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2-(chloromethyl)-5-(2-nitrophenyl)-1,3,4-oxadiazole is a chemical compound belonging to the oxadiazole family, characterized by a molecular formula of C9H6ClN3O3. It features a chloromethyl group and a nitrophenyl group attached to the oxadiazole ring, which endows it with a variety of biological and pharmacological activities. 2-(chloromethyl)-5-(2-nitrophenyl)-1,3,4-oxadiazole has garnered interest in the field of medicinal chemistry for its potential applications in developing new drugs with antibacterial, antifungal, and anticancer properties. Furthermore, it has demonstrated potential as a fluorescent dye and in organic synthesis reactions, making it a significant compound for ongoing research and development.

63002-55-1

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63002-55-1 Usage

Uses

Used in Pharmaceutical Industry:
2-(chloromethyl)-5-(2-nitrophenyl)-1,3,4-oxadiazole is used as a key intermediate in the synthesis of new drugs for its potential antibacterial, antifungal, and anticancer properties. Its unique structural features allow for the development of compounds that can target specific biological pathways, offering novel treatment options for various diseases.
Used in Research and Development:
In the field of medicinal chemistry, 2-(chloromethyl)-5-(2-nitrophenyl)-1,3,4-oxadiazole serves as a valuable compound for research and development. Its diverse range of biological activities and potential applications in drug discovery make it an important subject for further investigation, with the aim of uncovering new therapeutic agents and understanding its mechanisms of action.
Used as a Fluorescent Dye:
2-(chloromethyl)-5-(2-nitrophenyl)-1,3,4-oxadiazole has shown potential as a fluorescent dye due to its unique optical properties. It can be utilized in various applications, such as bioimaging, sensing, and diagnostics, where its fluorescence can provide valuable information about biological processes or the presence of specific molecules.
Used in Organic Synthesis Reactions:
2-(chloromethyl)-5-(2-nitrophenyl)-1,3,4-oxadiazole also finds use in organic synthesis reactions, where its reactive functional groups can be employed to form new chemical entities. Its versatility in synthesis allows for the creation of a wide range of molecules with potential applications in various industries, including pharmaceuticals, materials science, and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 63002-55-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,0 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63002-55:
(7*6)+(6*3)+(5*0)+(4*0)+(3*2)+(2*5)+(1*5)=81
81 % 10 = 1
So 63002-55-1 is a valid CAS Registry Number.

63002-55-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloromethyl-5-(2-nitrophenyl)-1,3,4-oxadiazole

1.2 Other means of identification

Product number -
Other names 1,3,4-OXADIAZOLE, 2-(CHLOROMETHYL)-5-(2-NITROPHENYL)

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:63002-55-1 SDS

63002-55-1Downstream Products

63002-55-1Relevant academic research and scientific papers

Synthesis of 2-chloromethyl-5-aryl-, 2-chloromethyl-5-(5-methyl-2-furyl)-, and 2-chloromethyl-5-(1,5-dimethyl-2-pyrrolyl)-1,3,4-oxadiazoles from tetrazole derivatives

Baranov,Tsypin,Malin,Laskin

, p. 773 - 775 (2007/10/03)

Acetylation of 5-aryltetrazoles, 5-(5-methyl-2-furyl)tetrazole, and 5-(1,5-dimethyl-2-pyrrolyl)tetrazole with chloroacetyl chloride was studied.

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