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5-ISOPROPYL-1,3,4-OXADIAZOL-2-AMINE, also known as 2-Amino-5-isopropyl-1,3,4-oxadiazole, is a chemical compound with the molecular formula C5H10N4O. It is a derivative of oxadiazole and contains an isopropyl group. 5-ISOPROPYL-1,3,4-OXADIAZOL-2-AMINE is characterized by its unique chemical structure and properties, making it a versatile and valuable compound in the field of organic chemistry.

65283-97-8

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65283-97-8 Usage

Uses

Used in Pharmaceutical Industry:
5-ISOPROPYL-1,3,4-OXADIAZOL-2-AMINE is used as an intermediate in the synthesis of various pharmaceuticals for its ability to enhance the biological activity of the final drug products. Its unique structure allows for the development of new therapeutic agents with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, 5-ISOPROPYL-1,3,4-OXADIAZOL-2-AMINE is used as a building block in the production of agrochemicals, such as pesticides and herbicides. Its incorporation into these products can lead to enhanced performance and selectivity, contributing to more effective and targeted pest control.
Used in Organic Synthesis:
5-ISOPROPYL-1,3,4-OXADIAZOL-2-AMINE serves as a valuable building block in organic synthesis, allowing for the creation of a wide range of chemical compounds with diverse applications. Its unique structure and reactivity make it a useful component in the synthesis of various organic molecules.
Used as a Reagent in Chemical Research:
In the field of chemical research, 5-ISOPROPYL-1,3,4-OXADIAZOL-2-AMINE is utilized as a reagent to facilitate various chemical reactions and processes. Its unique properties enable researchers to explore new reaction pathways and develop innovative synthetic methods, further expanding the scope of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 65283-97-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,2,8 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65283-97:
(7*6)+(6*5)+(5*2)+(4*8)+(3*3)+(2*9)+(1*7)=148
148 % 10 = 8
So 65283-97-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H9N3O/c1-3(2)4-7-8-5(6)9-4/h3H,1-2H3,(H2,6,8)

65283-97-8 Well-known Company Product Price

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  • Aldrich

  • (CBR01453)  5-Isopropyl-1,3,4-oxadiazol-2-amine  AldrichCPR

  • 65283-97-8

  • CBR01453-1G

  • 2,901.60CNY

  • Detail

65283-97-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-propan-2-yl-1,3,4-oxadiazol-2-amine

1.2 Other means of identification

Product number -
Other names 5-Isopropyl-[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:65283-97-8 SDS

65283-97-8Relevant academic research and scientific papers

ANTIBIOTIC COMPOUNDS

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Page/Page column 110; 111, (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.

Synthesis of 2-amino-1,3,4-oxadiazoles and 2-Amino-1,3,4-thiadiazoles via sequential condensation and I2-mediated oxidative C-O/C-S bond formation

Niu, Pengfei,Kang, Jinfeng,Tian, Xianhai,Song, Lina,Liu, Hongxu,Wu, Jie,Yu, Wenquan,Chang, Junbiao

, p. 1018 - 1024 (2015/01/30)

2-Amino-substituted 1,3,4-oxadiazoles and 1,3,4-thiadiazoles were synthesized via condensation of semicarbazide/thiosemicarbazide and the corresponding aldehydes followed by I2-mediated oxidative C-O/C-S bond formation. This transition-metal-free sequential synthesis process is compatible with aromatic, aliphatic, and cinnamic aldehydes, providing facile access to a variety of diazole derivatives bearing a 2-amino substituent in an efficient and scalable fashion.

INHIBITION OF P38 KINASE ACTIVITY USING SUBSTITUTED HETEROCYCLIC UREAS

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Page/Page column 16, (2012/03/10)

This invention relates to the use of a group of aryl ureas in treating cytokine mediated diseases, other than cancer and proteolytic enzyme mediated diseases, other than cancer, and pharmaceutical compositions for use in such therapy.

INHIBITION OF RAF KINASE USING SUBSTITUTED HETEROCYCLIC UREAS

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Page/Page column 16, (2010/11/28)

Methods of treating tumors mediated by raf kinase, with substituted urea compounds, and such compounds per se.

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