CAS 846-49-1
:2H-1,4-Benzodiazepin-2-one, 7-chloro-5-(2-chlorophenyl)-1,3-dihydro-3-hydroxy-
Description:
The chemical substance known as 2H-1,4-Benzodiazepin-2-one, 7-chloro-5-(2-chlorophenyl)-1,3-dihydro-3-hydroxy- (CAS number 846-49-1) is a member of the benzodiazepine family, which is characterized by a fused benzene and diazepine ring structure. This compound typically exhibits psychoactive properties, often functioning as a central nervous system depressant. Its structure includes a chloro substituent at the 7-position and a 2-chlorophenyl group at the 5-position, which can influence its pharmacological activity and potency. The presence of a hydroxy group at the 3-position contributes to its chemical reactivity and potential interactions with biological targets. Benzodiazepines are commonly used for their anxiolytic, sedative, and muscle relaxant effects, although they may also pose risks of dependence and withdrawal. The specific characteristics, such as solubility, melting point, and stability, can vary based on the compound's formulation and purity. As with all chemical substances, proper handling and safety precautions are essential due to potential toxicity and regulatory considerations.
Formula:C15H10Cl2N2O2
InChI:InChI=1/C15H10Cl2N2O2/c16-8-5-6-12-10(7-8)13(19-15(21)14(20)18-12)9-3-1-2-4-11(9)17/h1-7,15,21H,(H,18,20)
InChI key:InChIKey=DIWRORZWFLOCLC-UHFFFAOYSA-N
SMILES:ClC1=C(C=2C=3C(NC(=O)C(O)N2)=CC=C(Cl)C3)C=CC=C1
Synonyms:- (.+-.)-Lorazepam
- (RS)-Lorazepam
- 2H-1,4-Benzodiazepin-2-one, 7-chloro-5-(o-chlorophenyl)-1,3-dihydro-3-hydroxy-
- 7-Chloro-5-(2-chlorophenyl)-1,3-dihydro-3-hydroxy-2H-1,4-benzodiazepin-2-one
- 7-Chloro-5-(2-chlorophenyl)-3-hydroxy-1H-1,4-benzodiazepin-2(3H)-one
- 7-Chloro-5-(o-chlorophenyl)-1,3-dihydro-3-hydroxy-2H-1,4-benzodiazepin-2-one
- Almazine
- Anxiedin
- Anxira
- Anzepam
- Aplacasse
- Aplacassee
- Apo-Lorazepam
- Aripax
- Ativan
- Azurogen
- Bonatranquan
- Bonton
- Control
- Delormetazepam
- Demethyllormetazepam
- Duralozam
- Efasedan
- Emotival
- Equitam
- Kalmalin
- Larpose
- Laubeel
- Lopam
- Lorabenz
- Loram
- Lorans
- Lorapam
- Lorat
- Lorax
- Lorazem
- Lorazene
- Lorazep
- Lorazin
- Lorazon
- Lorenin
- Loridem
- Lorivan
- Lorsedal
- Lorsilan
- Lorzem
- Lozepam
- Merlit
- NIC
- Nervistop L
- Norlormetazepam
- Novhepar
- Novo-lorazem
- Nsc 289758
- Orfidal
- Pro Dorm
- Psicopax
- Punktyl
- Quait
- Renaquil
- Reposepan
- Rocosgen
- Securit
- Sedatival
- Sedazin
- Sedizepan
- Sidenar
- Silence
- Sinestron
- Somagerol
- Stapam
- Tavor
- Tavor Expidet
- Temesta
- Titus
- Tranqipam
- Trapax
- Trapex
- Upan
- Wintin
- Wy 4036
- Wypax
- o-Chlorooxazepam
- o-Chloroxazepam
- 2H-1,4-Benzodiazepin-2-one, 7-chloro-5-(2-chlorophenyl)-1,3-dihydro-3-hydroxy-
- (+-)-lorazepam--dea schedule iv item
- 1,4-benzodiazepin-2-one,7-chloro-5-(o-chlorophenyl)-1,3-dihydro-3-hydroxy-2
- AURORA KA-7219
- 7-Chloro-5-(2-chlorophenyl)-3-hydroxy-1,3-dihydro-2H-1,4-benzodiazepin-2-one
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Found 15 products.
Lorazepam
CAS:Controlled Product<p>Impurity Lorazepam USP Related Compound A<br>Stability hygroscopic<br>Applications Lorazepam is an anxiolytic compound that potentiates GABAergic synaptic transmission by binding at the benzodiazepine site on the GABAA receptor.1,2 This product is intended for forensic and research applications. Lorazepam acts as ananticonvulsant. Lorazepam USP Related Compound A.Controlled substance (depressant).<br>References Rutgers, G., et al.: Anal. Profiles Drug Subs., 9, 397 (1980), Korkmaz, S., et al.: Eur. Neuropsychopharmacol., 8, 175 (1998), D’Onofrio, G., et al.: N. Engl. J. Med., 340, 915 (1999),<br></p>Formula:C15H10Cl2N2O2Color and Shape:NeatMolecular weight:321.16Lorazepam
CAS:Controlled Product<p>Lorazepam is a benzodiazepine that binds to the benzodiazepine receptor in the central nervous system. This binding induces a variety of effects, including sedation, muscle relaxation, and suppression of anxiety. Lorazepam can be used as an antianxiety agent and as an adjunct to anesthesia. Lorazepam is metabolized by oxidation at the 3-position to produce lorazepam-3-glucuronide (LZG), which is excreted in urine. The major metabolic pathway involves glucuronidation followed by biliary excretion of LZG. Benzalkonium chloride has been used for analytical purposes in chromatographic analysis with minimal toxicity.</p>Formula:C15H10Cl2N2O2Purity:Min. 95%Color and Shape:Slightly Yellow PowderMolecular weight:321.16 g/molLORAZEPAM FOR SYSTEM SUITABILITY CRS - * PSY (LORAZEPAM)
CAS:Controlled Product<p>LORAZEPAM FOR SYSTEM SUITABILITY CRS - * PSY (LORAZEPAM)</p>Formula:C15H10Cl2N2O2Molecular weight:321.1581LORAZEPAM CRS - * PSY
CAS:Controlled Product<p>LORAZEPAM CRS - * PSY</p>Formula:C15H10Cl2N2O2Color and Shape:Crystalline Powder. White. Powder.Molecular weight:321.1581Lorazepam
CAS:Controlled ProductLorazepamFormula:C15H10Cl2N2O2Purity:99.7%Color and Shape:White CrystallineMolecular weight:320.01193Lorazepam (100 μg/mL in Acetonitrile)
CAS:Controlled ProductFormula:C15H10Cl2N2O2Color and Shape:Single SolutionMolecular weight:321.16Lorazepam (1.0 mg/mL in Acetonitrile)
CAS:Controlled ProductFormula:C15H10Cl2N2O2Color and Shape:Single SolutionMolecular weight:321.16Lorazepam CIV
CAS:Controlled Product<p>Alprazolam(inn), camazepam (inn), chlordiazepoxide (inn), clonazepam (inn), clorazepate & other heterocyclic compounds with nitro atom(s) only</p>Formula:C15H10Cl2N2O2Color and Shape:White Off-White Crystalline PowderMolecular weight:320.01193N-Nitroso Lorazepam
CAS:Controlled Product<p>Applications N-Nitroso Lorazepam is an impurity of Lorazepam (L469850), which is an anxiolytic compound that potentiates GABAergic synaptic transmission by binding at the benzodiazepine site on the GABAA receptor.1,2 This product is intended for forensic and research applications. Lorazepam acts as ananticonvulsant.<br>References Rutgers, G., et al.: Anal. Profiles Drug Subs., 9, 397 (1980), Korkmaz, S., et al.: Eur. Neuropsychopharmacol., 8, 175 (1998), D’Onofrio, G., et al.: N. Engl. J. Med., 340, 915 (1999),<br></p>Formula:C15H9Cl2N3O3Color and Shape:NeatMolecular weight:350.16







