Conditions | Yield |
---|---|
With methyl diethylphosphinate at 180℃; for 14.5h; | 56% |
With potassium hydroxide | |
at 250 - 420℃; |
trichloro(heptachloropropyl)silane
perchloropropene
Conditions | Yield |
---|---|
With aluminium trichloride at 160 - 180℃; | 52% |
pentachloro-2-(trimethylsiloxy)propene
A
chloro-trimethyl-silane
B
pentachloroacetone
C
perchloropropene
Conditions | Yield |
---|---|
With phosphorus pentachloride at 150℃; for 15h; Yields of byproduct given; | A 52% B n/a C n/a |
With phosphorus pentachloride at 150℃; for 15h; Yield given. Title compound not separated from byproducts; | A 52% B n/a C n/a |
Conditions | Yield |
---|---|
With hydrogen |
Conditions | Yield |
---|---|
at 350℃; |
Conditions | Yield |
---|---|
With aluminium trichloride |
heptachloro-butyraldehyde
perchloropropene
Conditions | Yield |
---|---|
With sodium ethanolate |
Conditions | Yield |
---|---|
With chlorine at 200℃; Irradiation; |
Conditions | Yield |
---|---|
With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride In chloroform |
perchloroallene
perchloropropene
Conditions | Yield |
---|---|
With chlorine In dichloromethane |
heptachlorobutyryl chloride
perchloropropene
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide |
propene
A
1,1,1,3,3-pentachloropropene
B
1,1-dichloropropene
C
3,3-dichloroallyl chloride
D
perchloropropene
E
1,1,3,3-tetrachloro-1-propene
F
propenyl chloride
Conditions | Yield |
---|---|
With hydrogenchloride; oxygen; CuCl2 on calcined alumina at 490℃; Product distribution; several conditions investigated; |
perchloropropene
Conditions | Yield |
---|---|
With potassium hydroxide | |
With pyridine | |
With -base of crystal violet |
pyridine
1,1,1,2,2,3,3-heptachloropropane
A
hydrogenchloride
B
perchloropropene
1,1,2,3-tetrachloro-3,3-difluoropropene
antimonypentachloride
A
1,1,2-trichloro-3,3,3-trifluoropropene
B
1,1,2,3,3-pentachloro-3-fluoropropene
C
perchloropropene
1,1,2,3,3,4,4,5,6,6-decachloro-hexa-1,5-diene
A
1,1,2,2-tetrachloroethylene
B
perchloropropene
Conditions | Yield |
---|---|
at 200 - 210℃; |
heptachloro-butyraldehyde
sodium ethanolate
A
perchloropropene
B
sodium formate
Conditions | Yield |
---|---|
Produkt 5:Perchlorfulven; |
1,1,1,3,3,3-hexachloropropane
A
1-chloro-1,1,3,3,3-pentafluoropropane
B
2H-pentafluoropropene
C
1,1,1,3,3,3-hexafluoropropane
D
perchloropropene
Conditions | Yield |
---|---|
With hydrogen fluoride; chlorine; antimonypentachloride at 80 - 95℃; under 8517.48 - 10069 Torr; | |
With hydrogen fluoride; chromium(III) oxide at 300℃; |
1,1,1,2,2,3,3-heptachloropropane
tetrabutyl-ammonium chloride
perchloropropene
Conditions | Yield |
---|---|
With potassium hydroxide | 237 g (95%) |
1,1,1,2,2,3,3-heptachloropropane
tetra-n-butylphosphonium chloride
perchloropropene
Conditions | Yield |
---|---|
With potassium hydroxide | 239 g (96%) |
Conditions | Yield |
---|---|
With potassium hydroxide | 237 g (95%) |
tetrachloromethane
A
Hexachlorobutadiene
B
perchloropropene
C
hexachlorobenzene
Conditions | Yield |
---|---|
With silica gel In neat (no solvent) byproducts: SiCl4, COCl2; decomposition of streaming CCl4 with high-frequency discharge in a quartz tube; condensation of the reaction mixture at -190°C; mechanism discussed; further products;; determination by IR and MS;; |
Conditions | Yield |
---|---|
Inert atmosphere; Reflux; | 100% |
Conditions | Yield |
---|---|
at 190℃; for 18h; Schlenk technique; Inert atmosphere; | 98% |
In neat (no solvent) refluxing; sublimation (vac.); | |
In neat (no solvent) absence of air and moisture; refluxing; |
perchloropropene
uranium(IV) chloride
Conditions | Yield |
---|---|
In further solvent(s) (N2); standard Schlenk technique; UO2*2H2O was added to hexachloropropene at 190°C; heated at 190°C; UO3*2H2O was carefully added;mixt. was heated at 190°C overnight; cooled to room temp.; filtered; washed (CH2Cl2); dried (vac.); | 98% |
Conditions | Yield |
---|---|
With aluminium trichloride; sulfur dioxide at 90℃; for 48h; | A 85% B n/a |
3-(3-pyridyl)propan-1-ol
2,3,3-trichloroacryloyl chloride
perchloropropene
3-(3-Pyridyl)-1-propyl-2',3',3'-trichloroacrylate
Conditions | Yield |
---|---|
With pyridine; iron(III) chloride | 82% |
perchloropropene
A
1,1,2-trichloro-3,3,3-trifluoropropene
B
1,1,2,3-tetrachloro-3,3-difluoropropene
C
1,1,2,3,3-pentachloro-3-fluoropropene
Conditions | Yield |
---|---|
With antimony(III) fluoride at 170℃; | A 74.2% B n/a C n/a |
With antimony(III) fluoride at 170℃; |
perchloropropene
2,3,4,5,6-pentafluoroaniline
1,1,2,3-tetrachloro-4-(pentafluorophenyl)-4-aza-1,3-butadiene
Conditions | Yield |
---|---|
With aluminium trichloride In fluorobenzene at 70 - 80℃; for 6h; | 73% |
perchloropropene
Conditions | Yield |
---|---|
With sulfur at 170℃; for 24h; | 70% |
Conditions | Yield |
---|---|
With antimonypentachloride In 1,2-dichloro-ethane for 0.166667h; Heating; | 66% |
Conditions | Yield |
---|---|
With antimonypentachloride In dichloromethane 1.) -30 deg C, 30 min, 2.) 23 deg C, 4 h; | 63% |
Conditions | Yield |
---|---|
In dichloromethane 1.) -40 deg C, 30 min, 2.) 23 deg C, 4 h; | 61% |
Conditions | Yield |
---|---|
With antimonypentachloride In 1,2-dichloro-ethane for 0.0833333h; Heating; | 57% |
Conditions | Yield |
---|---|
Inert atmosphere; | 55% |
Conditions | Yield |
---|---|
With antimonypentachloride In dichloromethane 1.) -40 deg C, 10 min; 2.) 23 deg C, 1 h; | 49% |
Conditions | Yield |
---|---|
With iron(III) chloride In 1,1,2,2-tetrachloroethylene | 48.7% |
Conditions | Yield |
---|---|
With antimonypentachloride In dichloromethane 1.) -30 deg C, 30 min, 2.) 23 deg C, 4 h; | 48% |
perchloropropene
1,4-dichloropermethyltetrasilane
hexadecamethyl-2,3,4,5,6,7,8,9,10-octasilabicyclo<4.4.1>undeca-1(11),6(11)-diene
Conditions | Yield |
---|---|
With magnesium In tetrahydrofuran at 50℃; for 4h; | 34% |
Conditions | Yield |
---|---|
With magnesium In tetrahydrofuran at 50℃; for 4h; | 16% |
cis-1,2-Dichloroethylene
perchloropropene
3H-heptachloro-cyclopentene
Conditions | Yield |
---|---|
With aluminium trichloride; dichloromethane at 13 - 15℃; |
Conditions | Yield |
---|---|
With aluminium trichloride; dichloromethane at 9℃; anschliessendes Erhitzen auf Siedetemperatur; |
4-Chloro-3-methylphenol
perchloropropene
3,4,6-trichloro-7-methyl-coumarin
Conditions | Yield |
---|---|
With carbon disulfide; aluminium trichloride anschliessend Behandeln mit wss. Schwefelsaeure; |
Conditions | Yield |
---|---|
With carbon disulfide; aluminium trichloride anschliessend Behandeln mit wss. Schwefelsaeure; | |
Stage #1: p-cresol; perchloropropene With aluminum (III) chloride In carbon disulfide Stage #2: With sulfuric acid; water |
Chlorodifluoromethane
perchloropropene
1,1,2-trichloro-3,3,3-trifluoropropene
Conditions | Yield |
---|---|
With aluminium trichloride at 150℃; dann auf 200grad; |
Chlorodifluoromethane
perchloropropene
1,1,2,3-tetrachloro-3,3-difluoropropene
Conditions | Yield |
---|---|
With aluminium trichloride at 100℃; |
IUPAC Name: 1,1,2,3,3,3-Hexachloroprop-1-ene
Molecular Formula: C3Cl6
Molecular Weight: 248.73g/mol
EINECS: 217-560-9
Transport information: UN 3382 6.1/PG 1
Properties colourless liquid
Density: 1.781 g/cm3
Flash Point: 69.9 °C
Boiling Point: 209.5 °C at 760 mmHg
Freely Rotating Bonds: 0
Polar Surface Area: 0 Å2
Index of Refraction: 1.554
Molar Refractivity: 44.75 cm3
Molar Volume: 139.6 cm3
Polarizability: 17.74 ×10-24 cm3
Surface Tension: 42.6 dyne/cm
Enthalpy of Vaporization: 42.76 kJ/mol
Vapour Pressure: 0.292 mmHg at 25°C
Stability: stable,incompatible with strong oxidizing agents.
Solubility: insoluble in water
The Cas Register Number of Hexachloropropene is 1888-71-7.The chemical synonyms of Hexachloropropene (CAS NO.1888-71-7) are 1,1,1,2,3,3-Hexachloropropene ; 1,1,2,3,3,3-Hexachloro-1-propen ; 1,1,2,3,3,3-Hexachloro-1-propene ; 1,1,2,3,3-Hexachloro-1-propene ; 1-Propene, hexachloro- ; 1-Propene,1,1,2,3,3,3-hexachloro ; 1-Propene,1,1,2,3,3,3-hexachloro- ; Hexachloro-1-propene .The molecular structure of Hexachloropropene (CAS NO.1888-71-7) is.
Hexachloropropene (CAS NO.1888-71-7) is used as plasticizer and hydraulic fluid .And it also is used in organic synthesis.
Its raw materials are Potassium ethylate and 1,1,1,2,2,3,3-Heptachloropropane .
1. | mmo-sat 15 µmol/L | MUREAV Mutation Research. 170 (1986),1. | ||
2. | ihl-rat LC50:425 ppm/30M | XEURAQ U.S. Atomic Energy Commission, University of Rochester, Research and Development Reports. (Rochester, NY) MDDC-1715 . | ||
3. | ipr-rat LD50:400 mg/kg | XEURAQ U.S. Atomic Energy Commission, University of Rochester, Research and Development Reports. (Rochester, NY) MDDC-1715 . | ||
4. | ihl-mus LCLo:300 ppm/30M | XEURAQ U.S. Atomic Energy Commission, University of Rochester, Research and Development Reports. (Rochester, NY) MDDC-1715 . | ||
5. | ipr-mus LDLo:64 mg/kg | CBCCT* “Summary Tables of Biological Tests“ National Research Council Chemical-Biological Coordination Center. 1 (1949),46. | ||
6. | ihl-rbt LCLo:85 ppm/30M | XEURAQ U.S. Atomic Energy Commission, University of Rochester, Research and Development Reports. (Rochester, NY) MDDC-1715 . |
Reported in EPA TSCA Inventory.
A poison by inhalation and intraperitoneal routes. A powerful irritant. Mutation data reported. When heated to decomposition it emits toxic fumes of Cl−. See also CHLORINATED HYDROCARBONS, ALIPHATIC.
Hazard Codes: T
Risk Statements: 23-36/37/38
R23: Toxic by inhalation.
R36/37/38: Irritating to eyes, respiratory system and skin.
Safety Statements: 26-36/37/39-45
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39: Wear suitable protective clothing, gloves and eye/face protection.
S45: In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
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