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Lithium triisobutylhydroborate

CAS NO.38721-52-7

  • Min.Order: 1 Metric Ton
  • Payment Terms: L/C,D/A,D/P,T/T,Other
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Product Details

Keywords

  • Lithium triisobutylhydroborate
  • 38721-52-7
  • C12H28BLi

Quick Details

  • ProName: Lithium triisobutylhydroborate
  • CasNo: 38721-52-7
  • Molecular Formula: C12H28BLi
  • Appearance: clear colorless solution
  • Application: 38721-52-7
  • DeliveryTime: Within 3-7days
  • PackAge: As requested
  • Port: China Main Port
  • ProductionCapacity: 300 Metric Ton/Day
  • Purity: 98%
  • Storage: keep in dry and ventilated
  • Transportation: By air or by sea
  • LimitNum: 1 Metric Ton

Superiority

Lithium triisobutylhydroborate Basic information
Product Name: Lithium triisobutylhydroborate
Synonyms: LITHIUM TRI-S-BUTYLHYDROBORATE;LITHIUM TRI-SEC-BUTYLBOROHYDRIDE;LITHIUM TRI-SEC-BUTYLHYDRIDOBORATE;LITHIUM TRIISOBUTYLHYDROBORATE;L-SELECTRIDE(R);lithium,(beta-4)-borate(1-hydrotris(1-methylpropyl)-;lithiumtri-sec-butylborohydride,calselect li,;lithiumtri-sec-butylborohydride,calselect li,intetrahydrofuran
CAS: 38721-52-7
MF: C12H28BLi
MW: 190.1
EINECS: 254-101-1
Product Categories: B (Classes of Boron Compounds);Classes of Metal Compounds;Li (Lithium) Compounds;Reduction;Synthetic Organic Chemistry;Tetrahydroborates;Typical Metal Compounds
Mol File: 38721-52-7.mol
Lithium triisobutylhydroborate Structure
 
Lithium triisobutylhydroborate Chemical Properties
density  0.89 g/mL at 25 °C
Fp  1 °F
storage temp.  Flammables area
Water Solubility  reacts
Sensitive  Moisture Sensitive
BRN  4007327
CAS DataBase Reference 38721-52-7(CAS DataBase Reference)
 
Safety Information
Hazard Codes  F,C
Risk Statements  11-14/15-17-34-35-19-40-37
Safety Statements  16-26-36/37/39-43-45-7/8-30
RIDADR  UN 3394 4.2/PG 1
WGK Germany  1
10
HazardClass  4.3
PackingGroup  II
 
Lithium triisobutylhydroborate Usage And Synthesis
Chemical Properties clear colourless solution
Usage Reducing agent. Reagent for: Enantioselective synthesis of a-amino acids via reduction of N-tert-butanesulfinyl ketimine esters. Diastereoselective reduction reactions. Hydride reduction of the Danishefsky pyranones. Asymmetric reductive aldol reaction of enones with a-alkoxy aldehydes. Synthesis of alkanols by carbonylation reactions.

 

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