2-Chloro-6-nitrobenzaldehyde

Basic Information

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CAS Number

6361-22-4

Molecular Formula

C7H4ClNO3

Molecular Weight

185.56 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Carboxylic Acids

Basic Chemical Raw Materials Organic Chemicals Aldehydes

Fine Chemicals Dyes and Pigments Organic Dyes

Agricultural Chemicals Pesticides Herbicides

Basic Physical Properties

Melting Point

68.0 to 72.0 deg-C

Boiling Point

298.8°C at 760 mmHg

Density

1.485

Flash Point

134.5°C

Refractive Index

1.63

SMILES

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[O-][N+](=O)c1cccc(Cl)c1C=O

InChI

InChI=1S/C7H4ClNO3/c8-6-2-1-3-7(9(11)12)5(6)4-10/h1-4H

InChIKey

RZDOUWDCYULHJX-UHFFFAOYSA-N

LogP

2.58390

Complexity

192

Safety Information

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Hazard Statement

H315 Causes skin irritation
Skin corrosion/irritation

H319 Causes serious eye irritation
Serious eye damage/eye irritation

Synonyms & References

English

2-Chloro-6-nitrobenzaldehyde
2-NITRO-6-CHLOROBENZALDEHYDE
Benzaldehyde,2-chloro-6-nitro-
Benzaldehyde, 2-chloro-6-nitro-
RZDOUWDCYULHJX-UHFFFAOYSA-N
PubChem17009
KSC497Q1L
2-chloro-6-nitro-benzaldehye
2-chloro-6-nitro-benzaldehyde
RZDOUWDCYULHJX-UHFFFAOYSA-
BBL100330
2-chloro-6-nitrobenzaldehyde

MDL Number

MFCD00007204

Customs Code

2913000090

FAQ

What are the physical and chemical properties of 2-Chloro-6-nitrobenzaldehyde (CAS: 6361-22-4)?

2-Chloro-6-nitrobenzaldehyde is a crystalline solid with a molecular weight of approximately 228.04 g/mol. Its solubility in water is low, with a solubility of about 0.1 g/L at 25°C. Reactivity is moderate, showing typical reactivity of benzaldehydes, including electrophilic aromatic substitution and nucleophilic addition reactions. It is highly reactive towards reducing agents and can undergo hydrolysis under basic conditions.

How is 2-Chloro-6-nitrobenzaldehyde (CAS: 6361-22-4) typically synthesized?

2-Chloro-6-nitrobenzaldehyde is commonly synthesized via nitration of 2-chlorobenzaldehyde followed by reduction of the nitro group. Alternatively, it can be prepared by chlorination of 6-nitrobenzaldehyde. The synthesis typically involves the use of concentrated nitric and sulfuric acids as reagents, with careful temperature control to ensure selectivity and yield.

What industries use 2-Chloro-6-nitrobenzaldehyde (CAS: 6361-22-4)?

2-Chloro-6-nitrobenzaldehyde finds applications in pharmaceuticals, where it serves as a precursor for the synthesis of various organic compounds and drugs. It is also used in the production of dyes and pigments, as well as in the development of sensors and semiconductors. The compound's unique chemical properties make it valuable in these industries for its reactivity and potential in organic synthesis.

What precautions should be taken when handling 2-Chloro-6-nitrobenzaldehyde (CAS: 6361-22-4)?

When handling 2-Chloro-6-nitrobenzaldehyde, proper personal protective equipment (PPE) such as gloves, goggles, and a lab coat should be worn. Work should be conducted in a well-ventilated area or a fume hood to minimize inhalation risks. Spills should be cleaned up immediately using appropriate safety protocols. Always refer to the Material Safety Data Sheet (MSDS/SDS) for detailed safety information and emergency procedures.