33304-76-6

Basic information

• Product Name: 3-(triphenylstannanyl)propan-1-ol
• CAS NO: 33304-76-6
• Molecular Formula: C₂₁H₂₂OSn
• Molecular Weight: 409.1088
• Mol File: 33304-76-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 474.4°C at 760 mmHg
• Flash Point: 240.7°C
• Vapor Pressure: 8.29E-10mmHg at 25°C
• CAS DataBase Reference: 3-(triphenylstannanyl)propan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(triphenylstannanyl)propan-1-ol(33304-76-6)
• EPA Substance Registry System: 3-(triphenylstannanyl)propan-1-ol(33304-76-6)

Safety Data

• Hazardous Substances Data: 33304-76-6(Hazardous Substances Data)

Usage

General Description

3-(triphenylstannanyl)propan-1-ol is a chemical compound with the molecular formula C21H22OSn. It is an organotin compound that contains a triphenylstannyl group and a propanol group. 3-(triphenylstannanyl)propan-1-ol is primarily used as a reagent in organic synthesis, particularly in the preparation of various organotin compounds and as a precursor in the synthesis of pharmaceuticals and agrochemicals. It is known to have some toxic properties and should be handled with caution. Additionally, 3-(triphenylstannanyl)propan-1-ol is also being studied for its potential role in medicinal chemistry and as a ligand in coordination chemistry.

Upstream product

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

Downstream Products

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

Relevant articles and documents

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

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),

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.