(4'-Bromo-[1,1'-biphenyl]-4-yl)(methyl)sulfane

≥95%

Reagent Code: #130054
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CAS Number 3393-00-8

science Other reagents with same CAS 3393-00-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.2 g/mol
Formula C₁₃H₁₁BrS
badge Registry Numbers
MDL Number MFCD06201356
thermostat Physical Properties
Melting Point 144.0-146.4 °C
Boiling Point 371.6±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.44±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure, featuring a stable biphenyl core, a reactive bromo group, and a methylsulfanyl substituent, allows for cross-coupling reactions and additional functionalization, making it valuable in the development of complex aromatic compounds. Commonly employed in Suzuki and Ullmann-type reactions to build biaryl frameworks. Also utilized in the synthesis of functional materials, including liquid crystals and organic semiconductors, due to its versatile substituents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,840.00
inventory 250mg
10-20 days ฿16,730.00

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(4'-Bromo-[1,1'-biphenyl]-4-yl)(methyl)sulfane
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure, featuring a stable biphenyl core, a reactive bromo group, and a methylsulfanyl substituent, allows for cross-coupling reactions and additional functionalization, making it valuable in the development of complex aromatic compounds. Commonly employed in Suzuki and Ullmann-type reactions to build biaryl frameworks. Also utilized in the synthesis of functional materials, includin

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure, featuring a stable biphenyl core, a reactive bromo group, and a methylsulfanyl substituent, allows for cross-coupling reactions and additional functionalization, making it valuable in the development of complex aromatic compounds. Commonly employed in Suzuki and Ullmann-type reactions to build biaryl frameworks. Also utilized in the synthesis of functional materials, including liquid crystals and organic semiconductors, due to its versatile substituents.

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