Product Name

  • Name

    2-Chloropropionyl chloride

  • EINECS 231-540-7
  • CAS No. 7623-09-8
  • Article Data40
  • CAS DataBase
  • Density 1.291 g/cm3
  • Solubility MAY DECOMPOSE
  • Melting Point -71 °C
  • Formula C3H4Cl2O
  • Boiling Point 110.1 °C at 760 mmHg
  • Molecular Weight 126.97
  • Flash Point 41.8 °C
  • Transport Information UN 2920 8/PG 2
  • Appearance clear colorless to light yellow liquid
  • Safety 26-36/37/39-45-25-16
  • Risk Codes 10-35-37
  • Molecular Structure Molecular Structure of 7623-09-8 (2-Chloropropionyl chloride)
  • Hazard Symbols CorrosiveC
  • Synonyms 2-Chloropropionyl chloride
  • PSA 17.07000
  • LogP 1.37910

Synthetic route

(R,S)-2-chloropropionic acid
598-78-7

(R,S)-2-chloropropionic acid

2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

Conditions
ConditionsYield
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
849585-22-4

LACTIC ACID

2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

Conditions
ConditionsYield
With pyridine; thionyl chloride
With phosphorus pentachloride; water
propionyl chloride
79-03-8

propionyl chloride

2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

Conditions
ConditionsYield
With iodine; chlorine
With sulfuryl dichloride; iodine
propionyl chloride
79-03-8

propionyl chloride

A

2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

B

2-chloropropionyl chloride
625-36-5

2-chloropropionyl chloride

Conditions
ConditionsYield
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
76-00-6

1,1,1-trichloropropan-2-ol

A

2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

B

1,1,2-trichloropropene
21400-25-9

1,1,2-trichloropropene

C

1,1,1-trichloroisopropyl α-chloropropionate
78049-86-2

1,1,1-trichloroisopropyl α-chloropropionate

Conditions
ConditionsYield
With phosphorus pentoxide Heating; Yield given. Yields of byproduct given;
With phosphorus pentoxide Product distribution; Heating;
With phosphorus pentoxide Heating; Yield given;
sulfuryl dichloride
7791-25-5

sulfuryl dichloride

iodine
7553-56-2

iodine

propionyl chloride
79-03-8

propionyl chloride

2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

N,N'-diisopropyl selenourea
13120-10-0

N,N'-diisopropyl selenourea

3-isopropyl-2-isopropylimino-5-methyl-1,3-selenazolidin-4-one

3-isopropyl-2-isopropylimino-5-methyl-1,3-selenazolidin-4-one

Conditions
ConditionsYield
With pyridine In tetrahydrofuran at 0℃;100%
2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

N,0-dimethylhydroxylamine
1117-97-1

N,0-dimethylhydroxylamine

2-chloro-N-methoxy-N-methylpropionamide

2-chloro-N-methoxy-N-methylpropionamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃;100%
3,4-dihydro-2(1H)-quinolone
553-03-7

3,4-dihydro-2(1H)-quinolone

2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

6-(2-chloropropanoyl)-3,4-dihydroquinolin-2(1H)-one
62618-75-1

6-(2-chloropropanoyl)-3,4-dihydroquinolin-2(1H)-one

Conditions
ConditionsYield
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 CS227.7 g (91%)
2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

L-Phenylalaninol
3182-95-4

L-Phenylalaninol

C15H19Cl2NO3
1048970-96-2

C15H19Cl2NO3

Conditions
ConditionsYield
In dichloromethane at 20℃; for 16h;100%
2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

1-t-Butoxycarbonylpiperazine
57260-71-6

1-t-Butoxycarbonylpiperazine

tert-butyl 4-(2-chloropropanoyl)piperazine-1-carboxylate
1181803-80-4

tert-butyl 4-(2-chloropropanoyl)piperazine-1-carboxylate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃; for 1h;100%
2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

3-amino-4-[(methylsulfonyl)methyl]-N-(5-phenyl-1,3,4-thiadiazol-2-yl)benzamide

3-amino-4-[(methylsulfonyl)methyl]-N-(5-phenyl-1,3,4-thiadiazol-2-yl)benzamide

3-[(2-chloropropanoyl)amino]-4-[(methylsulfonyl)methyl]-N-(5-phenyl-1,3,4-thiadiazol-2-yl)benzamide

3-[(2-chloropropanoyl)amino]-4-[(methylsulfonyl)methyl]-N-(5-phenyl-1,3,4-thiadiazol-2-yl)benzamide

Conditions
ConditionsYield
In toluene at 100℃; for 2h;100%
2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

2-benzylamino-2-methyl-1-propanol
10250-27-8

2-benzylamino-2-methyl-1-propanol

N-benzyl-2-chloro-N-(1-hydroxy-2-methylpropan-2-yl)propanamide

N-benzyl-2-chloro-N-(1-hydroxy-2-methylpropan-2-yl)propanamide

Conditions
ConditionsYield
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
7623-09-8

2-chloropropionyl chloride

(2S)-2-(benzyl-amino)butane-1,4-diol

(2S)-2-(benzyl-amino)butane-1,4-diol

N-benzyl-2-chloro-N-[(2S)-1,4-dihydroxybutan-2-yl]propanamide

N-benzyl-2-chloro-N-[(2S)-1,4-dihydroxybutan-2-yl]propanamide

Conditions
ConditionsYield
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
7623-09-8

2-chloropropionyl chloride

(2R)-2-(benzylamino)butane-1,4-diol
117554-09-3

(2R)-2-(benzylamino)butane-1,4-diol

N-benzyl-2-chloro-N-[(2R)-1,4-dihydroxybutan-2-yl]propanamide

N-benzyl-2-chloro-N-[(2R)-1,4-dihydroxybutan-2-yl]propanamide

Conditions
ConditionsYield
With triethylamine In isopropyl alcohol at 0℃; for 0.166667h;100%
2-amino-4-chloro-benzoic acid methyl ester
5900-58-3

2-amino-4-chloro-benzoic acid methyl ester

2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

(rac)-methyl 4-chloro-2-(2-chloropropanamido)benzoate

(rac)-methyl 4-chloro-2-(2-chloropropanamido)benzoate

Conditions
ConditionsYield
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%
2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

aniline
62-53-3

aniline

2-chloro-N-phenylpropanamide
21262-52-2

2-chloro-N-phenylpropanamide

Conditions
ConditionsYield
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
7623-09-8

2-chloropropionyl chloride

p-toluidine
106-49-0

p-toluidine

2-chloro-N-(4-methyl-phenyl)propionamide
40781-30-4, 51063-63-9, 147372-41-6

2-chloro-N-(4-methyl-phenyl)propionamide

Conditions
ConditionsYield
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
7623-09-8

2-chloropropionyl chloride

4-chloro-aniline
106-47-8

4-chloro-aniline

2-chloro-N-(4-chloro-phenyl)propionamide
40781-33-7, 51063-58-2, 21262-05-5

2-chloro-N-(4-chloro-phenyl)propionamide

Conditions
ConditionsYield
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
7623-09-8

2-chloropropionyl chloride

4-bromo-aniline
106-40-1

4-bromo-aniline

N-(4-bromophenyl)-2-chloropropanamide
21262-08-8

N-(4-bromophenyl)-2-chloropropanamide

Conditions
ConditionsYield
In toluene at 120℃; for 1h;99%
In toluene Heating;
With pyridine In chloroform at 20℃; for 12h;
2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

3,4-difluoroaniline
3863-11-4

3,4-difluoroaniline

2-chloro-N-(3,4-difluoro-phenyl)-propionamide
868771-20-4

2-chloro-N-(3,4-difluoro-phenyl)-propionamide

Conditions
ConditionsYield
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
313369-40-3

tert-butyl 6-amino-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indole-2-carboxylate

2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

tert-butyl 6-[(3-chloropropanoyl)amino]-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indole-2-carboxylate
313369-41-4

tert-butyl 6-[(3-chloropropanoyl)amino]-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indole-2-carboxylate

Conditions
ConditionsYield
With sodium hydrogencarbonate; dmap In benzene99%
3,4-dihydro-3-oxo-2H-1,4-benzoxazine
5466-88-6

3,4-dihydro-3-oxo-2H-1,4-benzoxazine

2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

6-(2-chloropropanoyl)-2H-1,4-benzoxazin-3(4H)-one
293741-63-6

6-(2-chloropropanoyl)-2H-1,4-benzoxazin-3(4H)-one

Conditions
ConditionsYield
With aluminum (III) chloride In 1,2-dichloro-ethane at 20℃; for 12h;99%
2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

2-(benzylamino)-2-methyl-propan-1,3-diol
91340-32-8

2-(benzylamino)-2-methyl-propan-1,3-diol

N-benzyl-2-chloro-N-(1,3-dihydroxy-2-methylpropan-2-yl)propanamide

N-benzyl-2-chloro-N-(1,3-dihydroxy-2-methylpropan-2-yl)propanamide

Conditions
ConditionsYield
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
7623-09-8

2-chloropropionyl chloride

3-[3-amino-4-(trifluoromethoxy)phenyl]-7-bromoquinazolin-4(3H)-one

3-[3-amino-4-(trifluoromethoxy)phenyl]-7-bromoquinazolin-4(3H)-one

N-[5-(7-bromo-4-oxoquinazolin-3(4H)-yl)-2-(trifluoromethoxy)phenyl]-2-chloropropanamide

N-[5-(7-bromo-4-oxoquinazolin-3(4H)-yl)-2-(trifluoromethoxy)phenyl]-2-chloropropanamide

Conditions
ConditionsYield
In toluene at 100℃; for 2h;99%
In toluene at 100℃; for 2h;99%
4-nitro-phenol
100-02-7

4-nitro-phenol

2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

4-nitrophenyl 2-chloropropanoate
141479-87-0

4-nitrophenyl 2-chloropropanoate

Conditions
ConditionsYield
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
7623-09-8

2-chloropropionyl chloride

4-fluoroaniline
371-40-4

4-fluoroaniline

N-4'-fluorophenyl-2-chloropropanamide
21262-04-4

N-4'-fluorophenyl-2-chloropropanamide

Conditions
ConditionsYield
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
7623-09-8

2-chloropropionyl chloride

3-amino-2-imino-3,4-dihydro-2H-1,3-benzothiazin-4-one
57675-96-4

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
122604-30-2

2-(1-Chloroethyl)-1,2,4-triazolo<5,1-b><1,3>benzothiazin-9-one

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 2h; Heating;98%
2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

triethylamine
121-44-8

triethylamine

N-triethyl-N-(2-propanoyl-N-triethylammonium chloride) ammonium chloride

N-triethyl-N-(2-propanoyl-N-triethylammonium chloride) ammonium chloride

Conditions
ConditionsYield
In benzene for 1h; Heating;98%
2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

4-methoxy-aniline
104-94-9

4-methoxy-aniline

2-chloro-N-(4-methoxy-phenyl)propionamide
40781-31-5, 51063-61-7, 21262-10-2

2-chloro-N-(4-methoxy-phenyl)propionamide

Conditions
ConditionsYield
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%
C22H20BrClN2O3
930786-49-5

C22H20BrClN2O3

2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

C25H23BrCl2N2O4

C25H23BrCl2N2O4

Conditions
ConditionsYield
In 1,4-dioxane at 20℃; for 1h;98%
1,3-dihydro-2H-benzimidazol-2-one
615-16-7

1,3-dihydro-2H-benzimidazol-2-one

2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

5-(2-chloropropanoyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one

5-(2-chloropropanoyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one

Conditions
ConditionsYield
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
40033-95-2

Spiro-<2,3-dihydro-4H-1,3-benzoxazine-1,2'-cyclohexan>-4-one

2-chloropropionyl chloride
7623-09-8

2-chloropropionyl chloride

3-(2-chloro-1-oxopropyl)spiro[2H-1,3-benzoxazine-2,1'-cyclohexan]-4(3H)-one

3-(2-chloro-1-oxopropyl)spiro[2H-1,3-benzoxazine-2,1'-cyclohexan]-4(3H)-one

Conditions
ConditionsYield
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;

2-Chloropropionyl chloride Specification

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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