93953-87-8 Usage
Class
Benzodioxepins
It belongs to a group of seven-membered rings with two oxygen atoms at positions 1 and 6.
Additional group
Methyl group
A methyl group is attached to the 2-carbon of the benzodioxepin ring.
Physical state
Colorless liquid
The compound appears as a colorless liquid at room temperature.
Molecular weight
162.185 g/mol
The molecular weight of the compound is 162.185 grams per mole.
Pharmacological properties
Potential
1,3-Benzodioxepin,4,5-dihydro-2-methyl-(9CI) has potential pharmacological properties, which may be useful in the development of pharmaceutical drugs.
Specific uses and effects
Not well-studied or documented
The specific uses and effects of this compound have not been extensively researched or documented in the scientific literature.
Check Digit Verification of cas no
The CAS Registry Mumber 93953-87-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,5 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93953-87:
(7*9)+(6*3)+(5*9)+(4*5)+(3*3)+(2*8)+(1*7)=178
178 % 10 = 8
So 93953-87-8 is a valid CAS Registry Number.
93953-87-8Relevant articles and documents
Conformational consequence of stereoelectronic effects in seven-membered cyclic acetals: nuclear magnetic resonance invastigation of 1,3-benzodioxepin and its 2-substituted derivatives
St-Amour, Robert,Viet, M. T. Phan,St-Jacques, Maurice
, p. 2830 - 2840 (2007/10/02)
The conformational and dynamic properties of 1,3-dioxa-4,5-benzocycloheptene (8) and several 2-substituted derivatives were investigated by 1H and 13C low temperature nmr methods.The results are strikingly different from those reported for the analogous symmetrical dioxepin isomers derived from 2.The unexpectedly large preference of the 2-methoxy derivative (8c) for the Ce conformation is explained in terms of deformed torsional angles in the seven-membered ring relative to those in the analogous six-membered one.These results therefore help delineate the limitations to the conformational biasing normally associated with the anomeric effect.
