Interesting facts
Interesting Facts about 7-chloro-4-hydroxy-N-methyl-5-phenyl-3H-1,4-benzodiazepin-2-imine
The compound known as 7-chloro-4-hydroxy-N-methyl-5-phenyl-3H-1,4-benzodiazepin-2-imine is a fascinating member of the benzodiazepine family, which are well-known for their variety of effects on the central nervous system. Here are some notable aspects of this compound:
- Pharmacological Interest: This compound, like other benzodiazepines, may exhibit anxiolytic (anxiety-reducing), sedative, and muscle-relaxing properties, making it a target for research in developing new therapies.
- Synthesis: The synthesis of such complex benzodiazepine derivatives typically involves multiple steps, showcasing the creativity of organic chemists in designing specific structures that influence biological activity.
- Structure-Activity Relationship: The specific substitutions on the benzodiazepine core greatly affect the pharmacological properties. For example, the presence of the 7-chlorine and 4-hydroxyl groups can alter the binding affinity at the GABAA receptor, which is crucial for the compound's potential therapeutic effects.
- Research Applications: Compounds like this are often studied in academic and clinical settings for understanding their mechanisms of action, toxicity, and overall therapeutic potential, especially in the context of mental health disorders.
- Historical Context: The benzodiazepine class emerged in the 1960s, revolutionizing the treatment of anxiety and insomnia, with many early examples still in use today.
As noted by experts in the field, "the strategic modification of benzodiazepine structures has led to some of the most effective drugs in psychopharmacology." This emphasizes the importance of continued research on compounds like 7-chloro-4-hydroxy-N-methyl-5-phenyl-3H-1,4-benzodiazepin-2-imine in the quest for better mental health solutions.
Synonyms
chlordiazepoxide
58-25-3
Methaminodiazepoxide
Librium
Chlozepid
Librelease
Libritabs
Elenium
Chlorodiazepoxide
Clopoxide
Helogaphen
Silibrin
Multum
Radepur
Risolid
Tropium
Sonimen
Zeisin
Chlordiazepoxidum
Clordiazepoxido
Lygen
Chloradiazepoxide
Balance (pharmaceutical)
3H-1,4-Benzodiazepin-2-amine, 7-chloro-N-methyl-5-phenyl-, 4-oxide
Chlordiazepoxidum [INN-Latin]
Clordiazepoxido [INN-Spanish]
7-Chloro-N-methyl-5-phenyl-3H-1,4-benzodiazepin-2-amine 4-oxide
Libritabs (TN)
Chlordiazepoxide civ
7-chloro-4-hydroxy-N-methyl-5-phenyl-3H-1,4-benzodiazepin-2-imine
HSDB 3028
6RZ6XEZ3CR
EINECS 200-371-0
Chlordiazepoxid
Chloridiazepide
Kalmocaps
Viopsicol
Control
Decacil
Ifibrium
Librinin
Menrium
Mesural
Mildmen
Napoton
Psicosan
Zetran
CHEMBL451
Chlordiazepoxide [USP:INN:BAN:JAN]
7-Chloro-2-(methylamino)-5-phenyl-3H-1,4-benzodiazepine 4-oxide
7-Chlor-2-methylamino-5-phenyl-3H-1,4-benzodiazepin-4-oxid [German]
CHLORDIAZEPOXIDE [MI]
CHLORDIAZEPOXIDE [INN]
CHLORDIAZEPOXIDE [JAN]
CHLORDIAZEPOXIDE [HSDB]
CHEBI:3611
CHLORDIAZEPOXIDE [VANDF]
CHLORDIAZEPOXIDE [MART.]
Disarim
DTXCID2026022
DTXSID4046022
7-Chlor-2-methylamino-5-phenyl-3H-1,4-benzodiazepin-4-oxid
Clordiazepossido
CHLORDIAZEPOXIDE [WHO-DD]
Eden-psich
Chlordiazepoxydum
3H-1,4-Benzodiazepine, 7-chloro-2-(methylamino)-5-phenyl-, 4-oxide
CHLORDIAZEPOXIDE CIV [USP-RS]
CHLORDIAZEPOXIDE [ORANGE BOOK]
CHLORDIAZEPOXIDE [EP MONOGRAPH]
CHLORDIAZEPOXIDE [USP MONOGRAPH]
MENRIUM COMPONENT CHLORDIAZEPOXIDE
Chlordiazepoxide Base
LIMBITROL COMPONENT CHLORDIAZEPOXIDE
7-Chloro-2-methylamino-5-phenyl-3H-1,4-benzodiazepin-4-oxide
7-Chloro-2-methylamino-5-phenyl-3H-1,4-benzodiazepine-4-oxide
LIMBITROL DS COMPONENT CHLORDIAZEPOXIDE
Clordiazepossido [Italian]
Chlordiazepoxidum (INN-Latin)
Clordiazepoxido (INN-Spanish)
CHLORDIAZEPOXIDE (MART.)
CHLORDIAZEPOXIDE CIV (USP-RS)
7-chloro-2-(methylamino)-5-phenyl-3H-1,4-benzodiazepin-4-ium-4-olate
Chlordiazepoxide (USP:INN:BAN:JAN)
CHLORDIAZEPOXIDE (EP MONOGRAPH)
CAS-58-25-3
CHLORDIAZEPOXIDE (USP MONOGRAPH)
SMR000469226
Chlordiazepoxide (1.0 mg/mL in Methanol)
UNII-6RZ6XEZ3CR
Angirex
Klopoxid
Sarlib
Metaminodiazepoxide
chlordiazepoxide-hcl
7-Cloro-2-metilamino-5-fenil-3H-1,4-benzodiazepina 4-ossido [Italian]
Chlordiazep-oxide HCl
7-Cloro-2-metilamino-5-fenil-3H-1,4-benzodiazepina 4-ossido
Spectrum2_001157
Spectrum4_000578
Spectrum5_001623
3H-1,4-Benzodiazepin-2-amine, 7-chloro-N-methyl-5-phenyl, 4-oxide
SCHEMBL18474
KBioGR_001016
MLS001066622
MLS001424220
MLS003899195
DivK1c_000995
SCHEMBL145243
SPBio_001113
LIBRIUM /HYDROCHLORIDE/
GTPL3370
CHEBI:94781
HMS503G11
KBio1_000995
DTXSID40861935
N05BA02
ANTSCNMPPGJYLG-UHFFFAOYSA-N
BUCORZSTKDOEKQ-UHFFFAOYSA-N
NINDS_000995
HMS2052C19
HMS2231M10
HMS3373M10
HMS3394C19
7 Chloro 2 methylamino 5 phenyl 3H 1,4 benzodiazepine 4 oxide
7-Chloro-2-methylamino-5-phenyl-3H-1,4-benzodiazepine 4-oxide
Chlordiazepoxide (JP18/USP/INN)
Tox21_111567
Tox21_111568
3H-1,4-benzodiazepin-2-amine,7-chloro-N-methyl-5-phenyl-,4-oxide
7 Chloro N methyl 5 phenyl 3H 1,4 benzodiazepin 2 amine 4 oxide
BBL010791
BDBM50007664
STK597142
AKOS005518509
AKOS015963131
AB06298
CCG-101136
DB00475
NC00386
Chlordiazepoxide 1.0 mg/ml in Methanol
IDI1_000995
Chlordiazepoxide, 1mg/ml in Acetonitrile
NCGC00246347-01
AC-13012
VS-02683
CHLORDIAZEPOXIDE COMPONENT OF MENRIUM
DB-053173
NS00000042
CHLORDIAZEPOXIDE COMPONENT OF LIMBITROL
D00267
AB00053219-06
CHLORDIAZEPOXIDE COMPONENT OF LIMBITROL DS
Q178566
W-105404
7-chloro-2-(methylamino)-5-phenyl-3H-1,4lambda5-benzodiazepin-4-one
7-Chloro-2-(methylimino)-5-phenyl-2,3-dihydro-4H-1,4-benzodiazepin-4-ol
7-Chloro-N-methyl-5-phenyl-3H-1,4-benzodiazepin-2amine-4-oxide; Clopoxide
(1E,4E)-7-chloro-2-(methylamino)-5-phenyl-3H-benzo[e][1,4]diazepine 4-oxide
200-371-0
Solubility of 7-chloro-4-hydroxy-N-methyl-5-phenyl-3H-1,4-benzodiazepin-2-imine (C16H12ClN3O)
The solubility characteristics of 7-chloro-4-hydroxy-N-methyl-5-phenyl-3H-1,4-benzodiazepin-2-imine can be quite intriguing due to its complex structure. This compound contains multiple functional groups that significantly influence its interaction with solvents.
Factors Affecting Solubility
It is essential to consider that the solubility tends to be:
As a result, one may conclude that while this compound maintains significant solubility in certain organic solvents, its solubility in water is relatively low due to the competition between its polar and non-polar characteristics. Solubility testing in different solvents would provide further insights into its behavior under various conditions.