2567-14-8

Basic information

• Product Name: 1,1,3-TRICHLOROPROPENE
• Synonyms: 1,1,3-trichloro-1-propen;1,1,3-Trichloro-1-propene;1,3,3-Trichloro-2-propene;3,3-Dichloroallyl chloride;3,3-dichloroallylchloride;Propene, 1,1,3-trichloro-;1,1,3-TRICHLOROPROPENE;BRN 1738076
• CAS NO: 2567-14-8
• Molecular Formula: C₃H₃Cl₃
• Molecular Weight: 145.41
• EINECS: 219-903-8
• Mol File: 2567-14-8.mol
• Article Data: 31

Chemical Properties

• Melting Point: -30°C (estimate)
• Boiling Point: 131.55°C
• Flash Point: 48.9°C
• Appearance: /
• Density: 1.3670 (estimate)
• Vapor Pressure: 11.3mmHg at 25°C
• Refractive Index: 1.4895 (estimate)
• CAS DataBase Reference: 1,1,3-TRICHLOROPROPENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,3-TRICHLOROPROPENE(2567-14-8)
• EPA Substance Registry System: 1,1,3-TRICHLOROPROPENE(2567-14-8)

Safety Data

• RIDADR: 1993
• HazardClass: 3.2
• PackingGroup: III
• Hazardous Substances Data: 2567-14-8(Hazardous Substances Data)

Usage

General Description

1,1,3-Trichloropropene is a colorless liquid chemical compound with the formula C3H3Cl3. It is primarily used as a solvent and as an intermediate in the synthesis of other chemicals. It is also used as a pesticide and soil fumigant. It has a sharp, pungent odor and is highly flammable. Exposure to 1,1,3-Trichloropropene can cause respiratory irritation, skin irritation, and central nervous system depression. It is considered to be a hazardous chemical and proper safety precautions should be taken when handling and storing it. Additionally, 1,1,3-Trichloropropene is harmful if swallowed or absorbed through the skin, and can cause long-term health effects if not properly managed.

InChI:InChI=1/C3H3Cl3/c4-2-1-3(5)6/h1H,2H2

Upstream product

• 187737-37-7 propene 
• 18495-30-2 1,1,2,3-tetrachloropropane 
• 98142-55-3 bis(1-trichloromethyl-2-chloroethyl)disulfide 
• 1070-78-6 1,1,1,3-tetrachloropropane 
• 74-87-3 methylene chloride 
• 79-01-6 Trichloroethylene 
• 142-28-9 1,3-Dichloropropane 
• 627-30-5 1-chloro-3-hydroxypropane 
• 110-80-5 2-ethoxy-ethanol 
• 13749-37-6 3-bromo-1,1,1-trichloropropane 
• 7732-18-5 water 
• 2233-00-3 3,3,3-trichloro-1-propene 
• 7664-93-9 sulfuric acid 
• 64-19-7 acetic acid 

Downstream Products

• 100124-05-8 1,4-bis-(3,3-dichloro-allyl)-benzene 
• 98588-96-6 (4-chloro-phenyl)-(3,3-dichloro-allyl)-ether 
• 100517-46-2 3,5-dinitro-benzoic acid-(3,3-dichloro-allyl ester) 
• 565-64-0 2,3-dichloropropanoic acid 
• 563-58-6 1,1-dichloropropene 
• 3039-55-2 3,3-dichloro-2-propen-1-ol 
• 98199-04-3 bis-(3,3-dichloro-allyl)-amine 
• 38862-78-1 1,1-dichloro-3-phenylpropene 
• 54378-60-8 N-(2-Bromo-2,2-dichloro-1-chloromethyl-ethyl)-benzenesulfonamide 
• 54378-59-5 C₉H₈Br₂Cl₃NO₂S 
• 61007-62-3 1,1,3-Trichlor-2-p-xylylpropan 
• 1576-26-7 N'-Methoxy-N'-<3.3-dichlor-allyl>-N-<4-chlor-phenyl>-harnstoff 
• 38491-37-1 3.3-Dichlorprop-2-enyl-phenylsulfid 
• 64843-40-9 4-nitro-benzoic acid-(3,3-dichloro-allyl ester) 

Relevant articles and documents

MOLYBDENUM HEXACARBONYL - A CATALYST FOR THE DEHYDROCHLORINATION OF COMPOUNDS CONTAINING A TRICHLOROMETHYL GROUP

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PREPARATION OF 2,3,3,3-TETRAFLUOROPROPENE AND INTERMEDIATES THEREOF

The present invention provides a process for preparation of 2,3,3,3-tetrafluoropropene and intermediates thereof. Owing to its low global warming potential and zero ozone depleting potential, it is been proposed as a replacement for existing chlorofluorocarbons and hydrofluorocarbons as refrigerant.

Method for eliminating hydrogen chloride by catalytic cracking of chloralkane

The invention discloses a method for eliminating hydrogen chloride by catalytic cracking of chloralkane, comprising the following steps of: carrying out a cracking reaction on chloralkane under the action of a biomass-based nitrogen-doped carbon catalyst to eliminate hydrogen chloride so as to prepare corresponding olefin, wherein the biomass-based nitrogen-doped carbon catalyst is prepared by carbonizing biomass or a mixture of biomass and a nitrogen source at 400-1000 DEG C, and the biomass is selected from at least one of bamboo processing leftovers, wood processing leftovers, plant straws,plant leaves, cereals, beans, cereal processing leftovers, bean processing leftovers and livestock manure. The method disclosed by the invention has the advantages of simple preparation process, easily available raw materials, low cost, strong process controllability, easiness in large-scale production, high catalytic cracking conversion rate of the chloralkane, high product selectivity, low energy consumption and the like.