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2-Chloro-6-nitrotoluene
[CAS# 83-42-1]

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Complete supplier list of 2-Chloro-6-nitrotoluene
Identification
Classification Chemical pesticide >> Insecticide intermediate
Name 2-Chloro-6-nitrotoluene
Synonyms 1-Chloro-2-methyl-3-nitrobenzene
Molecular Structure CAS # 83-42-1, 2-Chloro-6-nitrotoluene, 1-Chloro-2-methyl-3-nitrobenzene
Molecular Formula C7H6ClNO2
Molecular Weight 171.58
CAS Registry Number 83-42-1
EC Number 201-475-9
SMILES CC1=C(C=CC=C1Cl)[N+](=O)[O-]
Properties
Melting point 33-37 ºC
Boiling point 238 ºC
Flash point 125 ºC
Water solubility 92 mg/L (20 ºC)
Safety Data
Hazard Symbols symbol symbol symbol   GHS07;GHS08;GHS09 Warning    Details
Hazard Statements H302-H315-H319-H335-H373-H411    Details
Precautionary Statements P260-P264-P264+P265-P270-P273-P280-P301+P317-P302+P352-P305+P351+P338-P319-P321-P330-P332+P317-P337+P317-P362+P364-P391-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H302
Acute toxicityAcute Tox.3H311
Acute toxicityAcute Tox.3H301
Specific target organ toxicity - repeated exposureSTOT RE2H373
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Eye irritationEye Irrit.2H319
Skin irritationSkin Irrit.2H315
Acute toxicityAcute Tox.2H330
Acute toxicityAcute Tox.3H331
Transport Information UN 2433;UN 3457
SDS Available
up Discovory and Applicatios
2-Chloro-6-nitrotoluene is an aromatic compound with the chemical formula C7H6ClNO2. Structurally, it consists of a toluene ring substituted with a chlorine atom at the 2-position and a nitro group at the 6-position. This configuration imparts distinct chemical properties to the molecule, making it a valuable intermediate in various industrial applications. Its discovery and development as a chemical substance were driven by the need to synthesize complex aromatic compounds used in dye, pharmaceutical, and agrochemical industries.

The compound can be synthesized through the nitration of 2-chlorotoluene, a reaction that introduces the nitro group into the aromatic ring. Nitration typically involves the use of concentrated nitric and sulfuric acids under controlled conditions. The resulting product, 2-chloro-6-nitrotoluene, is isolated and purified for further use.

2-Chloro-6-nitrotoluene is primarily used as an intermediate in the synthesis of various chemicals. In the dye industry, it serves as a key precursor for the production of azo dyes and pigments. The nitro and chloro substituents on the aromatic ring make it reactive towards further chemical modifications, such as reduction or substitution reactions, allowing for the creation of a wide range of colorants used in textiles and plastics.

In the pharmaceutical industry, 2-chloro-6-nitrotoluene is employed in the synthesis of active pharmaceutical ingredients (APIs). The presence of both nitro and chloro groups enables selective reactions, making it a useful building block for producing drugs with specific chemical functionalities. Additionally, it can be used in the development of agrochemicals, where its reactive structure allows for the production of herbicides, insecticides, and fungicides.

Despite its usefulness, 2-chloro-6-nitrotoluene must be handled with care, as it is classified as a hazardous material. The compound can be harmful if inhaled, ingested, or if it comes into contact with skin. Prolonged exposure can lead to irritation or more severe health issues, necessitating appropriate safety measures in industrial settings.

Overall, the discovery and application of 2-chloro-6-nitrotoluene have had a significant impact on multiple industries. Its role as a versatile intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals underscores its importance in chemical manufacturing.
Market Analysis Reports
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