(4-Benzyloxyphenyl)tributylstannane

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Products Intro: Product Name:(4-Benzyloxyphenyl)tributylstannane
CAS:145745-05-7
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Products Intro: Product Name:(4-Benzyloxyphenyl)tributylstannane
CAS:145745-05-7
Purity:(4-Benzyloxyphenyl)tributylstannane Package:1G Remarks:721131-1G
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Products Intro: Product Name:(4-Benzyloxyphenyl)tributylstannane
CAS:145745-05-7
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Products Intro: Product Name:Tributyl[4-(phenylmethoxy)phenyl]stannane
CAS:145745-05-7
Purity:>=95% Remarks:481694
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Products Intro: Product Name:(4-Benzyloxyphenyl)tributylstannane
CAS:145745-05-7
(4-Benzyloxyphenyl)tributylstannane Basic information
Product Name:(4-Benzyloxyphenyl)tributylstannane
Synonyms:(4-Benzyloxyphenyl)tributylstannane;[4-(Benzyloxy)phenyl]tributylstannane, Benzyl 4-(tributylstannyl)phenyl ether;1-(Benzyloxy)-4-(tributylstannyl)benzene;[4-(Benzyloxy)phenyl]tributyltin;tributyl-(4-phenylmethoxyphenyl)stannane;Stannane, tributyl[4-(phenylmethoxy)phenyl]-;SKL191
CAS:145745-05-7
MF:C25H38OSn
MW:473.28
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Mol File:145745-05-7.mol
(4-Benzyloxyphenyl)tributylstannane Structure
(4-Benzyloxyphenyl)tributylstannane Chemical Properties
Boiling point 489.3±47.0 °C(Predicted)
density 1.128 g/cm3 at 25 °C
refractive index n20/D1.546
Fp >110℃
form liquid
InChI1S/C13H11O.3C4H9.Sn/c1-3-7-12(8-4-1)11-14-13-9-5-2-6-10-13;3*1-3-4-2;/h1,3-10H,11H2;3*1,3-4H2,2H3;
InChIKeyDRDMDSYSKAAPQQ-UHFFFAOYSA-N
SMILESCCCC[Sn](CCCC)(CCCC)c1ccc(OCc2ccccc2)cc1
Safety Information
Hazard Codes T,N
Risk Statements 21-25-36/38-48/23/25-50/53
Safety Statements 36/37/39-45-60-61
RIDADR UN 2788 6.1 / PGIII
WGK Germany 3
HS Code 2931200000
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 3 Oral
Acute Tox. 4 Dermal
Aquatic Acute 1
Aquatic Chronic 1
Eye Irrit. 2
Repr. 1B
Skin Irrit. 2
STOT RE 1 Inhalation
MSDS Information
(4-Benzyloxyphenyl)tributylstannane Usage And Synthesis
UsesReactant for:
  • Preparation of epoxy-substituted aryl alkenes by Stille coupling reactions with allylic carbonates
  • Preparation of polycyclic meroterpenoids based on Stille couplings and titanocene catalysis
(4-Benzyloxyphenyl)tributylstannane Preparation Products And Raw materials
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