trans-1,2-Cyclohexanediol

98%

Reagent Code: #158353
label
Alias Trans-1,2-cyclohexanediol; trans-1,2-cyclohexanediol, cyclohexanediol
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CAS Number 1460-57-7

science Other reagents with same CAS 1460-57-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 116.16 g/mol
Formula C₆H₁₂O₂
badge Registry Numbers
EC Number 215-956-6
MDL Number MFCD00063611
thermostat Physical Properties
Melting Point 101-104 °C(lit.)
Boiling Point 117 °C (12.7517 mmHg)
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a chiral building block in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its rigid cyclohexane backbone and two adjacent hydroxyl groups make it valuable for designing ligands in asymmetric catalysis. Also employed in the development of polymers and resins where stereochemistry influences material properties. Due to its ability to form cyclic derivatives, it is utilized in the synthesis of protective groups and molecular recognition systems.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿310.00
5g
10-20 days ฿660.00
25g
10-20 days ฿1,150.00
100g
10-20 days ฿3,520.00
500g
10-20 days ฿13,860.00
2.5kg
10-20 days ฿34,650.00
trans-1,2-Cyclohexanediol
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Used as a chiral building block in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its rigid cyclohexane backbone and two adjacent hydroxyl groups make it valuable for designing ligands in asymmetric catalysis. Also employed in the development of polymers and resins where stereochemistry influences material properties. Due to its ability to form cyclic derivatives, it is utilized in the synthesis of protective groups and molecular recognition systems.

Used as a chiral building block in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its rigid cyclohexane backbone and two adjacent hydroxyl groups make it valuable for designing ligands in asymmetric catalysis. Also employed in the development of polymers and resins where stereochemistry influences material properties. Due to its ability to form cyclic derivatives, it is utilized in the synthesis of protective groups and molecular recognition systems.

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