2-((4-methoxyphenyl)disulfanyl)benzo[d]thiazole

Reagent Code: #204131
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CAS Number 159357-91-2

science Other reagents with same CAS 159357-91-2

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Weight 305.445 g/mol
Formula C₁₄H₁₁NOS₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of sulfur-containing heterocyclic compounds, particularly in the development of pharmaceuticals with antimicrobial and antitumor activities. It serves as a disulfide coupling agent in organic synthesis, enabling the formation of symmetrical and unsymmetrical disulfide bridges in bioactive molecules. Its benzo[d]thiazole moiety contributes to enhanced binding affinity with biological targets, making it valuable in medicinal chemistry for designing enzyme inhibitors. Also applied in materials science for developing functional polymers with redox-active properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿11,400.00
inventory 5g
10-20 days ฿42,750.00

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2-((4-methoxyphenyl)disulfanyl)benzo[d]thiazole
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Used as a key intermediate in the synthesis of sulfur-containing heterocyclic compounds, particularly in the development of pharmaceuticals with antimicrobial and antitumor activities. It serves as a disulfide coupling agent in organic synthesis, enabling the formation of symmetrical and unsymmetrical disulfide bridges in bioactive molecules. Its benzo[d]thiazole moiety contributes to enhanced binding affinity with biological targets, making it valuable in medicinal chemistry for designing enzyme inhibit

Used as a key intermediate in the synthesis of sulfur-containing heterocyclic compounds, particularly in the development of pharmaceuticals with antimicrobial and antitumor activities. It serves as a disulfide coupling agent in organic synthesis, enabling the formation of symmetrical and unsymmetrical disulfide bridges in bioactive molecules. Its benzo[d]thiazole moiety contributes to enhanced binding affinity with biological targets, making it valuable in medicinal chemistry for designing enzyme inhibitors. Also applied in materials science for developing functional polymers with redox-active properties.

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