6-NITRO-3-CARBOXALDEHYDE

6-NITRO-3-CARBOXALDEHYDE - Names and Identifiers

Name	6-Nitro-1H-indazole-3-carboxaldehyde
Synonyms	6-NITRO-3-CARBOXALDEHYDE 6-NITRO INDAZOLE-3-CARBOXALDEHYDE 6-nitro-2H-indazole-3-carbaldehyde 6-NITRO-1H-INDAZOLE-3-CARBALDEHYDE 6-NITRO-1H-INDAZOLE-3-CARBOXALDEHYDE 6-nitro-2H-indazole-3-carboxaldehyde 6-Nitro-1H-indazole-3-carboxaldehyde 6-Nitro-1H-indazole-3-carboxyaldehyde 6-nitro-1H-indazole-3-carboxylic acid 1H-Indazole-3-carboxaldehyde, 6-nitro-
CAS	315203-37-3
InChI	InChI=1/C8H5N3O4/c12-8(13)7-5-2-1-4(11(14)15)3-6(5)9-10-7/h1-3H,(H,9,10)(H,12,13)

6-NITRO-3-CARBOXALDEHYDE - Physico-chemical Properties

Molecular Formula	C8H5N3O3
Molar Mass	191.14
Density	1.733g/cm³
Boling Point	547.1°C at 760 mmHg
Flash Point	284.7°C
Vapor Presure	8.37E-13mmHg at 25°C
Storage Condition	under inert gas (nitrogen or Argon) at 2-8°C
Refractive Index	1.779

6-NITRO-3-CARBOXALDEHYDE - Introduction

It is an organic compound with the chemical formula C8H5N3O3. It is a pale yellow crystalline powder with a strong odor.

Many have a variety of applications. First, it can be used as an important intermediate in organic synthesis. Secondly, it has antibacterial and antiviral activity and may have certain pharmacological effects. In addition, the compound can also be used as a raw material for organic dyes, luminescent agents and explosives.

The preparation of phosphonium can be carried out through the following steps: First, using nitric acid and formaldehyde as raw materials, methyl nitrate is prepared by nitration reaction. The methyl nitrate is then reacted with indazole to form 6-nitro-indazole-3-methanol. Finally, 6-nitro-indazole-3-methanol is oxidized to form a pyridine.

Regarding safety information, it belongs to toxic compounds, which are irritating and corrosive. Appropriate safety measures, such as wearing protective gloves, glasses and protective clothing, should be observed during operation. Avoid contact with skin, eyes and respiratory tract. During use, storage and handling, care should be taken to avoid mixing with combustibles and oxidants to prevent fire or explosion.

Last Update：2024-04-10 22:29:15