CAS 57507-34-3
:3-chloro-4-nitrobenzaldehyde
Description:
3-Chloro-4-nitrobenzaldehyde is an organic compound characterized by its aromatic structure, featuring a benzaldehyde functional group with both a chlorine and a nitro substituent on the aromatic ring. The chlorine atom is located at the meta position (3-position) relative to the aldehyde group, while the nitro group is situated at the para position (4-position). This compound typically appears as a yellow to brown solid and is known for its reactivity due to the presence of both electron-withdrawing groups, which can influence its electrophilic and nucleophilic properties. It is soluble in organic solvents like ethanol and dichloromethane but has limited solubility in water. 3-Chloro-4-nitrobenzaldehyde is often used in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals, as well as in the development of dyes and pigments. Safety precautions should be taken when handling this compound, as it may pose health risks, including irritation to the skin and respiratory system.
Formula:C7H4ClNO3
InChI:InChI=1/C7H4ClNO3/c8-6-3-5(4-10)1-2-7(6)9(11)12/h1-4H
SMILES:c1cc(c(cc1C=O)Cl)N(=O)=O
Synonyms:- 57507-34-3
- Benzaldehyde, 3-Chloro-4-Nitro-
- Wnr Bg Dvh
- 3-Chloro-4-nitrobenzaldehyde
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.
3-Chloro-4-nitrobenzaldehyde
CAS:Formula:C7H4ClNO3Purity:95%Color and Shape:SolidMolecular weight:185.56463-Chloro-4-nitrobenzaldehyde
CAS:<p>3-Chloro-4-nitrobenzaldehyde</p>Purity:98%Molecular weight:185.56g/mol3-Chloro-4-nitrobenzaldehyde
CAS:<p>3-Chloro-4-nitrobenzaldehyde is an aldehyde that is produced by the oxidation of 2-chloro-4-nitrobenzaldehyde. This chemical has been shown to have antitubercular activity in human erythrocytes, and it can be recycled from its reaction product with sodium hypochlorite. 3-Chloro-4-nitrobenzaldehyde has been shown to interact with acidic heterocycles such as oxadiazoles and triazoles. 3-Chloro-4-nitrobenzaldehyde has also been shown to alter the morphology of bacteria, such as subtilis, when exposed to ionic liquids. It is also known to inhibit the growth of Gram positive bacteria and show cytotoxic effects on mammalian cells.</p>Formula:C7H4ClNO3Purity:Min. 95%Molecular weight:185.56 g/mol3-CHLORO-4-NITROBENZALDEHYDE
CAS:Formula:C7H4ClNO3Purity:95%Color and Shape:Light yellow powderMolecular weight:185.563-Chloro-4-nitrobenzaldehyde
CAS:Controlled ProductFormula:C7H4ClNO3Color and Shape:NeatMolecular weight:185.565




