Basic information Safety Supplier Related

4-(2-CHLOROACETYL)MORPHOLINE

Basic information Safety Supplier Related

4-(2-CHLOROACETYL)MORPHOLINE Basic information

Product Name:
4-(2-CHLOROACETYL)MORPHOLINE
Synonyms:
  • 2-Chloro-1-(morpholin-4-yl)ethan-1-one
  • 4-(2-Chloroacetyl)morpholine 98%
  • 2-Chloro-1-morpholinoethan-1-one, 95+%
  • 2-CHLORO-1-MORPHOLIN-4-YL-ETHANONE >98%
  • 4-(CHLOROACETYL)MORPHOLINE, 97+%
  • 2-Chloro-1-(4-morpholinyl)ethanone, 2-Chloro-1-morpholinoethanone, 2-Morpholino-2-oxoethyl chloride, 4-Morpholinylcarbonylmethyl chloride, N-(Chloroacetyl)morpholine, Chloroacetic acid morpholide, Chloroacetic acid morpholine amide, Morpholine chloroacetamide
  • 1-Morpholino-2-chloroethanone
  • 2-Chloro-1-(4-Morpholinyl)ehanone
CAS:
1440-61-5
MF:
C6H10ClNO2
MW:
163.6
EINECS:
215-880-3
Product Categories:
  • ACETYLHALIDE
  • Heterocycles
  • MTS & Sulfhydryl Active Reagents
Mol File:
1440-61-5.mol
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4-(2-CHLOROACETYL)MORPHOLINE Chemical Properties

Melting point:
26-30 °C
Boiling point:
152-160 °C(Press: 6 Torr)
Density 
1.257 g/mL at 25 °C
refractive index 
n20/D 1.512
Flash point:
110 °C
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
pka
-1.26±0.20(Predicted)
form 
Solid
color 
Colourless to Pale Yellow Oil
Stability:
Hygroscopic
CAS DataBase Reference
1440-61-5(CAS DataBase Reference)
EPA Substance Registry System
Morpholine, 4-(chloroacetyl)- (1440-61-5)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-22
Safety Statements 
26-36/37/39
RIDADR 
UN3261
WGK Germany 
3
Hazard Note 
Irritant
HazardClass 
8
PackingGroup 
III
HS Code 
29349990

MSDS

  • Language:English Provider:ALFA
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4-(2-CHLOROACETYL)MORPHOLINE Usage And Synthesis

Chemical Properties

Colorless liquid

Uses

The chloroacetyl derivatives are microbicides for adhesives, cellulose foams, oil emulsions, cooling water, etc.

Synthesis

110-91-8

79-04-9

1440-61-5

Step 1: Morpholine (1.00 mL, 11.5 mmol) and toluene (30 mL) were added to a dry three-necked flask equipped with a magnetic stirrer under nitrogen protection. Potassium carbonate (3.17 g, 22.9 mmol) was then added and stirred until completely dissolved. Chloroacetyl chloride (0.91 mL, 11.4 mmol) was slowly added dropwise under the cooling of an ice bath, and after completion of the dropwise addition, the ice bath was removed, the temperature was raised to 60 °C and the reaction was continuously stirred for 2 hours. After completion of the reaction, the reaction mixture was cooled to room temperature, filtered to remove insoluble solids, and the solids were washed with a small amount of toluene. The filtrate and washings were combined and concentrated under reduced pressure to remove the solvent to give N-chloroacetylmorpholine as a white solid (1.87 g, quantitative yield). The product was characterized by 1H-NMR (270 MHz, CDCl3): δ 3.51-3.54 (m, 2H), 3.62-3.65 (m, 2H), 3.68-3.74 (m, 4H), 4.07 (s, 2H).

References

[1] Patent: EP1650194, 2006, A1. Location in patent: Page/Page column 34
[2] Patent: WO2012/72019, 2012, A1. Location in patent: Page/Page column 71-72
[3] Molecules, 2015, vol. 20, # 11, p. 19984 - 20013
[4] Patent: WO2016/147144, 2016, A1. Location in patent: Page/Page column 222
[5] Journal of Medicinal Chemistry, 2009, vol. 52, # 21, p. 6660 - 6671

4-(2-CHLOROACETYL)MORPHOLINESupplier

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