140845-45-0 Usage
Chemical Class
Benzodiazepines
Explanation
1,5-Ethano-2H-1,5-benzodiazepin-3(4H)-one(9CI) belongs to the class of benzodiazepines, which are a group of psychoactive drugs that have sedative, anxiolytic, and muscle-relaxant properties.
Explanation
The molecular formula of 1,5-Ethano-2H-1,5-benzodiazepin-3(4H)-one(9CI) is C10H9N3O, indicating that it is composed of 10 carbon atoms, 9 hydrogen atoms, 3 nitrogen atoms, and 1 oxygen atom.
Explanation
1,5-Ethano-2H-1,5-benzodiazepin-3(4H)-one(9CI) is a heterocyclic compound, meaning it contains a ring of atoms with at least one heteroatom (an atom other than carbon). In this case, the compound has a diazepine ring structure, which is a six-membered nitrogen-containing ring fused to a five-membered ring.
Explanation
1,5-Ethano-2H-1,5-benzodiazepin-3(4H)-one(9CI) acts on the central nervous system by enhancing the effects of the neurotransmitter gamma-aminobutyric acid (GABA). This results in a calming and relaxing effect on the body.
Explanation
1,5-Ethano-2H-1,5-benzodiazepin-3(4H)-one(9CI) is commonly used as a medication for anxiety disorders, seizures, and insomnia due to its sedative, anxiolytic, and muscle-relaxant properties.
Structure
Heterocyclic compound with a diazepine ring
Central Nervous System (CNS) Action
Enhances the effects of GABA
Medical Uses
Anxiety disorders, seizures, and insomnia
Check Digit Verification of cas no
The CAS Registry Mumber 140845-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,8,4 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 140845-45:
(8*1)+(7*4)+(6*0)+(5*8)+(4*4)+(3*5)+(2*4)+(1*5)=120
120 % 10 = 0
So 140845-45-0 is a valid CAS Registry Number.
140845-45-0Relevant academic research and scientific papers
Doronina, S. O.,Gall', A. A.,Shishkin, G. V.
, p. 897 - 900 (1991)
Benzo-1,5-diazabicyclononen-3-one was synthesized by the oxidation of benzo-1,5-diazabicyclononen-3-ol by dimethyl sulfoxide in the presence of N,N'-dicyclohexylcarbodiimide and the reactions of this compound with 2,4-dinitrophenylhydrazine, phenylmagnesium bromide, and condensation with 4-nitrobenzaldehyde were carried out.It was shown that on heating with hydrobromic acid, benzo-1,5-diazabicyclononen-3-one undergoes dealkylation with the formation of 1,2,3,4-tetrahydroquinoxaline.