Stannane, tributyl(2-ethoxyethenyl)-

Base Information

• Chemical Name: Stannane, tributyl(2-ethoxyethenyl)-
• CAS No.: 64724-29-4
• Molecular Formula: C16H34 O Sn
• Molecular Weight: 361.155
• Hs Code.: 2931900090
• European Community (EC) Number: 677-907-9
• Mol file: 64724-29-4.mol

Synonyms:20420-43-3;Stannane, tributyl(2-ethoxyethenyl)-;64724-29-4;(Z)-tributyl(2-ethoxyvinyl)stannane;z-(1)-Ethoxy-(2)-(tributylstannyl)ethylen;SCHEMBL18114;CS-0106663;D78548;EN300-194399;TRIBUTYL[(1E)-2-ETHOXYETHENYL]STANNANE

Chemical Property of Stannane, tributyl(2-ethoxyethenyl)-

Chemical Property:

• Vapor Pressure: 0.000127mmHg at 25°C
• Melting Point: 84-87℃
• Refractive Index: n20/D1.479
• Boiling Point: 345°C at 760 mmHg
• Flash Point: 162.4°C
• PSA: 9.23000
• Density: 1.082
• LogP: 5.92490
• Storage Temp.: 2-8°C
• Water Solubility.: Soluble in water.
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 12
• Exact Mass: 362.163168
• Heavy Atom Count: 18
• Complexity: 180

Purity/Quality:

98%,99%, ^*data from raw suppliers

cis-1-Ethoxy-2-(tributylstannyl)ethene ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T,N
• Hazard Codes: T,N
• Statements: 21-25-36/38-48/23/25-50/53
• Safety Statements: 35-36/37/39-45-60-61

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCC[Sn](CCCC)(CCCC)C=COCC
• Isomeric SMILES: CCCC[Sn](CCCC)(CCCC)/C=C/OCC
• Uses: cis-1-Ethoxy-2-(tri-n-butylstannyl)ethylene is widely used in pharmaceutical research and as reagent.

Technology Process of Stannane, tributyl(2-ethoxyethenyl)-

There total 7 articles about Stannane, tributyl(2-ethoxyethenyl)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 93.0%

tri-n-butyl-tin hydride (688-73-3) + 1-ethoxyacetylene (927-80-0) → tributyl(2-ethoxyvinyl)stannane (20420-43-3,64724-29-4,124582-30-5)

Guidance literature:

1 h;; distn.;;

Reference yield:

tri-n-butyl-tin hydride (688-73-3) + 1-ethoxyacetylene (927-80-0) → (E)-2-ethoxyvinyltributyltin (20420-43-3,64724-29-4,124582-30-5)

Guidance literature:

Reference yield:

→ (E)-2-ethoxyvinyltributyltin (20420-43-3,64724-29-4,124582-30-5)

Guidance literature:

upstream raw materials:

tri-n-butyl-tin hydride

1-ethoxyacetylene

(Z)-1-bromo-2-ethoxyethene

tributyltin chloride

Downstream raw materials:

(E)-3-ethoxy-1-phenylprop-2-ene-1-one

(Z)-2-(2-ethoxyethenyl)acetanilide

trans,trans-2,4-Hexadienal

(E)-3-phenylpropenal

Refernces

• 1、 -. "HETEROCYCLIC COMPOUNDS". Page/Page column 30; 31. . Retrieved 2009/08/18.
• 2、 -. "NOVEL AZACYCLY-SUBSTITUTED ARYLTHIENOPYRIMIDINONES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS MEDICAMENTS". Page/Page column 104-105. . Retrieved 2008/06/13.