()-B-Chlorodiisopinocampheylborane

60% in Heptane,ca. 1.7mol/L

Reagent Code: #70079
label
Alias (+)Diisopine pinocampyl chloride borane ;(+)-B-Diisopine pinocampyl chloride borane
fingerprint
CAS Number 112246-73-8

science Other reagents with same CAS 112246-73-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 320.75 g/mol
Formula C₂₀H₃₄BCl
badge Registry Numbers
MDL Number MFCD00074808
thermostat Physical Properties
Melting Point 53-55 °C(lit.)
inventory_2 Storage & Handling
Density 0.91
Storage 2~8°C

description Product Description

Used as a chiral reagent in organic synthesis, particularly for asymmetric hydroboration of alkenes to produce optically active alcohols after oxidation. It is highly effective in asymmetric synthesis, offering excellent stereocontrol in the formation of chiral centers. Commonly applied in the pharmaceutical industry for the production of enantiomerically pure compounds, which are crucial for drug development. Its selectivity and efficiency make it a valuable tool in the synthesis of complex molecules with specific stereochemical requirements.

format_list_bulleted Product Specification

Test Parameter Specification
Concentration 58.5-62
Specific Gravity (20/4°C) 0.868-0.872
Solution 47-54
Appearance Colorless liquid

Available Sizes & Pricing

Size Availability Unit Price Quantity
1L
10-20 days ฿15,000.00
25ml
10-20 days ฿740.00
100ml
10-20 days ฿2,400.00
500ml
10-20 days ฿8,580.00
()-B-Chlorodiisopinocampheylborane
No image available
Used as a chiral reagent in organic synthesis, particularly for asymmetric hydroboration of alkenes to produce optically active alcohols after oxidation. It is highly effective in asymmetric synthesis, offering excellent stereocontrol in the formation of chiral centers. Commonly applied in the pharmaceutical industry for the production of enantiomerically pure compounds, which are crucial for drug development. Its selectivity and efficiency make it a valuable tool in the synthesis of complex molecules with
Used as a chiral reagent in organic synthesis, particularly for asymmetric hydroboration of alkenes to produce optically active alcohols after oxidation. It is highly effective in asymmetric synthesis, offering excellent stereocontrol in the formation of chiral centers. Commonly applied in the pharmaceutical industry for the production of enantiomerically pure compounds, which are crucial for drug development. Its selectivity and efficiency make it a valuable tool in the synthesis of complex molecules with specific stereochemical requirements.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...