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3663-39-6

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3663-39-6 Usage

Description

3-METHYL-1,2,4-OXADIAZOL-5-AMINE is a heterocyclic chemical compound characterized by the molecular formula C3H5N3O. It features an oxadiazole ring fused with an amine group, which endows it with unique structural and functional properties. 3-METHYL-1,2,4-OXADIAZOL-5-AMINE is recognized for its role as a versatile building block in the synthesis of a wide array of pharmaceuticals, agrochemicals, and other organic compounds. Its distinctive attributes make it a valuable component in various chemical and biological applications, and it also holds promise as a drug candidate due to its demonstrated biological activity and pharmacological properties. However, due to potential health risks, careful handling and proper safety measures are essential when working with this compound.

Uses

Used in Pharmaceutical Industry:
3-METHYL-1,2,4-OXADIAZOL-5-AMINE is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its incorporation into drug molecules can enhance their therapeutic efficacy and pharmacological properties, making it an indispensable component in the development of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-METHYL-1,2,4-OXADIAZOL-5-AMINE serves as a crucial building block for the creation of novel agrochemicals. Its unique structure contributes to the development of more effective and targeted pesticides, herbicides, and other agricultural chemicals, thereby improving crop protection and yield.
Used in Organic Synthesis:
3-METHYL-1,2,4-OXADIAZOL-5-AMINE is employed as a versatile reagent in organic synthesis. Its ability to form stable and functionalized products makes it a preferred choice for the synthesis of complex organic compounds, including those with potential applications in materials science, dyes, and other specialty chemicals.
Used in Drug Discovery:
3-METHYL-1,2,4-OXADIAZOL-5-AMINE is recognized for its potential as a drug candidate. Its biological activity and pharmacological properties are being explored for the development of new therapeutic agents, particularly in the areas of oncology, cardiovascular diseases, and neurological disorders. Its unique structure allows for the design of molecules with specific targeting and action mechanisms, offering new avenues for treatment and intervention.

Check Digit Verification of cas no

The CAS Registry Mumber 3663-39-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,6 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3663-39:
(6*3)+(5*6)+(4*6)+(3*3)+(2*3)+(1*9)=96
96 % 10 = 6
So 3663-39-6 is a valid CAS Registry Number.

3663-39-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methyl-1,2,4-oxadiazol-5-amine

1.2 Other means of identification

Product number -
Other names 3-METHYL-1,2,4-OXADIAZOL-5-AMINE

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:3663-39-6 SDS

3663-39-6Relevant articles and documents

ANTIBIOTIC COMPOUNDS

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Page/Page column 75; 76, (2018/03/25)

The present invention relates to antibiotic compounds of formula (I), to compositions containing these compounds and to methods of treating bacterial diseases and infections using the compounds. The compounds find application in the treatment of infection with, and diseases caused by, Gram-positive and/or Gram-negative bacteria, and in particular in the treatment of infection with, and diseases caused by, Neisseria gonorrhoeae.

15N NMR SPECTROSCOPY - APPLICATION IN HETEROCYCLIC CHEMISTRY

Fritz, H.

, p. 559 - 570 (2007/10/02)

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