86824-80-8 Usage
Fused Tricyclic Ring System
The compound has a unique structure with three interlocking rings, which may contribute to its potential biological activity and pharmaceutical applications.
Carbonitrile Functional Group
The presence of a carbonitrile group (C≡N) in the molecule enhances its reactivity and contributes to its potential applications in drug development.
Oxirenochromene Family
2,2-Dimethyl-2,7b-dihydro-1aH-oxireno[2,3-c]chromene-5-carbonitrile belongs to a specific family of organic compounds, which may share similar properties and potential applications.
Potential Drug Candidate
Due to its unique structure and functional groups, 2,2-Dimethyl-2,7b-dihydro-1aH-oxireno[2,3-c]chromene-5-carbonitrile is considered a potential candidate for drug development.
Versatile Compound
The compound's structure and functional groups make it suitable for various applications in the pharmaceutical industry.
Biological Activity
The molecular structure of the compound suggests that it may have biological activity, which could be harnessed in the development of new drugs for various medical conditions.
Need for Further Research
More studies and research are required to fully understand the potential uses and properties of this chemical compound, including its potential applications in drug development and the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 86824-80-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,8,2 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86824-80:
(7*8)+(6*6)+(5*8)+(4*2)+(3*4)+(2*8)+(1*0)=168
168 % 10 = 8
So 86824-80-8 is a valid CAS Registry Number.
86824-80-8Relevant academic research and scientific papers
Relaxant Activity of 4-Amido-3,4-dihydro-2H-1-benzopyran-3-ols and 4-Amido-2H-1-benzopyrans on Guinea Pig Isolated Trachealis
Buckle, Derek R.,Arch, Jonathon R. S.,Fenwick, Ashley E.,Houge-Frydrych, Catherine S. V.,Pinto, Ivan L.,et al.
, p. 3028 - 3034 (2007/10/02)
A series of 4-amido-3,4-dihydro-2H-benzopyran-3-ols and 4-amido-2H-1-benzopyrans related to the potassium channel activator cromakalim have been prepared and evaluated for their relaxant activity in guinea pig isolated tracheal spirals.Several analogues show enhanced relaxant activity relative to cromakalim in this preparation and the rank order of potency for those substituents investigated at C-6 was CF3>CN>C2H5>aza>=CH3.One compound, trans-3,4-dihydro-2,2-dimethyl-4-(2-oxopiperidin-1-yl)-7-(trifluoromethyl)-2H-1-benzopyran-3-ol (24), was resolved into its two enantiomers and the activity was shown to reside essentially in the (+)-isomer, adding further support to the suggestion that the smooth muscle receptor for these potassium channel activators is stereoselective.
