6061-04-7

Basic information

• Product Name: Ethene, 1,1-dichloro-2-nitro-
• CAS NO: 6061-04-7
• Molecular Formula: C2HCl2NO2
• Molecular Weight: 141.941
• Mol File: 6061-04-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Ethene, 1,1-dichloro-2-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethene, 1,1-dichloro-2-nitro-(6061-04-7)
• EPA Substance Registry System: Ethene, 1,1-dichloro-2-nitro-(6061-04-7)

Safety Data

• Hazardous Substances Data: 6061-04-7(Hazardous Substances Data)

Usage

General Description

Ethene, 1,1-dichloro-2-nitro- is a chemical compound with the molecular formula C2H2Cl2NO2. It is a colorless liquid at room temperature and is classified as a chlorinated nitroalkene. Ethene, 1,1-dichloro-2-nitro- is commonly used in the synthesis of complex organic molecules and is also known for its use in the production of pesticides and herbicides. It is considered to be a potential environmental and human health hazard due to its toxic and carcinogenic properties. Additionally, exposure to ethene, 1,1-dichloro-2-nitro- can cause irritation to the skin, eyes, and respiratory system. As a result, proper safety precautions and handling procedures should be followed when working with this chemical.

Upstream product

• 75-35-4 1,1-Dichloroethylene 
• 7705-08-0 iron(III) chloride 
• 64326-81-4 1,1,1-trichloro-2-nitroethane 

Downstream Products

• 69425-68-9 N,N'-dimethyl-2-nitro-N,N'-diphenylethene-1,1-diamine 
• 19419-96-6 1,1-di(ethylsulfanyl)-2-nitroethylene 
• 79506-31-3 1,1-di(p-tolyloxy)-2-nitroethene 
• 79506-30-2 1,1-diphenoxy-2-nitroethene 
• 150824-47-8 1-[N-(2-chloro-5-pyridylmethyl)-N-n-ethylamino]-1-methylamino-2-nitroethylene 
• 101336-63-4 imidacloprid 
• 150824-47-8 nitenpiram 
• 1445-69-8 2,3-dihydrophthalazine-1,4-dione 

Relevant articles and documents

1. 1 - Dichloro - 2 - nitro-ethylene and synthesis method of nitenpyram (by machine translation)

The present invention provides a 1, 1 - dichloro - 2 - nitro-ethylene and nitenpyram synthetic method. 1. 1 - Dichloro - 2 - nitroethylene synthesis method, comprises the following steps: the 1, 1, 1 - trichloro - 2 - nitro-ethane with caustic soda in a microchannel reactor reaction, the obtained product delaminated, congeals the feed liquid, is 1, 1 - dichloro - 2 - [...]. The invention in the micro-channel is performed in a reactor, which has a large specific surface area, can improve the 1, 1, 1 - trichloro - 2 - nitro-ethane with caustic soda contact efficiency, thus improving the response of the raw materials, to improve the product yield. By using micro-channel reactor, 1, 1 - dichloro - 2 - nitroethylene yield as high as 90% or more, and also to increase the purity of 90% or more. This from the side also illustrate the invention to improve the utilization rate of caustic soda, alkali caused by pollution, salt pollution the intensity is reduced, to reduce the difficulty of tail water treatment. (by machine translation)

METHOD FOR SEPARATING AND PURIFYING alpha- UNSATURATED AMINE COMPOUND

A method for purifying an α-unsaturated amine compound represented by Formula (1), the method comprising a step of extracting with water the compound of Formula (1) from a crude product of the α-unsaturated amine compound represented by Formula (1), and a step of extracting with a pyridine solvent the α-unsaturated amine compound of Formula (1) from the aqueous solution containing the compound of Formula (1) obtained in the previous step to obtain a pyridine solvent solution of the compound of Formula (1): wherein R1 represents a hydrogen atom, a C1-4 alkyl group, a halo C1-4 alkyl group, a C1-4 alkoxy-C1-4 alkyl group, a C7-9 aralkyl group, or an optionally substituted phenyl group, R2 represents a hydrogen atom, a C1-4 alkyl group, or a C7-9 aralkyl group, and R3 represents a hydrogen atom, a C1-5 alkyl group, a halo C1-4 alkyl group, a hydroxy C1-4 alkyl group, a C1-4 alkoxy-C1-4 alkyl group, C2-4 alkenyl group, or a C7-9 aralkyl group.

1,1,1-trichloro-2-nitroethane production

Methods for the production of 1,1,1-trihalogeno-2-nitroethanes from 1,1-dihalogenoethylene by using nitric acid or its salt and hydrogen chloride or hydrogen bromide or its salt, and for the production of α-unsaturated amines from the 1,1,1-trihalogeno-2-nitroethanes which are useful as insecticides.