24107-34-4 Usage
Chemical Class
Benzodiazepines A class of psychoactive drugs commonly used for their sedative, hypnotic, and anxiolytic properties.
Molecular Structure
1,4-Benzodiazepine derivative This compound is derived from the 1,4-benzodiazepine structure, which is the basis for many benzodiazepine drugs.
Methyl Groups
Three methyl groups attached The compound has three methyl groups attached to the 2, 2, and 4 positions of the molecule, which may influence its potency and duration of action.
Central Nervous System Depressant
Anxiolytic, sedative, and hypnotic effects 2,2,4-Trimethyl-2,3-dihydro-1H-1,5-benzodiazepine acts as a central nervous system depressant, helping to alleviate anxiety, promote relaxation, and induce sleep.
Medical Uses
Treatment of anxiety disorders, insomnia, and epilepsy This specific benzodiazepine is prescribed to treat various conditions, including anxiety disorders, sleep disturbances, and epilepsy, due to its calming and seizure-preventing effects.
Potential for Abuse and Dependence
Risk of misuse and addiction Like other benzodiazepines, 2,2,4-Trimethyl-2,3-dihydro-1H-1,5-benzodiazepine carries a potential for abuse and dependence, which should be considered when prescribing and using the medication.
Tolerance and Withdrawal Symptoms
Long-term use may lead to tolerance and withdrawal Prolonged use of this benzodiazepine can result in the development of tolerance, requiring higher doses for the same effect, and may also cause withdrawal symptoms if discontinued abruptly.
Check Digit Verification of cas no
The CAS Registry Mumber 24107-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,1,0 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24107-34:
(7*2)+(6*4)+(5*1)+(4*0)+(3*7)+(2*3)+(1*4)=74
74 % 10 = 4
So 24107-34-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2/c1-9-8-12(2,3)14-11-7-5-4-6-10(11)13-9/h4-7,14H,8H2,1-3H3
24107-34-4Relevant articles and documents
Growth-modulating agents for the synthesis of Al-MOF-type materials based on assembled 1D structural subdomains
Moreno, José María,Velty, Alexandra,Vidal-Moya, José A.,Díaz, Urbano,Corma, Avelino
supporting information, p. 5492 - 5502 (2018/04/23)
Novel aluminium MOF-type materials structured by 1D subdomains, such as organic-inorganic nanoribbons, were synthesized by modifying the conditions of solvothermal synthesis and the nature of the solvents in the presence of aryl monocarboxylate linkers wi
1,5-benzoxazepines vs 1,5-benzodiazepines. one-pot microwave-assisted synthesis and evaluation for antioxidant activity and lipid peroxidation inhibition
Neochoritis, Constantinos G.,Tsoleridis, Constantinos A.,Stephanidou-Stephanatou, Julia,Kontogiorgis, Christos A.,Hadjipavlou-Litina, Dimitra J.
experimental part, p. 8409 - 8420 (2011/02/21)
Amino-1,5-benzoxazepines 2 and 5 and hydroxyl-1,5-benzodiazepines 3 and 6 have been synthesized in one-pot solvent-free conditions from 2,3-diaminophenol and ketones through microwave assisted acid catalysis, the benzoxazepine/ benzodiazepine ratio depend
NEW SYNTHESIS OF DIHYDRO- AND TETRAHYDRO-1,5-BENZODIAZEPINES BY REDUCTIVE CONDENSATION OF O-PHENYLENEDIAMINE AND KETONES IN THE PRESENCE OF SODIUM BOROHYDRIDE
Morales, Hilda R.,Bulbarela, Arturo,Contreras, Rosalinda
, p. 135 - 139 (2007/10/02)
Dihydro- and tetrahydro-benzodiazepines have been synthesized from o-phenylenediamine dihydrochloride and aliphatic ketones in the presence od sodium borohydride.
