8-Chloro-1-n-octanol

≥99%(GC)

Reagent Code: #156492
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CAS Number 23144-52-7

science Other reagents with same CAS 23144-52-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.67 g/mol
Formula C₈H₁₇ClO
badge Registry Numbers
MDL Number MFCD00040005
thermostat Physical Properties
Boiling Point 129-130 °C/11mm Hg (lit.)
inventory_2 Storage & Handling
Density 0.976 g/mL at 25 °C (lit.)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain central nervous system agents and local anesthetics. Its structure allows for further functionalization, making it valuable in creating active pharmaceutical ingredients. Also utilized in research settings for developing novel organic compounds with potential biological activity. The presence of both chlorine and hydroxyl groups enables selective reactions useful in multi-step synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5ml
10-20 days ฿1,570.00
inventory 25ml
10-20 days ฿5,530.00
inventory 100ml
10-20 days ฿15,900.00
8-Chloro-1-n-octanol
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain central nervous system agents and local anesthetics. Its structure allows for further functionalization, making it valuable in creating active pharmaceutical ingredients. Also utilized in research settings for developing novel organic compounds with potential biological activity. The presence of both chlorine and hydroxyl groups enables selective reactions useful in multi-step synthesis.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain central nervous system agents and local anesthetics. Its structure allows for further functionalization, making it valuable in creating active pharmaceutical ingredients. Also utilized in research settings for developing novel organic compounds with potential biological activity. The presence of both chlorine and hydroxyl groups enables selective reactions useful in multi-step synthesis.

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