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  • 97674-02-7 TRIBUTYL(1-ETHOXYVINYL)TIN
Name:97674-02-7 TRIBUTYL(1-ETHOXYVINYL)TIN
CAS No:97674-02-7

PRODUCT DESCRIPTION

Product Name: TRIBUTYL(1-ETHOXYVINYL)TIN
Synonyms: (1-Ethoxyvinyl)tributyltin(IV);[1-(Tributylstannyl)vinyl]ethyl ether;1-Ethoxy-1-(tributylstannyl)ethene;1-Ethoxyethenyltributylstannane;Tributyl(1-ethoxyvinyl)stannane;Tributyl(1-ethoxyvinyl)tin(IV);Tributyl(1-ethoxyvinyl)tin,95%;ETHOXYVINYL TRIBUTYL TIN
CAS: 97674-02-7
MF: C16H34OSn
MW: 361.15
EINECS:
Product Categories: Organotin;Organotins;Organometallic Reagents;Stannanes
Mol File: 97674-02-7.mol
TRIBUTYL(1-ETHOXYVINYL)TIN Structure
TRIBUTYL(1-ETHOXYVINYL)TIN Chemical Properties
Melting point <0°C
Boiling point 85-86 °C0.1 mm Hg(lit.)
density 1.069 g/mL at 25 °C(lit.)
refractive index n20/D 1.476(lit.)
Fp >230 °F
storage temp. 2-8°C
form liquid
color colorless
Specific Gravity 1.069
Sensitive Moisture Sensitive
InChIKey HGXJOXHYPGNVNK-UHFFFAOYSA-N
Safety Information
Hazard Codes T,N
Risk Statements 21-25-36/38-48/23/25-50/53
Safety Statements 35-36/37/39-45-60-61
RIDADR UN 2788 6.1/PG 3
WGK Germany 3
TSCA No
HazardClass 6.1(b)
PackingGroup III
HS Code 29319090
MSDS Information
Provider Language
SigmaAldrich English
ACROS English
TRIBUTYL(1-ETHOXYVINYL)TIN Usage And Synthesis
Reaction Versatile tin reagent used for the introduction of a 1-ethoxyvinyl group via a Stille cross-coupling reaction, (palladium-catalyzed coupling of an organohalide (or pseudohalide) with an organotin compound). 
Chemical Properties Clear colorless liquid
Uses
Electrophilic methyl ketone equivalent used in a recent synthesis of a 13-oxophorbine (chlorophyll) from the corresponding 13-bromochlorin.
General Description
This vinylstannane undergoes Stille coupling with a vinyl triflate, giving, after hydrolysis, an α,β?unsaturated ketone, thus acting as an acetyl anion equivalent.
TRIBUTYL(1-ETHOXYVINYL)TIN Preparation Products And Raw materials
Preparation Products 1-(3-AMINO-PYRIDIN-2-YL)-ETHANONE-->1-QUINOLIN-3-YLETHANONE-->1-(1-BROMONAPHTHALEN-4-YL)ETHANONE-->2'-hydroxy-5'-(trifluoroMethyl)acetophenone-->3-IODOBENZYL ALCOHOL-->Benzonitrile, 4-acetyl-3-fluoro--->4-Methyl-3-nitroacetophenone-->5-ACETYL-2-METHOXYPYRIDINE, 97%

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