3-Thiazol-2-yl-benzaldehyde

≥95%

Reagent Code: #241646
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CAS Number 885465-97-4

science Other reagents with same CAS 885465-97-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.23 g/mol
Formula C₁₀H₇NOS
badge Registry Numbers
MDL Number MFCD06797781
thermostat Physical Properties
Boiling Point 355.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antithrombotic and anticoagulant agents. It serves as a building block in heterocyclic chemistry, enabling the construction of complex molecules with biological activity. Commonly employed in the preparation of thiazole-containing Schiff bases, which exhibit antimicrobial and anti-inflammatory properties. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance molecular stability and reactivity. Its conjugated structure makes it suitable for use in organic electronics and fluorescent probes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,260.00
inventory 5g
10-20 days ฿25,200.00
inventory 10g
10-20 days ฿50,200.00
3-Thiazol-2-yl-benzaldehyde
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antithrombotic and anticoagulant agents. It serves as a building block in heterocyclic chemistry, enabling the construction of complex molecules with biological activity. Commonly employed in the preparation of thiazole-containing Schiff bases, which exhibit antimicrobial and anti-inflammatory properties. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its a

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antithrombotic and anticoagulant agents. It serves as a building block in heterocyclic chemistry, enabling the construction of complex molecules with biological activity. Commonly employed in the preparation of thiazole-containing Schiff bases, which exhibit antimicrobial and anti-inflammatory properties. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance molecular stability and reactivity. Its conjugated structure makes it suitable for use in organic electronics and fluorescent probes.

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