Lithium trisiamylborohydride

0.6 M solution in THF, MkSeal

Reagent Code: #202009
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CAS Number 60217-34-7

science Other reagents with same CAS 60217-34-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.18 g/mol
Formula LiB[CH(CH₃)CH(CH₃)₂]₃H
badge Registry Numbers
MDL Number MFCD00011700
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a selective reducing agent in organic synthesis, particularly for the reduction of esters to alcohols in the presence of more sensitive functional groups. It exhibits high chemoselectivity, making it valuable in complex molecule synthesis where control over reactivity is crucial. Commonly employed in pharmaceutical and fine chemical industries for multi-step syntheses requiring mild and precise reduction conditions. Its bulky structure contributes to steric control, enabling selective transformations in sterically hindered environments.

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Size Availability Unit Price Quantity
inventory 50ml
10-20 days ฿6,280.00
Lithium trisiamylborohydride
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Used as a selective reducing agent in organic synthesis, particularly for the reduction of esters to alcohols in the presence of more sensitive functional groups. It exhibits high chemoselectivity, making it valuable in complex molecule synthesis where control over reactivity is crucial. Commonly employed in pharmaceutical and fine chemical industries for multi-step syntheses requiring mild and precise reduction conditions. Its bulky structure contributes to steric control, enabling selective transformat

Used as a selective reducing agent in organic synthesis, particularly for the reduction of esters to alcohols in the presence of more sensitive functional groups. It exhibits high chemoselectivity, making it valuable in complex molecule synthesis where control over reactivity is crucial. Commonly employed in pharmaceutical and fine chemical industries for multi-step syntheses requiring mild and precise reduction conditions. Its bulky structure contributes to steric control, enabling selective transformations in sterically hindered environments.

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