tris-2,2'-bipyridyl ruthenium(III) ion
H2O(1,4,8,11-tetraazacyclotetradecane)CoPr(2+)
1-Chloropropane
Conditions | Yield |
---|---|
With chloropentamminecobalt(III)(2+) Kinetics; reaction of Ru(bpy)3(3+) with excess Co-compound in presence of Co(NH3)5Cl(2+);; | 100% |
propyl 2-chloro-1,1-diethyl carbamate
A
1-Chloropropane
B
4,4-di-2-oxazolidone
Conditions | Yield |
---|---|
at 150℃; for 1h; | A n/a B 98% |
propyloxy(diphenyl)-λ6-sulfanenitrile
A
1-Chloropropane
B
S,S-diphenylsulphoximine
Conditions | Yield |
---|---|
With hydrogenchloride In [D3]acetonitrile at 20℃; for 0.5h; | A 98% B n/a |
tetrachloromethane
di-n-propylmercury
B
1-Chloropropane
C
chloroform
D
n-propylmercury(II) chloride
Conditions | Yield |
---|---|
In neat (no solvent) 150°C, 60 h; further products; | A <1 B 96% C >99 D 5% E 95% |
Conditions | Yield |
---|---|
With hydrogenchloride; tetrabutylphosphonium ion; silica gel at 170℃; under 760 Torr; | A 94% B 5 % Chromat. |
Conditions | Yield |
---|---|
With chloro-trimethyl-silane; dimethyl sulfoxide for 0.166667h; | 93% |
With priphenylchlorophosphonium phosphorodichloridate at 20℃; Arbuzov reaction; | 88% |
With allyltriphenoxyphosphonium chloride at 20℃; | 60% |
tripropyl phosphorotrithioite
A
tripropyl tetrathiophosphate
B
1-Chloropropane
C
propyl phosphorodichloridothioite
D
dipropyl phosphorochloridodithioite
Conditions | Yield |
---|---|
With chlorine for 0.333333h; Product distribution; | A 93% B 64% C 0.9 g D 45% |
Conditions | Yield |
---|---|
With phosphorus trichloride at 0 - 50℃; for 50h; | A n/a B 93% |
Conditions | Yield |
---|---|
With 2-chloro-4,6-dimethoxy-1 ,3,5-triazine In toluene Reflux; | 90% |
tripropyl phosphorotrithioite
A
tripropyl tetrathiophosphate
B
1-Chloropropane
C
propyl phosphorodichloridothioite
Conditions | Yield |
---|---|
With phosphorus pentachloride at 80℃; for 0.75h; Product distribution; | A 84% B 73% C 35% |
1,1,2,2,3,3,4,4-Octafluoro-5,5-bis-propylsulfanyl-pentane
A
1-Chloropropane
B
1,1-Dichloro-2,2,3,3,4,4,5,5-octafluoro-1-propylsulfanyl-pentane
Conditions | Yield |
---|---|
With chlorine In tetrachloromethane at 10℃; for 3h; | A n/a B 80% |
tri-n-propyl phosphite
2,2,2-trichloro-N-methylacetimidoyl chloride
A
1-Chloropropane
B
C15H31Cl2NO6P2
Conditions | Yield |
---|---|
In toluene for 2h; Heating; | A n/a B 75% |
tri-n-propyl phosphite
N-ethyl-2,2,2-trichloro-acetimidoyl chloride
A
1-Chloropropane
B
{2,2-Dichloro-1-[(dipropoxy-phosphoryl)-ethyl-amino]-vinyl}-phosphonic acid dipropyl ester
Conditions | Yield |
---|---|
In toluene for 2h; Heating; | A n/a B 71% |
Vinyliden-methylphosphonsaeure-dipropylester
trichloro(o-phenylenedioxy)phosphorane
A
o-phenylene chlorophosphate
B
1-Chloropropane
C
propyl propadienylchlorophosphonate
Conditions | Yield |
---|---|
at 20℃; for 24h; | A n/a B n/a C 66% |
1-(2-chlorophenyl)ethanone
C11H14ClN
A
1-Chloropropane
B
2-(2'-chlorophenyl)-4-methylquinoline
Conditions | Yield |
---|---|
In toluene at 150℃; for 48h; | A n/a B 64% |
(3,4-dihydro-2H-pyran-5-yl)phosphonous dichloride
butan-1-ol
A
1-Chloropropane
Conditions | Yield |
---|---|
In diethyl ether Ambient temperature; | A n/a B 61.3% |
propan-1-ol
(3,4-dihydro-2H-pyran-5-yl)phosphonous dichloride
A
1-Chloropropane
Conditions | Yield |
---|---|
In diethyl ether Ambient temperature; | A n/a B 60.2% |
tetrachloromethane
oxygen
di-n-propylmercury
B
1-Chloropropane
C
chloroform
D
n-propylmercury(II) chloride
Conditions | Yield |
---|---|
In neat (no solvent) 100°C, 60 h; further products; | A 5% B 58% C 39% D 50% E 40% |
propan-1-ol
(4,5-dihydro-3-furyl)phosphonous dichloride
A
1-Chloropropane
Conditions | Yield |
---|---|
With triethylamine In diethyl ether at -20 - -15℃; for 0.333333h; | A n/a B 54.4% |
3-(phenylsulfonyl)propyl chloride
A
1-Chloropropane
B
(cyclopropylsulfonyl)benzene
C
1,6-dichlorohexane
Conditions | Yield |
---|---|
With sodium amalgam In benzene for 6h; Heating; | A 17% B 53% C 13% |
propan-1-ol
<2-(2-chloroethoxy)vinyl>phosphonous dichloride
A
1-Chloropropane
Conditions | Yield |
---|---|
With triethylamine In diethyl ether at -20 - -15℃; for 0.333333h; | A n/a B 40% |
bis-(4-methoxyphenyltelluro)methane
A
4-Methylanisole
B
1-Chloropropane
C
4,4'-Dimethoxybiphenyl
D
bis(4-methoxyphenyl)telluride
G
4-methoxy-phenol
Conditions | Yield |
---|---|
In dichloromethane at 20℃; Mechanism; | A n/a B n/a C n/a D n/a E 4% F 10% G n/a |
pyridine
(Propoxy)thiocarbonylchlorid
A
carbon oxide sulfide
B
1-Chloropropane
quinoline
(Propoxy)thiocarbonylchlorid
A
carbon oxide sulfide
B
1-Chloropropane
Conditions | Yield |
---|---|
at 29℃; |
Conditions | Yield |
---|---|
With hydrogenchloride; aluminum oxide at 420℃; |
Conditions | Yield |
---|---|
sowie Isomerisierung bei Siedetemperatur; |
tetrachloromethane
dibutyryl peroxide
A
1-Chloropropane
B
hexachloroethane
Conditions | Yield |
---|---|
With hydrogenchloride; hydrogen bromide Einwirkung von stillen elektrischen Entladungen; | |
With hydrogenchloride; hydrogen bromide Einwirkung von stillen elektrischen Entladungen; |
1-(2-chloro-ethylsulfanyl)-2-propylsulfanyl-ethane
A
1,4-Dithiane
B
1-Chloropropane
Conditions | Yield |
---|---|
beim Erhitzen; |
Conditions | Yield |
---|---|
With chromium nickel; chlorine at 600℃; | |
With chlorine; tetraethyllead(IV) at 136 - 140℃; | |
With iodine Chlorierung; |
1-methyl-1H-imidazole
1-Chloropropane
1-methyl-3-propyl-1H-imidazolium chloride
Conditions | Yield |
---|---|
at 70℃; for 48h; | 99% |
at 170℃; Microwave irradiation; | 95% |
im Rohr; |
Conditions | Yield |
---|---|
With potassium carbonate; potassium iodide In acetone a) RT, 24 h, b) reflux, 120 h; | 99% |
1-Chloropropane
bis(4-amino-3-nitrophenyl) disulfide
1-amino-2-nitro-4-n-propylthiobenzene
Conditions | Yield |
---|---|
Stage #1: bis(4-amino-3-nitrophenyl) disulfide With sodiumsulfide nonahydrate In methanol for 0.5h; Stage #2: 1-Chloropropane In methanol at 55℃; Temperature; | 98.32% |
7-hydroxy-2,2-dimethyl-chroman-4-one
1-Chloropropane
2,2-Dimethyl-7-propoxy-chroman-4-one
Conditions | Yield |
---|---|
With potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 80℃; for 7h; | 96% |
Conditions | Yield |
---|---|
at 180℃; under 2250.23 Torr; for 0.5h; Microwave irradiation; Inert atmosphere; neat (no solvent); | 96% |
Conditions | Yield |
---|---|
at 40 - 55℃; for 6h; | 95.3% |
1-Chloropropane
2-amino-1-(4-(methylsulfonyl)phenyl)ethanone
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 5 - 100℃; for 6h; Reagent/catalyst; | 95.3% |
Conditions | Yield |
---|---|
With C30H38Cl2Ir2N4 In dimethyl sulfoxide at 50℃; for 5h; | 95% |
With oxygen; kieselguhr; copper(l) chloride In dichloromethane for 1.5h; Oxidation; Heating; | 91% |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In propan-1-ol at 40℃; for 1.5h; | 95% |
1-Chloropropane
1,8-diazabicyclo[5.4.0]undec-7-ene
1-propyl-2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepin-1-ium chloride
Conditions | Yield |
---|---|
for 9h; Reflux; | 95% |
Conditions | Yield |
---|---|
Stage #1: 1-Chloropropane With magnesium; 1,2-dibromomethane In toluene at 60℃; for 3h; Inert atmosphere; Stage #2: propoxycarbonyl chloride With aluminum (III) chloride; manganese(ll) chloride In toluene at 0 - 20℃; for 2.25h; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
With NPs-Fe3O4(at)SiO2(at)[PrMIM]PW In acetonitrile at 50℃; Reagent/catalyst; Solvent; Temperature; | 95% |
1-Chloropropane
(S)-4,5,6,7-tetrahydrobenzo[d]thiazol-2,6-diamine
pramipexole
Conditions | Yield |
---|---|
With NPs-Fe3O4(at)SiO2(at)[PrMIM]PW In acetonitrile at 50℃; Reagent/catalyst; | 95% |
Conditions | Yield |
---|---|
at 70℃; Temperature; | 94.7% |
Conditions | Yield |
---|---|
With Rh(PPh3)3Cl In dichloromethane at 150℃; for 3h; | 94% |
1-Chloropropane
triphenylphosphine
A
Propylbenzene
B
diphenylphosphinopropane
Conditions | Yield |
---|---|
Stage #1: triphenylphosphine With lithium In tetrahydrofuran at 20℃; for 3h; Inert atmosphere; Stage #2: 1-Chloropropane In tetrahydrofuran at 5 - 50℃; for 6.25h; | A 93.5% B 91.6% |
Conditions | Yield |
---|---|
In toluene at 180℃; for 0.5h; Inert atmosphere; Microwave irradiation; | 93% |
In acetone |
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-5-methoxytryptamine With sodium hydride at 100℃; Metallation; Stage #2: 1-Chloropropane In N,N-dimethyl-formamide at 20℃; Alkylation; Further stages.; | 93% |
Conditions | Yield |
---|---|
With NPs-Fe3O4(at)SiO2(at)[PrMIM]PW In acetonitrile at 50℃; | 93% |
Conditions | Yield |
---|---|
With 1,1'-(hexane-1,6-diyl)bis(1,8-diazabicyclo[5.4.0]undec-7-enium) dichlorine In ethanol; water at 70℃; for 2h; Green chemistry; | 93% |
Conditions | Yield |
---|---|
With 1,1'-(hexane-1,6-diyl)bis(1,8-diazabicyclo[5.4.0]undec-7-enium) dichlorine In ethanol; water at 70℃; for 2h; Green chemistry; | 93% |
1-Chloropropane
carbon dioxide
ethylamine
1-propyl ethylcarbamate
Conditions | Yield |
---|---|
With choline chloride * 2ZnCl2 at 20℃; under 760.051 Torr; for 2h; Green chemistry; | 93% |
Molecular Structure:
Molecular Formula: C3H7Cl
Molecular Weight: 78.5407
IUPAC Name: 1-Chloropropane
Synonyms of Propyl chloride (CAS NO.540-54-5): 1-Chloropropane ; 4-01-00-00189 (Beilstein Handbook Reference) ; AI3-28788 ; BRN 1730771 ; CCRIS 9257 ; EINECS 208-749-7 ; HSDB 5681 ; N-Propyl chloride ; Propane, 1-chloro- ; Propyl chloride [UN1278] [Flammable liquid] ; UN1278
CAS NO: 540-54-5
Classification Code: Organics ; Alkyl Chlorides ; Monofunctional & alpha,omega-Bifunctional Alkanes ; Monofunctional Alkanes
Melting point: -123 °C
Index of Refraction: 1.381
Molar Refractivity: 20.79 cm3
Molar Volume: 89.4 cm3
Surface Tension: 20.3 dyne/cm
Density: 0.878 g/cm3
Enthalpy of Vaporization: 27.18 kJ/mol
Boiling Point: 46.8 °C at 760 mmHg
Vapour Pressure: 343 mmHg at 25°C
Propyl chloride (CAS NO.540-54-5) is used in organic synthesis, pesticide, pharmaceutical intermediate and used as chemical intermediate for n-propylamine (former use).
Product Categories about Propyl chloride (CAS NO.540-54-5) are Organics;Alkyl Chlorides;Monofunctional & alpha,omega-Bifunctional Alkanes;Monofunctional Alkanes.
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
rat | LD50 | oral | > 2gm/kg (2000mg/kg) | Mutation Research. Vol. 101, Pg. 321, 1982. |
Reported in EPA TSCA Inventory.
Hazard Codes of Propyl chloride (CAS NO.540-54-5): F,Xn
Risk Statements: 11-20/21/22
R11: Highly flammable.
R20/21/22: Harmful by inhalation, in contact with skin and if swallowed.
Safety Statements: 9-29
S9: Keep container in a well-ventilated place.
S29: Do not empty into drains.
RIDADR: UN 1278 3/PG 2
WGK Germany: 3
RTECS: TX4400000
HazardClass: 3.1
PackingGroup: II
A moderately poisonous irritant to skin, eyes, and mucous membranes. Narcotic in high concentrations. Flammable liquid and dangerous fire hazard when exposed to heat, flame, or oxidizers. Moderately explosive when exposed to flame. Keep away from heat and open flame; can react vigorously with oxidizing materials. To fight fire, use CO2, dry chemical. When heated to decomposition it emits toxic fumes of Cl−. See also CHLORINATED HYDROCARBONS, ALIPHATIC.
DOT Classification: 3; Label: Flammable Liquid
1. Storage: Keep away from heat, sparks, and flame. Keep away from sources of ignition. Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.
2. Handling: Wash thoroughly after handling. Use only in a well ventilated area. Ground and bond containers when transferring material. Avoid contact with eyes, skin, and clothing. Empty containers retain product residue, (liquid and/or vapor), and can be dangerous. Keep container tightly closed. Avoid contact with heat, sparks and flame. Avoid ingestion and inhalation. Do not pressurize, cut, weld, braze, solder, drill, grind, or expose empty containers to heat, sparks or open flames.
3. Personal Protection: Eyes: Wear appropriate protective eyeglasses or chemical safety goggles as described by OSHA's eye and face protection regulations in 29 CFR 1910.133 or European Standard EN166. Skin: Wear appropriate protective gloves to prevent skin exposure. Clothing: Wear appropriate protective clothing to prevent skin exposure.
4. Fire Fighting: Do not extinguish fire unless flow can be stopped. Use water in flooding quantities as fog. Solid streams of water may spread fire. Cool all affected containers with flooding quantities of water. Apply water from as far a distance as possible. Use foam, dry chemical, or carbon dioxide.
5. Reactivity Profile: 1-Chloropropane presents a dangerous fire risk. May be incompatible with strong oxidizing and reducing agents. Incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides.
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