michael F.,Ramachandran, V. N.
, p. 4253 - 4256 (2007/10/02)
Reversible Claisen rearrangement of 3-(3,3-dimethylallyl)-4-(3,3-dimethylallyloxy)quinolin-2-one (5) furnished the alkaloid, buchapsine (6), which readily lost the 1,1-dimethylallyl group; a mechanism for the cleavage reaction is proposed.
