33304-76-6

Usage

Uses

Used in Organic Synthesis:
3-(triphenylstannanyl)propan-1-ol is used as a reagent for the preparation of various organotin compounds, which are important in the development of new materials and chemical processes.
Used in Pharmaceutical and Agrochemical Industries:
3-(triphenylstannanyl)propan-1-ol is utilized as a precursor in the synthesis of pharmaceuticals and agrochemicals, contributing to the creation of novel drugs and pesticides.
Used in Medicinal Chemistry:
3-(triphenylstannanyl)propan-1-ol is being studied for its potential role in medicinal chemistry, where it may contribute to the discovery of new therapeutic agents.
Used in Coordination Chemistry:
3-(triphenylstannanyl)propan-1-ol is also being explored as a ligand in coordination chemistry, which could lead to the development of new catalysts and materials with unique properties.

Upstream product

• 892-20-6 triphenylstannane 
• 107-18-6 allyl alcohol 
• 639-58-7 triphenyltin chloride 

Downstream Products

• 881192-37-6 (3-methoxypropyl)triphenylstannane 
• 648930-61-4 triphenyl[3-(4-biphenyloxy)propyl]tin 
• 35843-43-7 (3-chloropropyl)triphenylstannane 
• 799278-89-0 3-(triphenylstannyl)propyl 4-methylbenzenesulfonate 
• 144889-65-6 (3-hydroxypropyl)iododiphenyltin 
• 35843-44-8 (C₆H₅)3SnCH₂CH₂CH₂Br 
• 35843-50-6 (C₆H₅)2ClSn(CH₂)3Cl 

Relevant academic research and scientific papers

Evaluation of functionalized mesoporous silica SBA-15 as a carrier system for Ph3Sn(CH2)3OH against the A2780 ovarian carcinoma cell line

SBA-15|Sn3, a mesoporous silica-based material (derivative of SBA-15) loaded with an organotin compound Ph3Sn(CH2)3OH (Sn3), possesses improved antitumor potential against the A2780 high-grade serous ovarian carcinoma cell

Synthesis and Characterization of Readily Modified Poly(aryl)(alkoxy)stannanes by use of Hypercoordinated Sn Monomers

The synthesis and solid-state molecular structures of two dichlorido(aryl)(alkyl) tin compounds, 5 and 8, both key intermediates to tunable polystannane architectures, are reported. The materials were further investigated by single-crystal XRD and a DFT a

Proof of Concept Studies Directed Towards Designed Molecular Wires: Property-Driven Synthesis of Air and Moisture-Stable Polystannanes

Polystannanes with azobenzene moieties designed to protect the Sn–Sn backbone from light- and moisture-induced degradation are described. The azo-stannyl precursor 3 (70 %) is converted in good yields (88–91 %) to the mono- (4), and dichlorostannanes (5),

Synthesis of a tin-functionalized cyclopentadiene derivative

A 3-tert-butyl-1-(stannylpropyl)-functionalized cyclopentadienyl ligand precursor 6 is readily available in 64% overall yield from allylic alcohol 1 by a three-step reaction sequence including Pd-catalyzed hydrostannylation with Ph3SnH. Treatment with FeCl2 and ZrCl4 · 2THF afforded corresponding ferrocene and zirconocene derivatives. Transmetallation of Sn-Ph with Li-Bu was observed under these reaction conditions by using BuLi as a base.

Sulphur-substituted Organotin Compounds. Part 8. Preparation and Reactions of 3-(p-Tolylthio)propyl- and 4-(p-Tolylthio)butyl-triphenyltin. Interactions with Tetracyanoethylene

The reactions of SnPh3 (n= 3 or 4) with mercury(II) chloride, bromine and iodine lead to phenyl-tin bond cleavage.In contrast, reactions with methyl iodide provide SnPh3 and MeSC6H4Me-p.Charge-transfer adducts are formed between SnPh3 (n= 1-4) and tetracyanoethylene or p-bromoanil.The values of λmax. of the complexes indicate similar donor character for SnPh3 (n= 2,3, or 4); however, the compound SnPh3(CH2SC6H4Me-p) is a stronger donor.