ALLYLTRIPHENYLTIN

Product Information

Molecular Formula:
C21H20Sn
Molecular Weight:
391.09
Description
Allyltriphenylstannane can be used:• As a reagent in the C-H phenylation of azoles catalyzed by palladium.• As an allylating reagent in the alkylidene Meldrum's acids allylation catalyzed by Sc(OTf)3.• As a reagent in the total synthesis of an antifungal molecule (+)-ambruticin S.
Synonyms
TINALLYLTRIPHENYL; TRIPHENYLALLYLTIN; allyltriphenyl-stannan; allyltriphenylstannane; dowco187; ent50909; triphenyl-2-propenyl-stannan; ALLYLTRIPHENYLTIN
IUPAC Name
triphenyl(prop-2-enyl)stannane
Canonical SMILES
C=CC[Sn](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3
InChI
InChI=1S/3C6H5.C3H5.Sn/c3*1-2-4-6-5-3-11-3-2/h3*1-5H3H,1-2H2
InChI Key
NDUYAGLANMHJHF-UHFFFAOYSA-N
Boiling Point
421.4°C at 760 mmHg
Melting Point
71-74°C(lit.)
Flash Point
Not applicable
Purity
>95.0%(W)
Density
1,07 g/cm3

Safety Information

Hazards
H301 + H311 + H331 - H410
Precautionary Statement
P273 - P280 - P301 + P310 + P330 - P302 + P352 + P312 - P304 + P340 + P311

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
5
Exact Mass
392.058703 g/mol
Monoisotopic Mass
392.058703 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
22
Formal Charge
0
Complexity
284
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
JP-2021095474-A Perfluoropolyether-modified polysilazane and its manufacturing method, surface treatment agent, cured film and article 2019-12-16
JP-2021020984-A Method for Producing Perfluorooxyalkylene Group-Containing Polymer Having Reactive Cyril Group 2019-07-25
CN-113474167-A Substrate with conductive layer and touch panel 2019-04-02
JP-6773258-B1 Base material with conductive layer and touch panel 2019-04-02
JP-WO2020203447-A1 Base material with conductive layer and touch panel 2019-04-02
TW-202105419-A Base material and touch panel with conductive layer 2019-04-02
WO-2020203447-A1 Substrate with electrically conductive layers, and touch panel 2019-04-02
WO-2020054484-A1 Modified multi-component copolymer, rubber composition, resin composition, tire and resin product 2018-09-14
EP-3851489-A1 Modified multi-component copolymer, rubber composition, resin composition, tire and resin product 2018-09-14
JP-WO2020054484-A1 Modified multipolymers, rubber compositions, resin compositions, tires and resin products 2018-09-14

Literatures

PMID Publication Date Title Journal
2004 1976-02-01 Electrocardiographic changes and cardiac arrhythmias in patients receiving psychotropic drugs The American journal of cardiology
1176 1975-12-01 Circadian variations of hormonal content in the nervous system of the crayfish Comparative biochemistry and physiology. A, Comparative physiology
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Related Products

Online Inquiry
  • Verification code
USA
  • International:
  • US & Canada (Toll free):
  • Email:
  • Fax:
UK
  • Email:
Copyright © 2024 BOC Sciences. All rights reserved.
Top
Inquiry Basket