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1-aMino-3-Methyl-4,5-dihydro-1H-benzo[d]azepin-2(3H)-one is a heterocyclic organic molecule belonging to the benzoazepine class, characterized by the presence of an amino group, a methyl group, and a carbonyl group within its complex molecular structure. 1-aMino-3-Methyl-4,5-dihydro-1H-benzo[d]azepin-2(3H)-one is utilized in pharmaceutical research and drug development, and it may hold potential for the treatment of central nervous system disorders or psychiatric conditions due to its unique chemical structure and pharmacological properties. Further research is essential to explore its full capabilities and potential applications.

253324-91-3

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253324-91-3 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
1-aMino-3-Methyl-4,5-dihydro-1H-benzo[d]azepin-2(3H)-one is used as a chemical compound in pharmaceutical research and drug development for its potential applications in the treatment of central nervous system disorders or psychiatric conditions. Its unique structure and pharmacological properties make it a promising candidate for the development of new therapeutic agents.
Used in the Treatment of Central Nervous System Disorders:
In the field of neurology, 1-aMino-3-Methyl-4,5-dihydro-1H-benzo[d]azepin-2(3H)-one is used as a potential therapeutic agent for the treatment of central nervous system disorders. Its chemical structure and pharmacological properties suggest that it may have beneficial effects on neurological conditions, although further research is needed to confirm its efficacy and safety.
Used in the Treatment of Psychiatric Conditions:
In the field of psychiatry, 1-aMino-3-Methyl-4,5-dihydro-1H-benzo[d]azepin-2(3H)-one is used as a potential therapeutic agent for the treatment of psychiatric conditions. Its unique chemical structure and pharmacological properties may contribute to the development of new treatments for mental health disorders, pending further research and clinical trials.

Check Digit Verification of cas no

The CAS Registry Mumber 253324-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,3,2 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 253324-91:
(8*2)+(7*5)+(6*3)+(5*3)+(4*2)+(3*4)+(2*9)+(1*1)=123
123 % 10 = 3
So 253324-91-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2O/c1-13-7-6-8-4-2-3-5-9(8)10(12)11(13)14/h2-5,10H,6-7,12H2,1H3

253324-91-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-amino-3-methyl-2,5-dihydro-1H-3-benzazepin-4-one

1.2 Other means of identification

Product number -
Other names (RS)-1-amino-3-methyl-1,3,4,5-tetrahydro-benzo[d]azepin-2-one

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:253324-91-3 SDS

253324-91-3Relevant academic research and scientific papers

METHOD FOR PRODUCING BENZAZEPINONE

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Page/Page column 18, (2008/12/04)

It is an object of the present invention to provide 2-iminocarboxylic acid derivatives, and a practically suitable industrial method for producing benzazepinones in a short process under mild conditions. The present invention provides a method for producing a benzazepinone or a salt thereof, which comprises opening a ring of an isoquinoline derivative and subsequently converting the thus generated amine into a benzazepinone through lactamization reaction.

Classical and dynamic resolution of 1-amino-3-methyl-1,3,4,5- tetrahydrobenzo[d]azepin-2-one

Mitchell, David,Hay, Lynne A.,Koenig, Thomas M.,McDaniel, Stacey,Nissen, Jeffrey S.,Audia, James E.

, p. 3814 - 3819 (2007/10/03)

Two efficient production processes of enantioenriched 1-amino-3-methyl-1,3, 4,5-tetrahydro-benzo[d]azepin-2-one 1 were achieved using the readily available starting materials. A key step in the methodologies is a classical resolution or a dynamic resolution that provides excellent chemical (>80%) yields and enantiomeric excesses (>99.8% ee). The classical resolution was developed on a preparative scale while the dynamic resolution was implemented on a pilot plant scale.

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