133662-07-4 Usage
1-Piperidineacetic acid, alpha-oxo-, (1-(2-chlorophenyl)ethylidene)hydrazide, (E)(Clonitrazepam) properties and specific content
A chemical compound consisting of 15 carbon atoms, 18 hydrogen atoms, 1 chlorine atom, 3 nitrogen atoms, and 2 oxygen atoms.
2. Potent and long-acting benzodiazepine derivative
A powerful medication that belongs to the benzodiazepine class, known for its long-lasting effects.
3. Treatment of chronic anxiety disorders
Used for managing conditions such as panic disorder and other chronic anxiety-related issues.
Mechanism of action
Enhances the effects of GABA
The medication works by increasing the impact of gamma-aminobutyric acid (GABA), a natural chemical in the body that helps to calm the nervous system.
5. Short-term relief of severe or disabling anxiety
Clonitrazepam is typically prescribed for a temporary period to alleviate intense or incapacitating anxiety symptoms, rather than for everyday stress.
6. Available in tablet form
The medication is commonly found in tablet form, which should be taken as directed by a healthcare professional.
Side effects
Drowsiness, dizziness, headache
Some common side effects of Clonitrazepam may include excessive tiredness, lightheadedness, and head pain.
Consultation with a doctor
Discuss potential side effects or concerns
It is crucial to consult a healthcare professional and discuss any possible side effects or concerns before starting treatment with Clonitrazepam.
Check Digit Verification of cas no
The CAS Registry Mumber 133662-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,6,6 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 133662-07:
(8*1)+(7*3)+(6*3)+(5*6)+(4*6)+(3*2)+(2*0)+(1*7)=114
114 % 10 = 4
So 133662-07-4 is a valid CAS Registry Number.
133662-07-4Relevant academic research and scientific papers
Galons,Cave,Miocque,Rinjard,Tran,Binet
, p. 785 - 788 (1990)
A series of acylated hydrazones: o-Cl-C6H4-C(R1) = N-NH-CO-R, have been prepared and evaluated on spontaneous hypertensive rats (SHR). The more active compounds present a hydroxyl in position α to the acyl group and R
