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3-(1,3,4-OXADIAZOL-2-YL)ANILINE, with the molecular formula C8H7N3O, is a heterocyclic organic compound characterized by the presence of a 1,3,4-oxadiazole ring and an aniline group. 3-(1,3,4-OXADIAZOL-2-YL)ANILINE is recognized for its diverse applications in research and industry, including the synthesis of pharmaceuticals, agrochemicals, and dyes. Its potential biological and pharmacological activities, such as antiviral and antimicrobial properties, have been a subject of study. Furthermore, the fluorescent properties of 3-(1,3,4-OXADIAZOL-2-YL)ANILINE make it a valuable component in the development of sensors and imaging agents for biological research.

5378-35-8

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5378-35-8 Usage

Uses

Used in Pharmaceutical Synthesis:
3-(1,3,4-OXADIAZOL-2-YL)ANILINE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 3-(1,3,4-OXADIAZOL-2-YL)ANILINE is utilized as a component in the creation of various agrochemicals, enhancing crop protection and management strategies.
Used in Dye Manufacturing:
3-(1,3,4-OXADIAZOL-2-YL)ANILINE is employed as a building block in the manufacturing of dyes, contributing to the colorfastness and performance of these products.
Used in Antiviral and Antimicrobial Research:
3-(1,3,4-OXADIAZOL-2-YL)ANILINE is used as a subject of research for its potential antiviral and antimicrobial properties, with the aim of discovering new treatments and preventive measures against infectious diseases.
Used in Sensor and Imaging Agent Development:
Leveraging its fluorescent properties, 3-(1,3,4-OXADIAZOL-2-YL)ANILINE is used in the development of sensors and imaging agents, which are crucial for enhancing diagnostic capabilities and understanding biological processes in research settings.

Check Digit Verification of cas no

The CAS Registry Mumber 5378-35-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,7 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5378-35:
(6*5)+(5*3)+(4*7)+(3*8)+(2*3)+(1*5)=108
108 % 10 = 8
So 5378-35-8 is a valid CAS Registry Number.

5378-35-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1,3,4-OXADIAZOL-2-YL)ANILINE

1.2 Other means of identification

Product number -
Other names 3-[1,3,4]oxadiazol-2-yl-aniline

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:5378-35-8 SDS

5378-35-8Relevant academic research and scientific papers

THERAPEUTICALLY ACTIVE COMPOUNDS AND THEIR METHODS OF USE

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, (2015/03/31)

Provided are methods of treating a cancer characterized by the presence of a mutant allele of IDH1/2 comprising administering to a subject in need thereof a compound described here.

THERAPEUTICALLY ACTIVE COMPOUNDS AND THEIR METHODS OF USE

-

, (2013/07/31)

Provided are methods of treating a cancer characterized by the presence of a mutant allele of IDH1/2 comprising administering to a subject in need thereof a compound described here.

(N-Isocyanimino)triphenylphosphorane as an Efficient reagent for the synthesis of 1,3,4-Oxadiazoles from 3-substituted benzoic acid derivatives

Ramazani, Ali,Souldozi, Ali

experimental part, p. 3191 - 3198 (2010/08/06)

The reaction of 3-substituted benzoic acid derivatives with (N-isocyanimino) triphenylphosphorane proceeds smoothly at room temperature to afford corresponding 1,3,4-oxadiazoles via an intramolecular aza-Wittig reaction in excellent yields under neutral c

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