1-chloro-3-methyl-5-nitro-benzene
1-chloro-3-methyl-5-nitro-benzene
CAS: 16582-38-0
Molecular Formula: C7H6ClNO2
1-chloro-3-methyl-5-nitro-benzene - Names and Identifiers
| Name | 1-chloro-3-methyl-5-nitro-benzene |
| Synonyms | NSC 169207 3-Chlor-5-nitrotoluene 3-CHLORO-5-NITROTOLUENE 5-Chloro-3-nitrotoluene 1-chloro-3-methyl-5-nitro-benzene Benzene, 1-chloro-3-methyl-5-nitro- |
| CAS | 16582-38-0 |
| InChI | InChI=1/C7H6ClNO2/c1-5-2-6(8)4-7(3-5)9(10)11/h2-4H,1H3 |
1-chloro-3-methyl-5-nitro-benzene - Physico-chemical Properties
| Molecular Formula | C7H6ClNO2 |
| Molar Mass | 171.58 |
| Density | 1.324 |
| Melting Point | 54-55℃ |
| Boling Point | 253℃ |
| Flash Point | 107℃ |
| Vapor Presure | 0.0288mmHg at 25°C |
| Appearance | Solid |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1. |
1-chloro-3-methyl-5-nitro-benzene - Introduction
The chemical formula is C7H6ClNO2, often referred to as 3-chloro-5-nitrotoluene (3-chloro-5-nitrotoluene).
Nature:
is a colorless to pale yellow crystalline solid with a pungent odor. It is almost insoluble in water at room temperature, but can be dissolved in organic solvents, such as ethanol and dichloromethane.
Use:
is an important organic synthesis intermediates. It is mainly used in the synthesis of other organic compounds, in particular the preparation of glyphosate. Glyphosate is an active ingredient widely used in herbicides to control various weeds.
Method:
The main synthetic route of the toluene is through the chlorination and nitration reaction. First, toluene is reacted with chlorine gas under appropriate reaction conditions to produce 1-chloro-3-methylbenzene. Then, 1-chloro-3-methylbenzene was reacted with concentrated nitric acid to produce a quartz ring.
Safety Information:
is a toxic compound that should be handled and stored under appropriate laboratory conditions. It may cause irritation and damage to the human skin, eyes and respiratory tract, so appropriate personal protective equipment such as protective gloves, goggles and gas masks must be worn during operation. In addition, care should be taken to avoid contact with fire sources to prevent fire or explosion.
Please note that the use, preparation and handling of chemicals should be carried out under the guidance of professionals and in accordance with the appropriate safety procedures.
Nature:
is a colorless to pale yellow crystalline solid with a pungent odor. It is almost insoluble in water at room temperature, but can be dissolved in organic solvents, such as ethanol and dichloromethane.
Use:
is an important organic synthesis intermediates. It is mainly used in the synthesis of other organic compounds, in particular the preparation of glyphosate. Glyphosate is an active ingredient widely used in herbicides to control various weeds.
Method:
The main synthetic route of the toluene is through the chlorination and nitration reaction. First, toluene is reacted with chlorine gas under appropriate reaction conditions to produce 1-chloro-3-methylbenzene. Then, 1-chloro-3-methylbenzene was reacted with concentrated nitric acid to produce a quartz ring.
Safety Information:
is a toxic compound that should be handled and stored under appropriate laboratory conditions. It may cause irritation and damage to the human skin, eyes and respiratory tract, so appropriate personal protective equipment such as protective gloves, goggles and gas masks must be worn during operation. In addition, care should be taken to avoid contact with fire sources to prevent fire or explosion.
Please note that the use, preparation and handling of chemicals should be carried out under the guidance of professionals and in accordance with the appropriate safety procedures.
Last Update：2024-04-10 22:29:15
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View History
1-chloro-3-methyl-5-nitro-benzene
3-methyl-2-butenoicacimethylester
BOC-3-IODO-L-ALANINE METHYL ESTER
(hydroxymethyl)-phosphonicacidiethylester
3-methyl-2-butenoicacimethylester
BOC-3-IODO-L-ALANINE METHYL ESTER
(hydroxymethyl)-phosphonicacidiethylester