Conditions | Yield |
---|---|
With thionyl chloride In hexane for 3h; Heating; | 95% |
With pyridine; phosgene at 55℃; for 1h; Reagent/catalyst; Temperature; | 95.4% |
With thionyl chloride In N,N-dimethyl-formamide at 85℃; for 2h; | 85% |
LACTIC ACID
2-chloropropionyl chloride
Conditions | Yield |
---|---|
With pyridine; thionyl chloride | |
With phosphorus pentachloride; water |
Conditions | Yield |
---|---|
With iodine; chlorine | |
With sulfuryl dichloride; iodine |
propionyl chloride
A
2-chloropropionyl chloride
B
2-chloropropionyl chloride
Conditions | Yield |
---|---|
With chlorine at 0 - 5℃; Irradiation.unter UV-Bestrahlung; | |
With sulfuryl dichloride; dibenzoyl peroxide | |
With sulfuryl dichloride; dibenzoyl peroxide |
1,1,1-trichloropropan-2-ol
A
2-chloropropionyl chloride
B
1,1,2-trichloropropene
C
1,1,1-trichloroisopropyl α-chloropropionate
Conditions | Yield |
---|---|
With phosphorus pentoxide Heating; Yield given. Yields of byproduct given; | |
With phosphorus pentoxide Product distribution; Heating; | |
With phosphorus pentoxide Heating; Yield given; |
sulfuryl dichloride
iodine
propionyl chloride
2-chloropropionyl chloride
2-chloropropionyl chloride
N,N'-diisopropyl selenourea
Conditions | Yield |
---|---|
With pyridine In tetrahydrofuran at 0℃; | 100% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; | 100% |
3,4-dihydro-2(1H)-quinolone
2-chloropropionyl chloride
6-(2-chloropropanoyl)-3,4-dihydroquinolin-2(1H)-one
Conditions | Yield |
---|---|
With aluminium trichloride In carbon disulfide at 50℃; for 2h; Friedel-Crafts reaction; | 100% |
Stage #1: 2-chloropropionyl chloride With carbon disulfide; aluminum (III) chloride for 0.25h; Inert atmosphere; Cooling with ice; Stage #2: 3,4-dihydro-2(1H)-quinolone for 2.75h; Reflux; | 91% |
aluminium trichloride In carbon disulfide | |
AlCl3 In CS2 | 27.7 g (91%) |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 16h; | 100% |
2-chloropropionyl chloride
1-t-Butoxycarbonylpiperazine
tert-butyl 4-(2-chloropropanoyl)piperazine-1-carboxylate
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0℃; for 1h; | 100% |
2-chloropropionyl chloride
Conditions | Yield |
---|---|
In toluene at 100℃; for 2h; | 100% |
2-chloropropionyl chloride
2-benzylamino-2-methyl-1-propanol
Conditions | Yield |
---|---|
With triethylamine In isopropyl alcohol at 0 - 20℃; | 100% |
With triethylamine In isopropyl alcohol at 0 - 20℃; | |
With triethylamine In isopropyl alcohol at 0 - 20℃; | |
With triethylamine In isopropyl alcohol at 0 - 20℃; for 0.5h; |
2-chloropropionyl chloride
Conditions | Yield |
---|---|
With triethylamine In isopropyl alcohol at 0 - 20℃; for 0.5h; | 100% |
With triethylamine In isopropyl alcohol at 0 - 20℃; | |
With triethylamine In isopropyl alcohol at 0 - 20℃; for 0.5h; | |
With triethylamine In isopropyl alcohol at 0℃; Inert atmosphere; |
2-chloropropionyl chloride
(2R)-2-(benzylamino)butane-1,4-diol
Conditions | Yield |
---|---|
With triethylamine In isopropyl alcohol at 0℃; for 0.166667h; | 100% |
Conditions | Yield |
---|---|
Stage #1: 2-amino-4-chloro-benzoic acid methyl ester With potassium carbonate In tetrahydrofuran at 20℃; for 0.166667h; Stage #2: 2-chloropropionyl chloride In tetrahydrofuran at 0 - 20℃; | 100% |
Conditions | Yield |
---|---|
With 1-methyl-1H-imidazole; N,N,N,N,-tetramethylethylenediamine; potassium carbonate In acetonitrile at 0 - 5℃; for 1h; | 99% |
In dichloromethane at 0 - 5℃; | 95.5% |
In acetone at 20℃; for 4h; | 93.2% |
2-chloropropionyl chloride
p-toluidine
2-chloro-N-(4-methyl-phenyl)propionamide
Conditions | Yield |
---|---|
In toluene at 120℃; for 1h; | 99% |
With N-ethyl-N,N-diisopropylamine In ethyl acetate at 25℃; for 5h; Reagent/catalyst; Solvent; Temperature; Flow reactor; | 93% |
With sodium carbonate In water; toluene at 20℃; for 2.5h; | 89.9% |
2-chloropropionyl chloride
4-chloro-aniline
2-chloro-N-(4-chloro-phenyl)propionamide
Conditions | Yield |
---|---|
In toluene for 1h; Heating; | 99% |
In toluene at 120℃; for 1h; | 98% |
In N,N-dimethyl acetamide at 0 - 50℃; for 96h; | 86% |
In benzene Reflux; | |
With pyridine In chloroform at 20℃; for 12h; |
2-chloropropionyl chloride
4-bromo-aniline
N-(4-bromophenyl)-2-chloropropanamide
Conditions | Yield |
---|---|
In toluene at 120℃; for 1h; | 99% |
In toluene Heating; | |
With pyridine In chloroform at 20℃; for 12h; |
2-chloropropionyl chloride
3,4-difluoroaniline
2-chloro-N-(3,4-difluoro-phenyl)-propionamide
Conditions | Yield |
---|---|
In toluene at 120℃; for 1h; | 99% |
In toluene Heating; |
tert-butyl 6-amino-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indole-2-carboxylate
2-chloropropionyl chloride
tert-butyl 6-[(3-chloropropanoyl)amino]-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indole-2-carboxylate
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; dmap In benzene | 99% |
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
2-chloropropionyl chloride
6-(2-chloropropanoyl)-2H-1,4-benzoxazin-3(4H)-one
Conditions | Yield |
---|---|
With aluminum (III) chloride In 1,2-dichloro-ethane at 20℃; for 12h; | 99% |
2-chloropropionyl chloride
2-(benzylamino)-2-methyl-propan-1,3-diol
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; | 99% |
With triethylamine In dichloromethane at 0℃; for 0.166667h; | 99% |
With triethylamine In dichloromethane at 0℃; Temperature; | |
With triethylamine In dichloromethane at 0 - 20℃; for 0.166667h; Time; Concentration; |
2-chloropropionyl chloride
Conditions | Yield |
---|---|
In toluene at 100℃; for 2h; | 99% |
In toluene at 100℃; for 2h; | 99% |
4-nitro-phenol
2-chloropropionyl chloride
4-nitrophenyl 2-chloropropanoate
Conditions | Yield |
---|---|
With pyridine In tetrahydrofuran for 0.5h; | 98.5% |
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate In dichloromethane; water for 0.5h; | 38% |
In pyridine; dichloromethane Ambient temperature; |
2-chloropropionyl chloride
4-fluoroaniline
N-4'-fluorophenyl-2-chloropropanamide
Conditions | Yield |
---|---|
In toluene at 120℃; for 1h; | 98.5% |
In toluene Heating; | |
With triethylamine In dichloromethane at 20℃; for 4h; | |
With triethylamine In dichloromethane at 0 - 20℃; for 4.33h; Inert atmosphere; |
2-chloropropionyl chloride
3-amino-2-imino-3,4-dihydro-2H-1,3-benzothiazin-4-one
2-(1-Chloroethyl)-1,2,4-triazolo<5,1-b><1,3>benzothiazin-9-one
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide for 2h; Heating; | 98% |
Conditions | Yield |
---|---|
In benzene for 1h; Heating; | 98% |
2-chloropropionyl chloride
4-methoxy-aniline
2-chloro-N-(4-methoxy-phenyl)propionamide
Conditions | Yield |
---|---|
In toluene at 120℃; for 1h; | 98% |
With triethylamine In dichloromethane at 0 - 20℃; for 4.33h; Inert atmosphere; | 97% |
In N,N-dimethyl acetamide at 0 - 50℃; for 96h; | 81% |
Conditions | Yield |
---|---|
In 1,4-dioxane at 20℃; for 1h; | 98% |
Conditions | Yield |
---|---|
With aluminum (III) chloride In dichloromethane at 5 - 25℃; for 19h; Friedel-Crafts Alkylation; Inert atmosphere; regioselective reaction; | 98% |
Spiro-<2,3-dihydro-4H-1,3-benzoxazine-1,2'-cyclohexan>-4-one
2-chloropropionyl chloride
Conditions | Yield |
---|---|
With pyridine In toluene at 30 - 50℃; for 5h; | 97.4% |
With pyridine In chlorobenzene at 50℃; for 8h; Reagent/catalyst; Solvent; Temperature; Inert atmosphere; | 95% |
With pyridine In chloroform at 50℃; for 8h; Reagent/catalyst; Solvent; Temperature; Inert atmosphere; | 95% |
With propylamine In toluene at 10 - 75℃; Reagent/catalyst; Green chemistry; |
The 2-Chloropropionyl chloride, with the cas registry number 7623-09-8, is a kind of clear colorless to light yellow liquid, with the product categories including Acid Halides; Carbonyl Compounds; Organic Building Blocks. Then it is a kind of chemical which is incompatible with strong oxidizing agents,strong bases, amines,alcohols. As to its usage, it could be used as the intermediate in the pharmaceutic, dyes, pesticide and also as the crops protective agent. What's more, it could be prepared by the 1,2-dichloropropane.
The physical properties of this chemical are below: (1)ACD/LogP: 1.04; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1.04; (4)ACD/LogD (pH 7.4): 1.04; (5)ACD/BCF (pH 5.5): 3.61; (6)ACD/BCF (pH 7.4): 3.61; (7)ACD/KOC (pH 5.5): 87.32; (8)ACD/KOC (pH 7.4): 87.32; (9)#H bond acceptors: 1; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 1; (12)Polar Surface Area: 17.07; (13)Index of Refraction: 1.434; (14)Molar Refractivity: 25.63 cm3; (15)Molar Volume: 98.3 cm3; (16)Polarizability: 10.16 ×10-24 cm3; (17)Surface Tension: 30.3 dyne/cm; (18)Density: 1.291 g/cm3; (19)Flash Point: 41.8 °C; (20)Enthalpy of Vaporization: 34.88 kJ/mol; (21)Boiling Point: 110.1 °C at 760 mmHg; (22)Vapour Pressure: 24.1 mmHg at 25°C; (23)Exact Mass: 125.96392; (24)MonoIsotopic Mass: 125.96392; (25)Topological Polar Surface Area: 17.1; (26)Heavy Atom Count: 6; (27)Formal Charge: 0; (28)Complexity: 61.8.
When you are using this chemical, you should be very cautious. For being a kind of corrosive chemical, it may destroy living tissue on contact. Then it is flammable which may causes severe burns. Besides, it is irritating to respiratory system.
Therefore, you should be better take the following advices to protect yourself. Wear suitable protective clothing, gloves and eye/face protection. If in case of contact with eyes, rinse immediately with plenty of water and seek medical advice, and if in case of accident or if you feel unwell, seek medical advice immediately (show the label where possible). And you could keep away from sources of ignition - No smoking and then remember to avoid contacting with eyes.
Additionally, you could convert the following datas into the molecular structure:
(1)Canonical SMILES: CC(C(=O)Cl)Cl
(2)InChI: InChI=1S/C3H4Cl2O/c1-2(4)3(5)6/h2H,1H3
(3)InChIKey: JEQDSBVHLKBEIZ-UHFFFAOYSA-N
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