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Octahydropyrazino[2,1-c][1,4]oxazine dihydrochloride is a heterocyclic chemical compound that serves as a dihydrochloride salt with potential anxiolytic and sedative properties. It is utilized in pharmaceutical research and drug development, primarily due to its capacity to act as a positive allosteric modulator of the GABAA receptor. This action enhances the inhibitory effects of the neurotransmitter GABA, which may underlie its anxiolytic and sedative effects. Ongoing research is focused on exploring its therapeutic applications and understanding its pharmacological mechanisms of action, particularly in the treatment of anxiety and other central nervous system disorders.

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  • 1257998-65-4 Structure
  • Basic information

    1. Product Name: Octahydropyrazino[2,1-c][1,4]oxazine dihydrochloride
    2. Synonyms: Octahydropyrazino[2,1-C][1,4]Oxazine Hydrochloride;Octahydropyrazino[2,1-C][1,4]Oxazine Hydrochloride(WX110611S1);OCTAHYDROPYRAZINO[2,1-C][1,4]OXAZINE 2HCL
    3. CAS NO:1257998-65-4
    4. Molecular Formula: C7H16Cl2N2O
    5. Molecular Weight: 215.12074
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1257998-65-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Octahydropyrazino[2,1-c][1,4]oxazine dihydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: Octahydropyrazino[2,1-c][1,4]oxazine dihydrochloride(1257998-65-4)
    11. EPA Substance Registry System: Octahydropyrazino[2,1-c][1,4]oxazine dihydrochloride(1257998-65-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1257998-65-4(Hazardous Substances Data)

1257998-65-4 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
Octahydropyrazino[2,1-c][1,4]oxazine dihydrochloride is used as a research compound for its potential anxiolytic and sedative properties. It is valued for its ability to modulate the GABAA receptor, which is crucial for the treatment of anxiety and other central nervous system disorders.
Used in the Treatment of Anxiety:
In the field of mental health, Octahydropyrazino[2,1-c][1,4]oxazine dihydrochloride is used as a potential therapeutic agent for anxiety disorders. Its mechanism of action involves enhancing the inhibitory neurotransmission mediated by GABA, which can help in reducing anxiety symptoms.
Used in the Development of Central Nervous System Therapies:
Octahydropyrazino[2,1-c][1,4]oxazine dihydrochloride is utilized in the development of treatments for various central nervous system disorders. Its role as a positive allosteric modulator of the GABAA receptor positions it as a candidate for the management of conditions that involve dysregulation of the GABAergic system.

Check Digit Verification of cas no

The CAS Registry Mumber 1257998-65-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,7,9,9 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1257998-65:
(9*1)+(8*2)+(7*5)+(6*7)+(5*9)+(4*9)+(3*8)+(2*6)+(1*5)=224
224 % 10 = 4
So 1257998-65-4 is a valid CAS Registry Number.

1257998-65-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name octahydropyrazino[2,1-c][1,4]oxazine hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:1257998-65-4 SDS

1257998-65-4Relevant articles and documents

PEPTIDE DEFORMYLASE INHIBITORS

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Page/Page column 83, (2013/06/27)

The present invention relates to {2-(alkyl)-3-[2-(5-fluoro-4-pyrimidinyl)hydrazino]-3- oxopropyl}hydroxyformamide compounds of Formula (I): or pharmaceutically acceptable salts thereof, corresponding pharmaceutical compositions, processes for making and use of such compounds in the inhibition of bacterial peptide deformylase (PDF) activity and in treatment methods for bacterial infections

THIAZOLE SULFONAMIDE AND OXAZOLE SULFONAMIDE KINASE INHIBITORS

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Page/Page column 134-135, (2010/10/03)

The present invention provides thiazole sulfonamide and oxazole sulfonamide compounds, compositions containing the same, as well as processes for the preparation and methods for their use as pharmaceutical agents

THIAZOLE AND OXAZOLE KINASE INHIBITORS

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Page/Page column 209, (2009/04/25)

The present invention provides thiazole and oxazole compounds, compositions containing the same, as well as processes for the preparation and methods for their use as pharmaceutical agents.

PEPTIDE DEFORMYLASE INHIBITORS

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Page/Page column 88, (2009/06/27)

The present invention is directed to certain {2-(alkyl)-3-[2-(5-fluoro-4-pyrimidinyl)hydrazino]-3-oxopropyl}hydroxyformamide derivatives, compositions containing them, the use of such compounds in the inhibition of bacterial peptide deformylase (PDF) activity, and in the treatment of bacterial infections. Specifically, the invention is directed to compounds of formula (I), wherein R1, R2 and R3 are defined herein and to pharmaceutically acceptable salts thereof. The compounds of this invention are bacterial peptide deformylase inhibitors and can be useful in the treatment of bacterial infections.

Imidazopyridine Kinase Inhibitors

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Page/Page column 95, (2009/01/20)

The present invention provides imidazopyridine compounds, compositions containing the same, as well as processes for the preparation and methods for their use as pharmaceutical agents.

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