Chloroethyl chloroformate

Chloroethyl chloroformate
1-Chloroethyl chloroformate	2-Chloroethyl chloroformate
Names
	IUPAC names 1-Chloroethyl carbonochloridate; 2-Chloroethyl carbonochloridate
Identifiers
CAS Number	50893-53-3 (1-chloroethyl chloroformate) ; 627-11-2 (2-chloroethyl chloroformate) ;
3D model (JSmol)	Interactive image; Interactive image;
ChemSpider	454726 (1-chloroethyl chloroformate); 11802 (2-chloroethyl chloroformate);
PubChem CID	521305 (1-chloroethyl chloroformate); 12305 (2-chloroethyl chloroformate);
UNII	4D32H07Z9I ;
	InChI InChI=1S/C3H4Cl2O2/c1-2(4)7-3(5)6/h2H,1H3 Key: QOPVNWQGBQYBBP-UHFFFAOYSA-N; InChI=1/C3H4Cl2O2/c4-1-2-7-3(5)6/h1-2H2 Key: SVDDJQGVOFZBNX-UHFFFAOYAR;
	SMILES ClC(OC(Cl)C)=O; ClC(=O)OCCCl;
Properties
Chemical formula	C3H4Cl2O2
Molar mass	142.96 g·mol−1
Related compounds
Related chloroformates	Chloromethyl chloroformate
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Chloroethyl chloroformates (chemical formula: C₃H₄Cl₂O₂) are a pair of related chemical compounds. They can be used to form protecting groups and as N-dealkylating agents.^[1]

They are listed as extremely hazardous substances.^[2]

References[edit]

^ 'A new reagent for the selective, high-yield N-dealkylation of tertiary amines: improved syntheses of naltrexone and nalbuphine' R. A. Olofson, Jonathan T. Martz, Jean Pierre Senet, Marc Piteau, Thierry Malfroot J. Org. Chem., 1984, 49 (11), pp 2081–2082
^ Extremely Hazardous Chemicals

[1] 'A new reagent for the selective, high-yield N-dealkylation of tertiary amines: improved syntheses of naltrexone and nalbuphine' R. A. Olofson, Jonathan T. Martz, Jean Pierre Senet, Marc Piteau, Thierry Malfroot J. Org. Chem., 1984, 49 (11), pp 2081–2082

[2] Extremely Hazardous Chemicals

[1]

[2]