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[1,2,5]Oxadiazolo[3,4-b]pyrazine,4,5,6,7-tetrahydro-4,7-dimethyl-,1-oxide(9CI) is a bicyclic heterocyclic compound with the molecular formula C8H10N4O2. It is an oxide derivative of 4,5,6,7-tetrahydro-4,7-dimethyl-[1,2,5]oxadiazolo[3,4-b]pyrazine. This chemical compound possesses unique structural properties and potential biological activities, making it a promising candidate for applications in the field of medicinal chemistry and pharmaceuticals.

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  • 98778-10-0 Structure
  • Basic information

    1. Product Name: [1,2,5]Oxadiazolo[3,4-b]pyrazine,4,5,6,7-tetrahydro-4,7-dimethyl-,1-oxide(9CI)
    2. Synonyms: [1,2,5]Oxadiazolo[3,4-b]pyrazine,4,5,6,7-tetrahydro-4,7-dimethyl-,1-oxide(9CI);4,7-DIMETHYL-4,5,6,7-TETRAHYDRO[1,2,5]OXADIAZOLO[3,4-B]PYRAZINE 1-OXIDE
    3. CAS NO:98778-10-0
    4. Molecular Formula: C6 H10 N4 O2
    5. Molecular Weight: 170.17
    6. EINECS: N/A
    7. Product Categories: PIPERIDINE
    8. Mol File: 98778-10-0.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: [1,2,5]Oxadiazolo[3,4-b]pyrazine,4,5,6,7-tetrahydro-4,7-dimethyl-,1-oxide(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: [1,2,5]Oxadiazolo[3,4-b]pyrazine,4,5,6,7-tetrahydro-4,7-dimethyl-,1-oxide(9CI)(98778-10-0)
    11. EPA Substance Registry System: [1,2,5]Oxadiazolo[3,4-b]pyrazine,4,5,6,7-tetrahydro-4,7-dimethyl-,1-oxide(9CI)(98778-10-0)
  • 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: 98778-10-0(Hazardous Substances Data)

98778-10-0 Usage

Uses

Used in Medicinal Chemistry:
[1,2,5]Oxadiazolo[3,4-b]pyrazine,4,5,6,7-tetrahydro-4,7-dimethyl-,1-oxide(9CI) is used as a building block for the synthesis of other compounds with similar or improved pharmacological properties. Its unique structure and potential biological activities contribute to the development of new drugs and therapeutic agents.
Used in Pharmaceutical Research:
In the pharmaceutical industry, [1,2,5]Oxadiazolo[3,4-b]pyrazine,4,5,6,7-tetrahydro-4,7-dimethyl-,1-oxide(9CI) is used for further research and investigation into its potential biological activities and toxicological profiles. Understanding these aspects can help in the development of safer and more effective drugs based on this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 98778-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,7,7 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 98778-10:
(7*9)+(6*8)+(5*7)+(4*7)+(3*8)+(2*1)+(1*0)=200
200 % 10 = 0
So 98778-10-0 is a valid CAS Registry Number.

98778-10-0SDS

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 4,7-dimethyl-3-oxido-5,6-dihydro-[1,2,5]oxadiazolo[3,4-b]pyrazin-3-ium

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:98778-10-0 SDS

98778-10-0Relevant articles and documents

Synthesis and Chemistry of Some Furazano- and Furoxanopiperazines

Willer, Rodney L.,Moore, Donald W.

, p. 5123 - 5127 (2007/10/02)

A series of N,N'-disubstituted furazano- and furoxanopiperazines 1a-d and 2b-d have been synthesized from N,N'-disubstituted 2,3-piperazinedione dioximes 5a-d by base-promoted dehydration and by basic potassium ferricyanide oxidation, respectively.The N,N'-disubstituted 2,3-piperazinedione dioximes were synthesized by reacting the appropriate N,N'-disubstituted ethylenediamine with dichloroglyoxime.Also studied was the reaction of 3,4-diaminofurazan with glyoxal and formaldehyde.The compounds have been studied by 1H and 13C NMR spectroscopy.

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