Basic information Safety Supplier Related

2-Chloromethoxyethylchloride

Basic information Safety Supplier Related

2-Chloromethoxyethylchloride Basic information

Product Name:
2-Chloromethoxyethylchloride
Synonyms:
  • chloroethylchloromethylether
  • 2-CHLOROMETHOXYETHYLCHLORIDE
  • 2-CHLOROETHYL CHLOROMETHYL ETHER
  • 1-CHLORO-2-CHLOROMETHOXYETHANE
  • (2-Chloroethoxy)methyl Chloride
  • 2-CHLOROETHYLCHLOROMETHYLESTER
  • 2-CHLOROETHYL CHLOROMETHYL ETHER 96+%
  • 2-Chloroethyl Chloromethyl Ether >
CAS:
1462-33-5
MF:
C3H6Cl2O
MW:
128.99
Mol File:
1462-33-5.mol
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2-Chloromethoxyethylchloride Chemical Properties

Boiling point:
147 °C
Density 
1,28 g/cm3
refractive index 
1.4570-1.4600
storage temp. 
Keep in dark place,Inert atmosphere,2-8°C
solubility 
Chloroform
form 
Oil
color 
Yellow
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Safety Information

Risk Statements 
10-23/24/25-34
Safety Statements 
16-26-36-45
RIDADR 
2929
HS Code 
2909.19.1800
HazardClass 
6.1/3
PackingGroup 
II
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2-Chloromethoxyethylchloride Usage And Synthesis

Chemical Properties

Yellow Oil. 2-Chloromethoxyethylchloride is soluble in most commonly used organic solvents, including ethereal (THF, diethyl ether), halogenated (CH2Cl2, CHCl3, CCl4), and hydrocarbon solvents; incompatible with alcohol solvents.

Uses

(2-Chloroethoxy)methyl Chloride (cas# 1462-33-5) is a compound useful in organic synthesis.

Synthesis

The most conveniently prepared of 2-Chloromethoxyethylchloride is by reaction of 2-chloroethanol and 1,3,5-trioxane with HCl(g) at 0 °C (1.0 mol scale, 66% yield).

Precautions

2-Chloromethoxyethylchloride is a deviate of Chloromethyl ethers, which are recognized carcinogens. The reagent should be prepared and handled in an efficient fume hood, and skin contact should be avoided. Chloromethyl ethers are also moisture-sensitive and should be stored and transferred under an inert atmosphere. Excess reagent should be hydrolyzed in water before removing it from the fume hood.

References

1. Ogle, C. A.; Wilson, T. E.; Stowe, J. A. S 1990, 495.
2. Hutchison, A. J.; Kishi, Y. JACS 1979, 101, 6786.
3. Farren, J. W.; Fife, H. F.; Clark, F. E.; Garland, C. E. JACS 1925, 47, 2419.
4. For similar procedures, see ref 5 and Holy, A.; Rosenberg, I.; Dvorakova, H. CCC 1989, 54, 2190 (4.6 mol scale, 74% yield)

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