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Diisopropylzinc
Identifiers
CAS Number	625-81-0 ;
3D model (JSmol)	Interactive image;
ChemSpider	11347073 ;
ECHA InfoCard	100.221.415
PubChem CID	5207587;
CompTox Dashboard (EPA)	DTXSID10409984 ;
	InChI InChI=1S/2C3H7.Zn/c21-3-2;/h23H,1-2H3; Key: KDUNMLRPPVCIGP-UHFFFAOYSA-N ; InChI=1/2C3H7.Zn/c21-3-2;/h23H,1-2H3;/rC6H14Zn/c1-5(2)7-6(3)4/h5-6H,1-4H3 Key: KDUNMLRPPVCIGP-LSPCJBSIAV;
	SMILES CC(C)[Zn]C(C)C;
Properties
Chemical formula	C6H14Zn
Molar mass	151.56 g/mol
	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

Diisopropylzinc is an organozinc compound with the chemical formula ZnC₆H₁₄.^[1]

It is the key reagent in the Soai reaction, which is both autocatalytic and enantiospecific.^[2] This chemical is pyrophoric, bursting into flame in air or in contact with water. It is generally packaged in toluene. ^[3]

References

^ Benjamin Bederson; Herbert Walther (2002). Advances in Atomic, Molecular, and Optical Physics. Gulf Professional Publishing. pp. 250–. ISBN 978-0-12-003848-0. Retrieved 2013-08-06.
^ Shibata, Takanori; Morioka, Hiroshi; Hayase, Tadakatsu; Choji, Kaori; Soai, Kenso (1996). "Highly Enantioselective Catalytic Asymmetric Automultiplication of Chiral Pyrimidyl Alcohol". Journal of the American Chemical Society. 118 (2): 471–472. doi:10.1021/ja953066g.
^ "Diisopropylzinc 1.0M toluene 625-81-0". MilliporeSigma. Retrieved 8 January 2022.

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[BedersonWalther2002-1] Benjamin Bederson; Herbert Walther (2002). Advances in Atomic, Molecular, and Optical Physics. Gulf Professional Publishing. pp. 250–. ISBN 978-0-12-003848-0. Retrieved 2013-08-06.

[2] Shibata, Takanori; Morioka, Hiroshi; Hayase, Tadakatsu; Choji, Kaori; Soai, Kenso (1996). "Highly Enantioselective Catalytic Asymmetric Automultiplication of Chiral Pyrimidyl Alcohol". Journal of the American Chemical Society. 118 (2): 471–472. doi:10.1021/ja953066g.

[3] "Diisopropylzinc 1.0M toluene 625-81-0". MilliporeSigma. Retrieved 8 January 2022.

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