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1-TRIMETHYLSILOXY-1,3-BUTADIENE

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1-TRIMETHYLSILOXY-1,3-BUTADIENE Basic information

Product Name:
1-TRIMETHYLSILOXY-1,3-BUTADIENE
Synonyms:
  • Silane, (1,3-butadienyloxy)trimethyl-
  • 1-TRIMETHYLSILYLOXY-1,3-BUTADIENE
  • 1-TRIMETHYLSILOXY-1,3-BUTADIENE
  • 1-(TRIMETHYLSILYLOXY)-1,3-BUTADIENE, 98% , MIXTURE OF ISOMERS
  • 1-(Trimethylsilyloxy)-1,3-butadiene, mixture of isomers, 98%
  • (1,3-Butadienyloxy)trimethylsilane
  • 1,3-Butadienyl(trimethylsilyl) ether
  • 4-(Trimethylsiloxy)-1,3-butadiene
CAS:
6651-43-0
MF:
C7H14OSi
MW:
142.27
Product Categories:
  • Enol Ethers
  • Organic Building Blocks
  • Oxygen Compounds
  • Building Blocks
  • Chemical Synthesis
  • Enol Ethers
  • Organic Building Blocks
  • Oxygen Compounds
Mol File:
6651-43-0.mol
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1-TRIMETHYLSILOXY-1,3-BUTADIENE Chemical Properties

Boiling point:
131 °C(lit.)
Density 
0.811 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.448(lit.)
Flash point:
77 °F
storage temp. 
2-8°C
solubility 
Sol most standard organic solvents.
Specific Gravity
0.811
Hydrolytic Sensitivity
7: reacts slowly with moisture/water
BRN 
1902024
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Safety Information

Hazard Codes 
Xi
Risk Statements 
10-36/37/38
Safety Statements 
26-36/37/39
RIDADR 
UN 1993 3/PG 3
WGK Germany 
3
10-21
TSCA 
No
HazardClass 
3.2
PackingGroup 
III

MSDS

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1-TRIMETHYLSILOXY-1,3-BUTADIENE Usage And Synthesis

Chemical Properties

clear light yellow liquid

Physical properties

bp 131 °C, bp 49.5 °C/25 mmHg; d 0.811 g cm?3.

Uses

1-Trimethylsilyloxy-1,3-butadiene is an easily prepared reactive diene for Diels–Alder reactions and other cycloadditions; reactive silyl enol ether for aldol and Michael reactions, and electrophilic additions.

Uses

1-(Trimethylsiloxy)-1,3-butadiene is commonly employed as diene in the Diels-Alder reaction.

Uses

1-Trimethylsiloxy-1,3-butadiene is a diene used in the Diels-Alder reaction.

General Description

Mechanism of Diels-Alder reaction between 1-(trimethylsiloxy)-1,3-butadiene and 4,6-dinitrobenzofuroxan has been studied using state-of-the-art computational methods.

Purification Methods

Purify it by fractional distillation and collect the fractions with the required 1H NMR. Store it under N2 — it is a flammable and moisture-sensitive liquid. [Caseau et al. Bull Soc Chim Fr 16658 1972, Belge Patent 670,769, Chem Abstr 65 5487d 1966.]

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