1-Bromo-4-(isopropylsulfinyl)benzene

≥95%

Reagent Code: #40036
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CAS Number 1129287-54-2

science Other reagents with same CAS 1129287-54-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.15 g/mol
Formula C₉H₁₁BrOS
badge Registry Numbers
MDL Number MFCD20529459
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. It is particularly valuable in the development of sulfoxide-containing molecules, which exhibit significant biological activity. Additionally, it is employed in asymmetric synthesis due to its chiral sulfinyl group, enabling the creation of enantiomerically pure compounds. Its reactivity also makes it suitable for use in cross-coupling reactions, contributing to the construction of complex organic frameworks.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿9,459.00
inventory 1g
10-20 days ฿2,952.00
inventory 100mg
10-20 days ฿792.00
inventory 250mg
10-20 days ฿1,188.00

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1-Bromo-4-(isopropylsulfinyl)benzene
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. It is particularly valuable in the development of sulfoxide-containing molecules, which exhibit significant biological activity. Additionally, it is employed in asymmetric synthesis due to its chiral sulfinyl group, enabling the creation of enantiomerically pure compounds. Its reactivity also makes it suitable for use in cross-coupling reactions, contributing to

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. It is particularly valuable in the development of sulfoxide-containing molecules, which exhibit significant biological activity. Additionally, it is employed in asymmetric synthesis due to its chiral sulfinyl group, enabling the creation of enantiomerically pure compounds. Its reactivity also makes it suitable for use in cross-coupling reactions, contributing to the construction of complex organic frameworks.

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