Benzo[d]thiazol-5-ylmethanol

98%

Reagent Code: #148501
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CAS Number 394223-37-1

science Other reagents with same CAS 394223-37-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.21 g/mol
Formula C₈H₇NOS
badge Registry Numbers
MDL Number MFCD12408380
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity. Its structure serves as a building block in heterocyclic chemistry, enabling the creation of more complex molecules with potential antifungal, antibacterial, or anti-inflammatory properties. Also employed in the preparation of fluorescent dyes and sensors due to the inherent photophysical properties of the benzothiazole core. Its hydroxyl group allows for further functionalization, making it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,150.00
inventory 250mg
10-20 days ฿10,440.00
inventory 1g
10-20 days ฿30,550.00
inventory 5g
10-20 days ฿86,620.00

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Benzo[d]thiazol-5-ylmethanol
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity. Its structure serves as a building block in heterocyclic chemistry, enabling the creation of more complex molecules with potential antifungal, antibacterial, or anti-inflammatory properties. Also employed in the preparation of fluorescent dyes and sensors due to the inherent photophysical properties of the benzothiazole core. Its hydroxyl group allows for f

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity. Its structure serves as a building block in heterocyclic chemistry, enabling the creation of more complex molecules with potential antifungal, antibacterial, or anti-inflammatory properties. Also employed in the preparation of fluorescent dyes and sensors due to the inherent photophysical properties of the benzothiazole core. Its hydroxyl group allows for further functionalization, making it valuable in medicinal chemistry for structure-activity relationship studies.

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