2-Ethynyl-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione

98%

Reagent Code: #184992
fingerprint
CAS Number 1310384-76-9

science Other reagents with same CAS 1310384-76-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.95 g/mol
Formula C₇H₈BNO₄
badge Registry Numbers
MDL Number MFCD11215242
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a specialized boron-containing reagent in organic synthesis, particularly in cyclization and heterocycle formation reactions. Its strained ring structure and alkyne functionality enable participation in transition metal-catalyzed coupling reactions, such as Sonogashira and Diels-Alder reactions, facilitating the construction of complex polycyclic frameworks. Commonly employed in the development of pharmaceutical intermediates and functional materials where precise boron placement is required. Its unique scaffold also shows potential in medicinal chemistry for designing enzyme inhibitors due to its ability to mimic transition states in metabolic pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,630.00
inventory 250mg
10-20 days ฿4,270.00
inventory 1g
10-20 days ฿12,000.00
inventory 5g
10-20 days ฿50,400.00
2-Ethynyl-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione
No image available

Used as a specialized boron-containing reagent in organic synthesis, particularly in cyclization and heterocycle formation reactions. Its strained ring structure and alkyne functionality enable participation in transition metal-catalyzed coupling reactions, such as Sonogashira and Diels-Alder reactions, facilitating the construction of complex polycyclic frameworks. Commonly employed in the development of pharmaceutical intermediates and functional materials where precise boron placement is required. Its

Used as a specialized boron-containing reagent in organic synthesis, particularly in cyclization and heterocycle formation reactions. Its strained ring structure and alkyne functionality enable participation in transition metal-catalyzed coupling reactions, such as Sonogashira and Diels-Alder reactions, facilitating the construction of complex polycyclic frameworks. Commonly employed in the development of pharmaceutical intermediates and functional materials where precise boron placement is required. Its unique scaffold also shows potential in medicinal chemistry for designing enzyme inhibitors due to its ability to mimic transition states in metabolic pathways.

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...