2,2′-Biphenyldimethanol

98%

Reagent Code: #149706
fingerprint
CAS Number 3594-90-9

science Other reagents with same CAS 3594-90-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.26 g/mol
Formula C₁₄H₁₄O₂
badge Registry Numbers
MDL Number MFCD00074889
thermostat Physical Properties
Melting Point 110-111 °C (lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of liquid crystal materials for display technologies. Its rigid biphenyl structure and hydroxyl functional groups make it ideal for polymerization reactions, especially in producing high-performance engineering plastics and polyesters with enhanced thermal stability. Also employed in chiral resolution processes due to its ability to form diastereomeric complexes. Additionally, serves as a building block in pharmaceuticals and agrochemicals where aromatic diols are required for molecular complexity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,480.00
inventory 5g
10-20 days ฿12,080.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2,2′-Biphenyldimethanol
No image available

Used as a key intermediate in the synthesis of liquid crystal materials for display technologies. Its rigid biphenyl structure and hydroxyl functional groups make it ideal for polymerization reactions, especially in producing high-performance engineering plastics and polyesters with enhanced thermal stability. Also employed in chiral resolution processes due to its ability to form diastereomeric complexes. Additionally, serves as a building block in pharmaceuticals and agrochemicals where aromatic diols

Used as a key intermediate in the synthesis of liquid crystal materials for display technologies. Its rigid biphenyl structure and hydroxyl functional groups make it ideal for polymerization reactions, especially in producing high-performance engineering plastics and polyesters with enhanced thermal stability. Also employed in chiral resolution processes due to its ability to form diastereomeric complexes. Additionally, serves as a building block in pharmaceuticals and agrochemicals where aromatic diols are required for molecular complexity.

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...