1,2-Dichloropropane
1,1,2-trichloropropane
Conditions | Yield |
---|---|
With aluminum (III) chloride; sulfuryl dichloride at 60℃; for 1h; Reagent/catalyst; Solvent; Inert atmosphere; | 33% |
With chlorine im Sonnenlichte; | |
With antimonypentachloride |
1,2-Dichloropropane
A
1,2,2-trichloropropane
B
1,1,2,2-tetrachloropropane
C
1,1,2-trichloropropane
D
1,2,3-trichloropropane
E
1,2,2,3-tetrachloropropane
F
1,1,2,3-tetrachloropropane
Conditions | Yield |
---|---|
With sulfuryl dichloride at 55 - 60℃; | A 18% B 13.2% C 8.9% D 20.3% E 10.1% F 15.6% |
With sulfuryl dichloride; 2,2'-azobis(isobutyronitrile) at 55 - 60℃; | A 19.7% B 17.8% C 6.5% D 14.8% E 11.8% F 15.6% |
With sulfuryl dichloride at 55 - 60℃; Product distribution / selectivity; | |
With chlorine; dimethyl 2,2'-azobis(isobutyrate) In tetrachloromethane at 70℃; under 8517.48 Torr; for 32h; Product distribution / selectivity; Inert atmosphere; |
propene
1,1,2-trichloropropane
Conditions | Yield |
---|---|
With chlorine at 52 - 65℃; im Dunkeln; |
1,2-Dichloropropane
A
1,1,2-trichloropropane
B
1,2,3-trichloropropane
Conditions | Yield |
---|---|
With Iodine monochloride at 160℃; | |
With iron(III) chloride; chlorine at 100℃; under 7224.57 Torr; for 5h; Product distribution / selectivity; Inert atmosphere; | |
With aluminum (III) chloride; sulfuryl dichloride; iodine at 55 - 60℃; Reagent/catalyst; | |
With aluminum (III) chloride; sulfuryl dichloride at 55 - 60℃; for 0.5h; | |
With aluminum (III) chloride; chlorine In tetrachloromethane at 60℃; for 1h; Inert atmosphere; Overall yield = 22 %; |
Conditions | Yield |
---|---|
With chlorine | |
With antimonypentachloride |
Conditions | Yield |
---|---|
With chlorine im Sonnenlichte; | |
With chlorine | |
With antimonypentachloride |
1,2-Dichloropropane
antimonypentachloride
1,1,2-trichloropropane
chloroform
1,1-dichloropropane
antimonypentachloride
1,1,2-trichloropropane
Conditions | Yield |
---|---|
bei Siedetemperatur; 1.2-dichloro-propane; |
aluminium trichloride
1,2-Dichloropropane
chlorine
A
1,2,2-trichloropropane
B
1,1,2-trichloropropane
propene
chlorine
A
1,2,2-trichloropropane
B
1,2-Dichloropropane
C
1,1,2-trichloropropane
1,2-Dichloropropane
chlorine
A
1,1,2-trichloropropane
B
1,2,3-trichloropropane
Conditions | Yield |
---|---|
at 50 - 55℃; im UV-Licht.Irradiation; 1.2-dichloro-propane; |
sulfuryl dichloride
1,2-Dichloropropane
dilauryl peroxide
A
1,2,2-trichloropropane
B
1,1,2-trichloropropane
C
1,2,3-trichloropropane
Conditions | Yield |
---|---|
Product distribution; 1.2-dichloro-propane; |
sulfuryl dichloride
1,2-Dichloropropane
dibenzoyl peroxide
A
1,2,2-trichloropropane
B
1,1,2-trichloropropane
C
1,2,3-trichloropropane
Conditions | Yield |
---|---|
Product distribution; 1.2-dichloro-propane; |
propene
chlorine
A
1,2,2-trichloropropane
B
1,2-Dichloropropane
C
1,1,2-trichloropropane
D
1,2,3-trichloropropane
Conditions | Yield |
---|---|
at 52 - 66℃; in Gegenwart von fluessigen Anteilen des Reaktionsprodukts; aus 3 Mol Propylen und l Mol Chlor im Dunkeln; |
propene
chlorine
A
1,2,2-trichloropropane
B
1,2-Dichloropropane
C
1,1,2-trichloropropane
D
1,2,3-trichloropropane
Conditions | Yield |
---|---|
at 52 - 66℃; aus 3 Mol Propylen und l Mol Chlor im Dunkeln; |
propene
chlorine
A
1,2,2-trichloropropane
B
1,2-Dichloropropane
C
1,1,2-trichloropropane
D
1,2,3-trichloropropane
Conditions | Yield |
---|---|
at 52 - 66℃; aus 3 Mol Propylen und l Mol Chlor im Dunkeln; |
1,3-Dichloropropane
1-chloro-3-hydroxypropane
A
glycidyl methyl ether
B
1,2-Epoxyhexane
C
2,3-Dichloroprop-1-ene
D
2-chloroallyl alcohol
E
1,2,2-trichloropropane
F
1,2-Dichloropropane
G
(Z)-1,3-dichloropropene
H
1,2,3-trichloro-1-propene
I
(1Z)-1,2,3-trichloroprop-1-ene
J
1,3,3-trichloro-propene
K
1t,3,3-trichloro-propene
L
chlorodibromomethane
M
1,1,2-trichloropropane
N
2,3-Dichloro-1-propanol
O
1,3-Dichloro-2-propanol
P
1,2,3-trichloropropane
Q
3,3-dichloropropene
R
3,3-dichloroallyl chloride
S
acetaldehyde
T
allyl alcohol
U
hydroxy-2-propanone
V
chloroacetone
W
cyclopentanone
X
chlorobenzene
Y
isopropyl alcohol
Z
3-monochloro-1,2-propanediol
[
acrolein
\
epichlorohydrin
]
(E)-1,3-dichloro-prop-1-ene
Conditions | Yield |
---|---|
With sodium hydroxide; water at 45 - 62.4℃; under 112.511 - 750.075 Torr; Product distribution / selectivity; |
1,2-Dichloropropane
A
1,2,2-trichloropropane
B
1,1,2,2-tetrachloropropane
C
1,1,2-trichloropropane
D
1,2,3-trichloropropane
E
1,2,2,3-tetrachloropropane
F
1,1,2,3-tetrachloropropane
G
1,1,2,3,3-pentachloropropane
Conditions | Yield |
---|---|
With sulfuryl dichloride; 2,2'-azobis(isobutyronitrile) at 55 - 60℃; |
1,2-Dichloropropane
A
1,2,2-trichloropropane
B
1,1,2,2-tetrachloropropane
C
1,1,2-trichloropropane
D
1,2,3-trichloropropane
E
1,1,2,3-tetrachloropropane
Conditions | Yield |
---|---|
With chlorine; 2,2'-azobis-(2,4-dimethylvaleronitrile) In tetrachloromethane at 70℃; under 6723.1 Torr; for 3.26667h; Product distribution / selectivity; Inert atmosphere; |
Conditions | Yield |
---|---|
With aluminum (III) chloride; sulfuryl dichloride at 55 - 60℃; |
1,2-Dichloropropane
A
1,1,2-trichloropropane
B
1,2,3-trichloropropane
C
1,1,2,2,3-pentachloropropane
Conditions | Yield |
---|---|
With aluminum (III) chloride; sulfuryl dichloride; sodium iodate at 60℃; for 4h; | A 1.4 g B 0.8 g C 2.3 g |
1,2-Dichloropropane
A
1,1,2-trichloropropane
B
1,2,3-trichloropropane
C
1,2,2,3-tetrachloropropane
D
1,1,2,2,3-pentachloropropane
Conditions | Yield |
---|---|
With aluminum (III) chloride; sulfuryl dichloride; iodine at 55 - 70℃; for 7h; Inert atmosphere; |
1,2-Dichloropropane
A
1,1,2-trichloropropane
B
1,2,3-trichloropropane
C
1,1,2,2,3-pentachloropropane
D
1,1,2,2,3,3-hexachloropropane
Conditions | Yield |
---|---|
With aluminum (III) chloride; iodine; chlorine In dichloromethane at 70℃; under 7224.57 - 7741.73 Torr; for 2h; Sealed tube; |
Conditions | Yield |
---|---|
With hydrogen fluoride; mercury(II) oxide at 100℃; |
Conditions | Yield |
---|---|
With hydrogen fluoride; mercury(II) oxide at 100℃; |
Conditions | Yield |
---|---|
With sodium hydroxide | |
With benzyltrimethylammonium chloride; sodium hydroxide In water at 70℃; for 4h; | |
With sodium hydroxide |
1,1,2-trichloropropane
1,1,2,3-tetrachloropropane
Conditions | Yield |
---|---|
With aluminium trichloride; chlorine |
1,1,2-trichloropropane
carbon monoxide
benzene
A
1,1-diphenyl-1-propene
B
(±)-2-methyl-2-phenyl-2,3-dihydro-1H-inden-1-one
Conditions | Yield |
---|---|
With aluminium trichloride at 24 - 27℃; for 3h; |
1,1,2-trichloropropane
antimonypentachloride
1,1,1,2,2-pentachloropropane
Conditions | Yield |
---|---|
at 155℃; |
1,1,2-trichloropropane
hydrogen fluoride
A
2-chloro-1,1-difluoro-propane
B
1,2-dichloro-1-fluoro-propane
C
1,1,2-trifluoropropane
Conditions | Yield |
---|---|
at 100℃; |
IUPAC Name: 1,1,2-Trichloropropane
Synonyms: 1,1,2-Trichloropropane ;propane, 1,1,2-trichloro-
CAS NO:598-77-6
Molecular Formula of 1,1,2-Trichloropropane(CAS NO.598-77-6):C3H5Cl3
Molecular Weight of 1,1,2-Trichloropropane(CAS NO.598-77-6):147.43
Molecular Structure of 1,1,2-Trichloropropane(CAS NO.598-77-6):
EINECS: 209-951-8
Index of Refraction:1.45
Surface Tension: 28.7 dyne/cm
Density: 1.305 g/cm3
Flash Point: 44.3 °C
Enthalpy of Vaporization: 34.82 kJ/mol
Boiling Point: 125.3 °C at 760 mmHg
Vapour Pressure: 14.8 mmHg at 25°C
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
rabbit | LD50 | skin | 14100uL/kg (14.1mL/kg) | AMA Archives of Industrial Hygiene and Occupational Medicine. Vol. 10, Pg. 61, 1954. | |
rat | LC50 | inhalation | 2000ppm/4H (2000ppm) | AMA Archives of Industrial Hygiene and Occupational Medicine. Vol. 10, Pg. 61, 1954. | |
rat | LD50 | oral | 1230mg/kg (1230mg/kg) | AMA Archives of Industrial Hygiene and Occupational Medicine. Vol. 10, Pg. 61, 1954. |
Reported in EPA TSCA Inventory.
Moderately toxic by ingestion. Mildly toxic by inhalation and skin contact. A skin and severe eye irritant. When heated to decomposition it emits toxic fumes of Cl−. See also CHLORINATED HYDROCARBONS, ALIPHATIC.
Risk Statements 20/21/22-36/37/38
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements 26-36/37/39
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.
RTECS TZ8925000
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