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5H-dibenzo[a,d]cyclohepten-5-one O-[2-(methylamino)ethyl]oxime monohydrochloride is a complex organic compound with a unique chemical structure. It is characterized by its tricyclic nature and the presence of an oxime group, which contributes to its potential applications in various fields.

18059-99-9

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18059-99-9 Usage

Uses

Used in Pharmaceutical Industry:
5H-dibenzo[a,d]cyclohepten-5-one O-[2-(methylamino)ethyl]oxime monohydrochloride is used as a tricyclic antidepressant for the treatment of major depressive disorder. Its chemical structure allows it to interact with specific receptors in the brain, modulating the levels of neurotransmitters and providing relief from depressive symptoms.
Used in Antibacterial Applications:
In the field of antibacterial research, 5H-dibenzo[a,d]cyclohepten-5-one O-[2-(methylamino)ethyl]oxime monohydrochloride serves as a potential new agent. Its unique chemical properties may enable it to target bacterial cells in novel ways, offering an alternative to existing antibiotics and potentially overcoming issues of antibiotic resistance.
Used in Drug Delivery Systems:
Similar to gallotannin, 5H-dibenzo[a,d]cyclohepten-5-one O-[2-(methylamino)ethyl]oxime monohydrochloride may also benefit from advancements in drug delivery systems. By employing carriers such as organic and metallic nanoparticles, the compound's delivery, bioavailability, and therapeutic outcomes could be improved, enhancing its effectiveness in various applications.

Originator

Deparon,Aron,France,1981

Manufacturing Process

1.15 g of Na are dissolved in 100 ml of absolute ethanol; 10 g of 5-oximino5H-dibenzo[a,d]cycloheptene are introduced, followed by boiling under reflux for 1 hour and evaporation to dryness. The residue is dissolved in dimethylformamide and part of the solvent is distilled off. The solution is now cooled to about 20°C and there are added 5.3 g of methylaminoethyl chloride which is prepared below 10°C from the corresponding hydrochloride by supersaturation with potassium carbonate. The mixture is then heated to 100°C for 1? hours. Finally, the mixture is evaporated to dryness, the residue dissolved in ether/water and the ethereal phase washed with water. After drying of the ethereal phase with potassium carbonate, 8.5 g of the hydrochloride of 5-β-methylaminoethoxyimino-5H-dibenzo[a,d]cycloheptene (melting point 232°C to 233°C) are obtained.

Therapeutic Function

Antidepressant

Check Digit Verification of cas no

The CAS Registry Mumber 18059-99-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,5 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18059-99:
(7*1)+(6*8)+(5*0)+(4*5)+(3*9)+(2*9)+(1*9)=129
129 % 10 = 9
So 18059-99-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H18N2O.ClH/c1-19-12-13-21-20-18-16-8-4-2-6-14(16)10-11-15-7-3-5-9-17(15)18;/h2-11,19H,12-13H2,1H3;1H

18059-99-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(dibenzo[1,2-a:1',2'-e][7]annulen-11-ylideneamino)oxyethyl-methylazanium,chloride

1.2 Other means of identification

Product number -
Other names LM 2909

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:18059-99-9 SDS

18059-99-9Upstream product

18059-99-9Downstream Products

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