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2-Chloro-1,3,2-dioxaphospholane

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2-Chloro-1,3,2-dioxaphospholane Basic information

Product Name:
2-Chloro-1,3,2-dioxaphospholane
Synonyms:
  • 1,3,2-Dioxaphospholane, 2-chloro-
  • 1,3,2-Dioxaphosphorane.2-chloro-
  • 2-dioxaphospholane,2-chloro-3
  • Ethylenephosphorochloridite
  • AURORA KA-1222
  • ETHYLENE CYCL-CHLOROPHOSPHITE
  • ETHYLENE CYCLO-CHLOROPHOSPHITE
  • ETHYLENE CHLOROPHOSPHITE
CAS:
822-39-9
MF:
C2H4ClO2P
MW:
126.48
EINECS:
212-499-4
Product Categories:
  • Biochemistry
  • Nucleosides, Nucleotides & Related Reagents
  • Phosphorylating and Phosphorothioating Agents
  • Phosphorylation
  • Protecting Agents, Phosphorylating Agents & Condensing Agents
  • Synthetic Organic Chemistry
  • Phosphorylating and Phosphitylating Agents
Mol File:
822-39-9.mol
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2-Chloro-1,3,2-dioxaphospholane Chemical Properties

Melting point:
-28°C(lit.)
Boiling point:
62 °C/20 mmHg (lit.)
Density 
1.422 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.489(lit.)
Flash point:
158 °F
storage temp. 
2-8°C
solubility 
Chloroform (Slightly)
form 
clear liquid
color 
Colorless to Light yellow
Sensitive 
Moisture Sensitive
BRN 
506179
Stability:
Extremely Moisture Sensitive
CAS DataBase Reference
822-39-9(CAS DataBase Reference)
NIST Chemistry Reference
Ethylene chlorophosphite(822-39-9)
EPA Substance Registry System
1,3,2-Dioxaphospholane, 2-chloro- (822-39-9)
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Safety Information

Hazard Codes 
C
Risk Statements 
14-34-37
Safety Statements 
26-36/37/39-45-8-25
RIDADR 
UN 3264 8/PG 2
WGK Germany 
3
1-10
Hazard Note 
Highly reactive cyclic phosphitylating reagent which
TSCA 
Yes
HS Code 
2934.99.9001
HazardClass 
8
PackingGroup 
II

MSDS

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2-Chloro-1,3,2-dioxaphospholane Usage And Synthesis

Chemical Properties

Clear Colourless Oil

Uses

Highly reactive cyclic phosphitylating reagent which provides fast coupling rates, and hydrolytic cleavage occurs more readily than with acyclic analogs

Uses

Ethylene chlorophosphite acts as a phosphitylating agent involved in the preparation of phosphocholine and spirophosphoranes. For example, it is used in the phosphorylation of p-tert-butyl(thia)calixarenes.

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