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5-Heptyl-[1,3,4]oxadiazol-2-ylamine is a chemical compound characterized by the molecular formula C10H20N4O. It is a member of the oxadiazole group, featuring a seven-carbon heptyl chain attached to a 1,3,4-oxadiazole ring. 5-Heptyl-[1,3,4]oxadiazol-2-ylamine has garnered interest due to its potential applications in various fields, including pharmaceuticals, materials science, and analytical chemistry.

1617-92-1

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1617-92-1 Usage

Uses

Used in Pharmaceutical Applications:
5-Heptyl-[1,3,4]oxadiazol-2-ylamine is used as a potential active pharmaceutical ingredient for its demonstrated antibacterial, antifungal, and antiparasitic properties. Its diverse biological activities make it a candidate for the development of new drugs to combat various infections and diseases.
Used in Materials Science:
In the field of materials science, 5-Heptyl-[1,3,4]oxadiazol-2-ylamine is used as a building block in the synthesis of novel materials. Its unique structure and properties contribute to the creation of innovative compounds with potential applications in various industries.
Used in Analytical Chemistry:
5-Heptyl-[1,3,4]oxadiazol-2-ylamine is used as a fluorescent probe for the detection of metal ions. Its ability to fluoresce in the presence of certain metal ions makes it a valuable tool in analytical chemistry for environmental monitoring and other applications requiring sensitive and selective detection methods.
Used in Environmental Monitoring:
In environmental monitoring, 5-Heptyl-[1,3,4]oxadiazol-2-ylamine is used as a detection agent for monitoring the presence of metal ions in various samples. Its fluorescent properties allow for the sensitive and selective detection of these ions, contributing to the assessment and management of environmental contaminants.
Further research and development of 5-Heptyl-[1,3,4]oxadiazol-2-ylamine will likely uncover additional applications and benefits across different fields, enhancing its utility and potential impact on various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1617-92-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1617-92:
(6*1)+(5*6)+(4*1)+(3*7)+(2*9)+(1*2)=81
81 % 10 = 1
So 1617-92-1 is a valid CAS Registry Number.

1617-92-1SDS

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 5-heptyl-1,3,4-oxadiazol-2-amine

1.2 Other means of identification

Product number -
Other names 5-HEPTYL-[1,3,4]OXADIAZOL-2-YLAMINE

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:1617-92-1 SDS

1617-92-1Relevant academic research and scientific papers

Electrochemical synthesis of 2-amino-5-substituted-1,3,4-oxadiazole derivatives and evaluation of antibacterial activity

Kumar, Sanjeev,Pandey

, p. 252 - 258 (2013/05/09)

Some new 2-amino-5-substituted-1,3,4-oxadiazoles have been synthesized at platinum electrode through the electrochemical oxidation of semicarbazone at room temperature and studied for their antibacterial activity. This is an environmentally benign method in the field of electroorganic synthesis under controlled potential electrolysis in an undivided cell. The electrolysis have been carried out in the acetonitrile solvent and lithium perchlorate is used as a supporting electrolyte. Two platinum plates are used as working as well as counter electrode and saturated calomel electrode as the reference electrode. These compounds have been characterized by microanalyses, IR, Mass, 1H NMR and 13C NMR spectral data. All the compounds have been evaluated for their antibacterial activity against Klebsilla penumoniae, Escherichia coli, Streptococcus aureus and Shigella dysenteriea at 25 and 50 ppm concentrations.

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