Gelest, Inc. TRI-n-BUTYLGERMANE, 99% GET8100

Description
Application Effects free-radical reductive addition of alkyl halides to olefins with AIBN.1,2 Reduces benzylic chlorides 70 X faster than silyl hydrides.3 Initiates radical cyclization of polyenes.4 Reference 1. Hershberger, J. Tetrahedron Lett. 1986, 26, 6289. 2. Pike, P. et al. Tetrahedron 1988, 44, 6295. 3. Mayr, H. et al. Angew. Chem., Int. Ed. Engl. 1992, 31, 1046. 4. Spino, C. et al. J. Org. Chem. 1999, 64, 5292. Safety Packaging Under Nitrogen Germanium-Base Reducing Agent Tri-n-butylgermane; Tributylgermanium hydride Reduces acid chlorides to aldehydes in presence of Pd(0) Effects free-radical reductive addition of alkyl halides to olefins Reduces benzylic chlorides 70x faster than silyl hydrides
Datasheet
Description
Application Effects free-radical reductive addition of alkyl halides to olefins with AIBN.1,2 Reduces benzylic chlorides 70 X faster than silyl hydrides.3 Initiates radical cyclization of polyenes.4 Reference 1. Hershberger, J. Tetrahedron Lett. 1986, 26, 6289. 2. Pike, P. et al. Tetrahedron 1988, 44, 6295. 3. Mayr, H. et al. Angew. Chem., Int. Ed. Engl. 1992, 31, 1046. 4. Spino, C. et al. J. Org. Chem. 1999, 64, 5292. Safety Packaging Under Nitrogen Germanium-Base Reducing Agent Tri-n-butylgermane; Tributylgermanium hydride Reduces acid chlorides to aldehydes in presence of Pd(0) Effects free-radical reductive addition of alkyl halides to olefins Reduces benzylic chlorides 70x faster than silyl hydrides
Datasheet

Suppliers

Company
Product
Description
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TRI-n-BUTYLGERMANE, 99% - GET8100 - Gelest, Inc.
Morrisville, PA, United States
TRI-n-BUTYLGERMANE, 99%
GET8100
TRI-n-BUTYLGERMANE, 99% GET8100
Application Effects free-radical reductive addition of alkyl halides to olefins with AIBN.1,2 Reduces benzylic chlorides 70 X faster than silyl hydrides.3 Initiates radical cyclization of polyenes.4 Reference 1. Hershberger, J. Tetrahedron Lett. 1986, 26, 6289. 2. Pike, P. et al. Tetrahedron 1988, 44, 6295. 3. Mayr, H. et al. Angew. Chem., Int. Ed. Engl. 1992, 31, 1046. 4. Spino, C. et al. J. Org. Chem. 1999, 64, 5292. Safety Packaging Under Nitrogen Germanium-Base Reducing Agent Tri-n-butylgermane; Tributylgermanium hydride Reduces acid chlorides to aldehydes in presence of Pd(0) Effects free-radical reductive addition of alkyl halides to olefins Reduces benzylic chlorides 70x faster than silyl hydrides

Application


Effects free-radical reductive addition of alkyl halides to olefins with AIBN.1,2 Reduces benzylic chlorides 70 X faster than silyl hydrides.3 Initiates radical cyclization of polyenes.4


Reference


1. Hershberger, J. Tetrahedron Lett. 1986, 26, 6289. 2. Pike, P. et al. Tetrahedron 1988, 44, 6295. 3. Mayr, H. et al. Angew. Chem., Int. Ed. Engl. 1992, 31, 1046. 4. Spino, C. et al. J. Org. Chem. 1999, 64, 5292.


Safety


  • Packaging Under Nitrogen
    Germanium-Base Reducing Agent
    Tri-n-butylgermane; Tributylgermanium hydride
  • Reduces acid chlorides to aldehydes in presence of Pd(0)
  • Effects free-radical reductive addition of alkyl halides to olefins
  • Reduces benzylic chlorides 70x faster than silyl hydrides
Supplier's Site Datasheet

Technical Specifications

  Gelest, Inc.
Product Category Inorganic Chemicals and Compounds
Product Number GET8100
Product Name TRI-n-BUTYLGERMANE, 99%
Type OrganoMetallics
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