4-(2-CHLOROACETYL)MORPHOLINE
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
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)
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
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
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