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Chlorosarin
Names
	Preferred IUPAC name Propan-2-yl methylphosphonochloridate
	Other names O-Isopropyl methylphosphonochloridate; Isopropyl methylphosphonic chloride
Identifiers
CAS Number	1445-76-7 ;
3D model (JSmol)	Interactive image;
ChemSpider	92259 ;
PubChem CID	102124;
UNII	0DNX22ZOWK ;
CompTox Dashboard (EPA)	DTXSID40862669 ;
	InChI InChI=1S/C4H10ClO2P/c1-4(2)7-8(3,5)6/h4H,1-3H3 Key: RHAHLPAWJVKXAZ-UHFFFAOYSA-N ; InChI=1/C4H10ClO2P/c1-4(2)7-8(3,5)6/h4H,1-3H3 Key: RHAHLPAWJVKXAZ-UHFFFAOYAW;
	SMILES ClP(=O)(OC(C)C)C;
Properties
Chemical formula	C4H10ClO2P
Molar mass	156.55 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Chlorosarin is a chemical precursor used in the final step of one method for the production of the nerve agent sarin. Also known as O-isopropyl methylphosphonochloridate and isopropyl methylphosphonic chloride, it has a molecular weight of 156.55 g/mol and a molecular formula of C₄H₁₀Cl O₂P.

Safety

Chlorosarin will produce effects similar to those of sarin if it is absorbed into body, but they are less severe. However, like sarin, it is highly toxic and small doses of it would be lethal. The Chemical Weapons Convention also lists chlorosarin as well as other chemicals such chlorosoman and QL as controlled substances in Schedule 1.^[1]

Synthesis

Like GB, ClGB presents a varied preparation route. Overall, it is a lower cost chemical warfare agent than sarin. ClGB was one of the final intermediates of step five of the DMHP process, being known as a raw impurity and as a final precursor.^[2]

Chlorosarin can be synthesized from diisopropyl methylphosphonate (DIMP) and phosgene.

References

^ Chemical Weapons Convention. Annex on Chemicals. B. Schedules of Chemicals. Schedule 1 // Organisation for the Prohibition of Chemical Weapons
^ Sanches, M. L; Randolph, C. L; Barden, J. D; Bradley, S; Laughlin, L. L. Chemical Weapons Convention (CWC) Signatures Analysis. p 117