[(3-Methylthiophen-2-yl)methyl](triphenyl)phosphanium bromide

Base Information

• Chemical Name: [(3-Methylthiophen-2-yl)methyl](triphenyl)phosphanium bromide
• CAS No.: 78519-04-7
• Molecular Formula: C24H22PS.Br
• DSSTox Substance ID: DTXSID70604655

Synonyms:78519-04-7;SCHEMBL5861711;DTXSID70604655;GRUHMNYAAVMZIC-UHFFFAOYSA-M;[(3-Methylthiophen-2-yl)methyl](triphenyl)phosphanium bromide;(3-methyl-2-thenyl)triphenyl phosphonium bromide

Chemical Property of [(3-Methylthiophen-2-yl)methyl](triphenyl)phosphanium bromide

Chemical Property:

• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 452.03632
• Heavy Atom Count: 27
• Complexity: 372

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

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MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(SC=C1)C[P+](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4.[Br-]
• Use Description: Phosphonium, [(3-methyl-2-thienyl)methyl]triphenyl-, bromide is a chemical compound with potential applications across various fields. In the field of organic chemistry, it can serve as a versatile and reactive reagent for various chemical transformations, aiding researchers in the synthesis of complex organic molecules. Its unique structure, containing both a phosphonium cation and a thiophene moiety, makes it valuable in the development of novel materials and the creation of compounds with specific properties. Additionally, in academic research, Phosphonium, [(3-methyl-2-thienyl)methyl]triphenyl-, bromide may be employed as a reference material for studying reaction mechanisms and conducting studies in synthetic chemistry, contributing to advancements in the field. While specific uses may vary, its primary significance lies in organic synthesis and chemical research, making it a valuable tool for researchers and chemists exploring diverse applications in material science and organic chemistry.

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