171006-99-8

Basic information

• Product Name: 1,2,4-Oxadiazol-3-amine,5-propyl-(9CI)
• Synonyms: 1,2,4-Oxadiazol-3-amine,5-propyl-(9CI);5-propyl-1,2,4-oxadiazol-3-amine(SALTDATA: FREE);5-Propyl-1,2,4-oxadiazol-3-amine
• CAS NO: 171006-99-8
• Molecular Formula: C5H9N3O
• Molecular Weight: 127.14446
• Product Categories: AMINEPRIMARY
• Mol File: 171006-99-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2,4-Oxadiazol-3-amine,5-propyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,4-Oxadiazol-3-amine,5-propyl-(9CI)(171006-99-8)
• EPA Substance Registry System: 1,2,4-Oxadiazol-3-amine,5-propyl-(9CI)(171006-99-8)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 171006-99-8(Hazardous Substances Data)

Usage

General Description

1,2,4-Oxadiazol-3-amine,5-propyl-(9CI) is a chemical compound with the molecular formula C5H9N3O. It is a member of the oxadiazole family and contains an amine group and a propyl substituent. 1,2,4-Oxadiazol-3-amine,5-propyl-(9CI) has potential applications in the pharmaceutical industry due to its interesting chemical and biological properties. Its structural features make it suitable for the development of new drugs with diverse therapeutic activities. Furthermore, 1,2,4-Oxadiazol-3-amine,5-propyl-(9CI) can also be used as a building block in organic synthesis for the creation of various functional molecules with specific properties. Overall, this chemical compound has great potential for use in drug discovery and other areas of chemical research.

Upstream product

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Relevant articles and documents

9H-Xanthene-9-carboxylic acid [1,2,4]oxadiazol-3-yl- and (2H-tetrazol-5-yl)-amides as potent, orally available mGlu1 receptor enhancers

Small molecule mGluR1 enhancers based on the lead compound (9H-xanthene-9-carbonyl)-carbamic acid butyl ester derived from random-screening hit diphenylacetyl-carbamic acid ethyl ester were designed and synthesized as useful pharmacological tools for the study of the physiological roles mediated by mGlu1 receptors. The synthesis and the structure-activity relationship of this new class of positive allosteric modulators of mGlu1 receptors will be discussed in detail.

A generalized and efficient synthesis of 3-amino-, 3-(N-alkylamino)-, 3-(N,N-dialkylamino)-5-alkyl-1,2,4-oxadiazoles by irradiation of 3-alkanoylamino-4-phenyl-1,2,5-oxadiazoles (Furazans)

Irradiation of 3-alkanoylamino-4-phenyl-1,2,5-oxadiazoles (furazans) at λ = 310 nm in methanol and in the presence of ammonia, primary or secondary aliphatic amines produced excellent yields of 3-amino-, 3-(N-alkylamino)-, 3-(N,N-dialkylamino)-5-alkyl-1,2