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1 References  














Diisopropylzinc






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From Wikipedia, the free encyclopedia
 


Diisopropylzinc
Skeletal formula of diisopropylzinc
Ball-and-stick model of the diisopropylzinc molecule
Identifiers

CAS Number

3D model (JSmol)

ChemSpider
ECHA InfoCard 100.221.415 Edit this at Wikidata

PubChem CID

CompTox Dashboard (EPA)

  • InChI=1S/2C3H7.Zn/c2*1-3-2;/h2*3H,1-2H3; checkY

    Key: KDUNMLRPPVCIGP-UHFFFAOYSA-N checkY

  • InChI=1/2C3H7.Zn/c2*1-3-2;/h2*3H,1-2H3;/rC6H14Zn/c1-5(2)7-6(3)4/h5-6H,1-4H3

    Key: KDUNMLRPPVCIGP-LSPCJBSIAV

  • 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).

checkY verify (what is checkY☒N ?)

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[edit]

  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.
  • ^ 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.
  • t
  • e

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Diisopropylzinc&oldid=1066465341"

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    This page was last edited on 18 January 2022, at 13:56 (UTC).

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