Atomfair N,1-Bis(5-(trimethylstannyl)thiophen-2-yl)methanimine C15H23NS2Sn2

Description N,1-Bis(5-(trimethylstannyl)thiophen-2-yl)methanimine (CAS No. 2704541-57-9) is a high-purity organotin compound with the molecular formula C15H23NS2Sn2, designed for advanced research and synthesis applications. This compound features a unique (E)-N,1-bis(5-trimethylstannylthiophen-2-yl)methanimine structure, integrating stannyl and thiophene moieties for versatile reactivity in cross-coupling reactions, polymer chemistry, and materials science. Ideal for use in controlled environments, it is supplied with detailed analytical data (NMR, HPLC, MS) to ensure consistency and traceability. Store under inert conditions to maintain stability. For researchers exploring organometallic catalysts, conductive polymers, or optoelectronic materials, this reagent offers exceptional precision and performance.

Description

N,1-Bis(5-(trimethylstannyl)thiophen-2-yl)methanimine (CAS No. 2704541-57-9) is a high-purity organotin compound with the molecular formula C₁₅H₂₃NS₂Sn₂, designed for advanced research and synthesis applications. This compound features a unique (E)-N,1-bis(5-trimethylstannylthiophen-2-yl)methanimine structure, integrating stannyl and thiophene moieties for versatile reactivity in cross-coupling reactions, polymer chemistry, and materials science. Ideal for use in controlled environments, it is supplied with detailed analytical data (NMR, HPLC, MS) to ensure consistency and traceability. Store under inert conditions to maintain stability. For researchers exploring organometallic catalysts, conductive polymers, or optoelectronic materials, this reagent offers exceptional precision and performance.

CAS No: 2704541-57-9
Molecular Formula: C15H23NS2Sn2
Molecular Weight: 518.9
Exact Mass: 518.93100
Monoisotopic Mass: 520.93160
IUPAC Name: (E)-N,1-bis(5-trimethylstannylthiophen-2-yl)methanimine
SMILES: C[Sn](C)(C)C1=CC=C(S1)/C=N/C2=CC=C(S2)[Sn](C)(C)C
Synonyms: N,1-Bis(5-(trimethylstannyl)thiophen-2-yl)methanimine, 2704541-57-9

Application

This compound serves as a key intermediate in the synthesis of conjugated polymers and organometallic complexes, particularly in the development of organic semiconductors and photovoltaic materials. Its dual stannyl-thiophene structure enables efficient Stille coupling reactions, facilitating the construction of ??-extended systems for electronic devices. Researchers also utilize it in the preparation of tin-functionalized ligands for catalysis and sensor applications.

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