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DOV 21947 hydrochloride is a chemical compound that functions as a selective serotonin and norepinephrine reuptake inhibitor (SNRI). It is recognized for its potential as an antidepressant and anxiolytic agent, with studies indicating its efficacy in treating mood and anxiety disorders, as well as attention-deficit hyperactivity disorder (ADHD). DOV 21947 hydrochloride operates by elevating the levels of serotonin and norepinephrine in the brain, which aids in mood regulation and anxiety reduction. Furthermore, it is considered to have a lower risk of side effects compared to other SNRIs, positioning it as a promising candidate for the treatment of various psychiatric conditions.

410074-74-7

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410074-74-7 Usage

Uses

Used in Pharmaceutical Industry:
DOV 21947 hydrochloride is used as an antidepressant and anxiolytic agent for the treatment of mood and anxiety disorders. It is utilized for its ability to increase serotonin and norepinephrine levels in the brain, which helps in regulating mood and reducing anxiety.
Used in Psychiatry:
DOV 21947 hydrochloride is used as a potential treatment for attention-deficit hyperactivity disorder (ADHD) due to its action as an SNRI, which may contribute to improved focus and reduced hyperactivity in affected individuals.
Used in Research and Development:
In the field of psychiatric research, DOV 21947 hydrochloride is used to explore the mechanisms of mood regulation and anxiety reduction, as well as to compare its efficacy and side effect profile with existing SNRIs, potentially leading to advancements in psychiatric treatment options.

Check Digit Verification of cas no

The CAS Registry Mumber 410074-74-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,0,0,7 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 410074-74:
(8*4)+(7*1)+(6*0)+(5*0)+(4*7)+(3*4)+(2*7)+(1*4)=97
97 % 10 = 7
So 410074-74-7 is a valid CAS Registry Number.

410074-74-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,5S)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane,hydrochloride

1.2 Other means of identification

Product number -
Other names DOV 21,947

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:410074-74-7 SDS

410074-74-7Downstream Products

410074-74-7Relevant academic research and scientific papers

USE OF AMITIFADINE, (+)-1-(3,4-DICHLOROPHENYL)-3-AZABICYCLO[3.1.0]HEXANE IN METHODS AND COMPOSITIONS WITH ENHANCED EFFICACY AND REDUCED METABOLIC SIDE EFFECTS AND TOXICITY FOR TREATMENT OF DEPRESSION AND OTHER CENTRAL NERVOUS SYSTEM DISORDERS AND CONDITIO

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, (2016/12/22)

The present invention relates to (+)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane and pharmaceutically acceptable active salts, polymorphs, glycosylated derivatives, metabolites, solvates, hydrates, and/or prodrugs of (+)-1-(3,4-dichlorophenyl)-3-azab

PREPARATION AND USE OF (+)-1-(3,4-DICHLOROPHENYL)-3-AZABICYCLO[3.1.0]HEXANE IN THE TREATMENT OF CONDITIONS AFFECTED BY MONOAMINE NEUROTRANSMITTERS

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Page/Page column 62, (2012/06/16)

The present invention relates to (+)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane and pharmaceutically acceptable active salts, polymorphs, glycosylated derivatives, metabolites, solvates, hydrates, and/or prodrugs of (+)-1-(3,4-dichlorophenyl)-3-azab

METHODS AND COMPOSITIONS FOR PRODUCTION, FORMULATION AND USE OF 1 ARYL -3-AZABICYCLO[3.1.0 ] HEXANES

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Page/Page column 37-40, (2010/11/30)

The invention provides novel compositions and methods of making (-)-1-(3,4- dichlorophenyl)-3-azabicyclo[3.1.0]hexane and other 1-aryl-3- azabicyclo[3.1.0]hexanes, including synthetic methods that form novel intermediate compounds of the invention for pro

PROCESS FOR THE SYNTHESIS OF (+) AND (-) -1-(3,4-DICHLOROPHENYL)-3-AZABICYCLO[3.1.0]HEXANE

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Page/Page column 12-13, (2008/06/13)

The present invention is concerned with novel processes for the preparation of (+)-l-(3,4- dichlorophenyl)-3-azabicyclo[3.1.0]hexane or a pharmaceutically acceptable salt thereof, and (-)- l-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane or a pharmaceutic

Novel polymorphs of azabicyclohexane

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Page/Page column 11, (2008/06/13)

The invention provides polymorphic crystalline forms of acid addition salts of (+)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane designated as polymorph form A, polymorph form B and polymorph form C, where polymorph form A is more thermodynamically stable than the other forms, methods for preparing and using such polymorph forms and pharmaceutical compositions containing such polymorph forms.

NOVEL POLYMORPHS OF AZABICYCLOHEXANE

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Page/Page column 24-26, (2008/06/13)

The invention provides polymorphic crystalline forms of acid addition salts of (+)-1-(3, 4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane designated as polymorph form A, polymorph form B and polymorph form C, where polymorph form A is more thermodynamically stable than the other forms, methods for preparing and using such polymorph forms and pharmaceutical compositions containing such polymorph forms.

(-)-1-(3,4-Dichlorophenyl)-3-azabicyclo[3.1.0]hexane, compositions thereof, and uses as a dopamine-reuptake inhibitor

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, (2008/06/13)

The present invention relates to (?)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane and pharmaceutically acceptable salts thereof, compositions comprising (?)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane or a pharmaceutically acceptable salt thereof, and methods for treating or preventing a disorder alleviated by inhibiting dopamine reuptake. In one embodiment, the disorder is attention-deficit disorder, depression, obesity, Parkinson's disease, a tic disorder, or an addictive disorder. The (?)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane or pharmaceutically acceptable salt thereof is preferably substantially free of its corresponding (+)-enantiomer.

(+)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane, compositions thereof, and uses as an anti-depressant agent

-

Example 5, (2008/06/13)

The present invention relates to (+)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane and pharmaceutically acceptable salts thereof, compositions comprising (+)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane or a pharmaceutically acceptable salt thereof, and methods for treating or preventing depression in a patient comprising administering (+)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane or a pharmaceutically acceptable salt thereof. The (+)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane or pharmaceutically acceptable salt thereof is preferably substantially free of its corresponding (?)-enantiomer.

Method of treating depression using azabicyclohexanes

-

, (2008/06/13)

The present invention concerns certain novel substituted 3-azabicyclo[3.1.0]hexanes and a method of treating depression and stress in a warm-blooded animal, comprising the administration of substituted 3-azabicyclo[3.1.0]hexanes.

Azabicyclohexanes

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, (2008/06/13)

Substituted 3-azabicyclo[3.1.0]hexanes, acid addition salts, method of use and method of preparation are described. The compounds have anxiolytic and analgesic activity.

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