CAS 20718-46-1

5-Chloro-4-nitro-2,1,3-benzoselenadiazole

Description:

5-Chloro-4-nitro-2,1,3-benzoselenadiazole is a heterocyclic compound that features a selenadiazole ring fused to a benzene structure, characterized by the presence of chlorine and nitro substituents. This compound typically exhibits a yellow to orange crystalline appearance and is known for its potential applications in organic synthesis and materials science, particularly in the development of electronic materials and dyes. The presence of the chlorine and nitro groups contributes to its reactivity and may influence its electronic properties, making it of interest in various chemical reactions. Additionally, the selenadiazole moiety can impart unique photophysical properties, which are valuable in the design of sensors and optoelectronic devices. As with many heterocyclic compounds, it is essential to handle this substance with care, considering its potential toxicity and environmental impact. Proper safety protocols should be followed when working with this compound in a laboratory setting.

Formula: C₆H₂ClN₃O₂Se

InChI: InChI=1S/C6H2ClN3O2Se/c7-3-1-2-4-5(9-13-8-4)6(3)10(11)12/h1-2H

InChI key: InChIKey=TZPWJERFLDFTSH-UHFFFAOYSA-N

SMILES: N(=O)(=O)C=1C=2C(C=CC1Cl)=N[Se]N2

Synonyms:

• 5-Chloro-4-nitro-2,1,3-benzoselenadiazole
• 2,1,3-Benzoselenadiazole, 5-chloro-4-nitro-
• 5-Chloro-4-nitrobenzo-2,1,3-selenadiazole

2,1,3-Benzoselenadiazole, 5-chloro-4-nitro-

CAS: 20718-46-1

Formula: C₆H₂ClN₃O₂Se

Color and Shape: Solid

Molecular weight: 262.512

Ref: IN-DA002IVO

5-Chloro-4-nitro-2,1,3-benzoselenadiazole

Controlled Product

CAS: 20718-46-1

Applications 5-Chloro-4-nitro-2,1,3-benzoselenadiazole (cas# 20718-46-1) is a compound useful in organic synthesis.
References Turesky, R., et al.: J. Agric. Food Chem., 53, 3248 (2005),

Formula: C₆H₂ClN₃O₂Se

Color and Shape: Neat

Molecular weight: 262.51

Ref: TR-C373890