1-Hydroxyindan

99%

Reagent Code: #194826
fingerprint
CAS Number 6351-10-6

science Other reagents with same CAS 6351-10-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 134.18 g/mol
Formula C₉H₁₀O
badge Registry Numbers
MDL Number MFCD00003797
thermostat Physical Properties
Melting Point 52°C
Boiling Point 220 °C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Serves as a building block in the production of indane-based compounds, which are common in bioactive molecules and drug candidates. Also utilized in research for developing novel psychoactive substances and analogs, due to structural similarity to controlled compounds. Its hydroxyl group allows for derivatization in esterification and ether formation reactions. Employed in studies related to neurotransmitter analogs and central nervous system agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿360.00
inventory 25g
10-20 days ฿880.00
inventory 100g
10-20 days ฿3,230.00
inventory 500g
10-20 days ฿16,130.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-Hydroxyindan
No image available
Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Serves as a building block in the production of indane-based compounds, which are common in bioactive molecules and drug candidates. Also utilized in research for developing novel psychoactive substances and analogs, due to structural similarity to controlled compounds. Its hydroxyl group allows for derivatization in esterification and ether formation reactions. Employed in studies related to neurotransmitter analogs and ce
Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Serves as a building block in the production of indane-based compounds, which are common in bioactive molecules and drug candidates. Also utilized in research for developing novel psychoactive substances and analogs, due to structural similarity to controlled compounds. Its hydroxyl group allows for derivatization in esterification and ether formation reactions. Employed in studies related to neurotransmitter analogs and central nervous system agents.
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...