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54125-02-9

54125-02-9 Structure

54125-02-9 Structure
IdentificationMore
[Name]

1-METHOXY-3-TRIMETHYLSILOXY-1,3-BUTADIENE
[CAS]

54125-02-9
[Synonyms]

1-METHOXY-3-TRIMETHYLSILOXY-1,3-BUTADIENE
1-METHOXY-3-(TRIMETHYLSILOXY)BUTADIENE
1-METHOXY-3-TRIMETHYLSILYLOXY-1,3-BUTADIENE
DANISHEFSKY'S DIENE
TRANS-1-METHOXY-3-TRIMETHYLSILOXY-1,3-BUTADIENE
TRANS-1-METHOXY-3-(TRIMETHYLSILYLOXY)-1,3-BUTADIENE
TRANS-1-METHOXY-3-TRIMETHYLSILOXY-&
1-Methoxy-3-(trimethylsiloxy)butadiene(Danishefsky`sDiene)
Silane, (2E)-3-methoxy-1-methylene-2-propenyloxytrimethyl-
Danishefsky-Kitahara diene.
1-METHOXY-3-TRIMETHYLSILOXY-1,3-BUTADIENE, 98+%
(1E)-3-(Trimethylsilyloxy)-1-methoxy-1,3-butadiene
(E)-1-Methoxy-3-(trimethylsiloxy)-1,3-butadiene
(E)-1-Methoxy-3-[(trimethylsilyl)oxy]-1,3-butadiene
[[(E)-3-Methoxy-1-methylene-2-propenyl]oxy]trimethylsilane
Methyl[(1E)-3-(trimethylsiloxy)-1,3-butadienyl] ether
[EINECS(EC#)]

629-035-5
[Molecular Formula]

C8H16O2Si
[MDL Number]

MFCD00008498
[Molecular Weight]

172.3
[MOL File]

54125-02-9.mol
Chemical PropertiesBack Directory
[Boiling point ]

68-69 °C/14 mmHg (lit.)
[density ]

0.885 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.454(lit.)
[Fp ]

113 °F
[storage temp. ]

2-8°C
[form ]

liquid
[Specific Gravity]

0.89
[Water Solubility ]

Miscible with most organic solvents. Immiscible with water.
[Hydrolytic Sensitivity]

8: reacts rapidly with moisture, water, protic solvents
[Sensitive ]

Moisture Sensitive
[Merck ]

14,6001
[BRN ]

1616761
[CAS DataBase Reference]

54125-02-9(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)
GHS02
[Signal word ]

Warning
[Hazard statements ]

H226
[Precautionary statements ]

P210-P233-P240-P241-P242-P243
[Risk Statements ]

R10:Flammable.
[Safety Statements ]

S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
S24/25:Avoid contact with skin and eyes .
[RIDADR ]

UN 1993 3/PG 3
[WGK Germany ]

3
[F ]

10-21
[TSCA ]

No
[HazardClass ]

3
[PackingGroup ]

III
[HS Code ]

2931900090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Diethyl ether-->Sodium-->Triethylamine-->Benzene-->Acetonitrile-->Sodium acetate-->Zinc chloride-->Sodium iodide-->Chlorotrimethylsilane-->Lithium bromide-->Acetylacetaldehyde dimethyl acetal-->4-Methoxy-3-buten-2-one-->Trimethylsilyl trifluoromethanesulfonate
[Preparation Products]

5-Hydroxybenzo[b]furan-->2H-Pyran-4(3H)-one-->4-Methoxy-3-buten-2-one-->4H-Pyran-4-one, 2,3-dihydro-2-[(phenylmethoxy)methyl]-
Hazard InformationBack Directory
[Uses]

1-Methoxy-3-trimethylsiloxy-1,3-butadiene is employed as a reagent in Mannich-Michael reaction for the synthesis of piperidinones and enaminones. As Diels-Alder diene, it is used in the synthesis of pyridones and pyranones, sulfone analogues of griseofulvin (sulfogriseofulvins) and 4H-1-aminopyrroles and 4, 5H-pyrazoles.
[General Description]

trans-1-methoxy-3-trimethylsiloxy-1,3-butadiene is a funtionalized Diels-Alder diene. Mukaiyama-Michael-type addition/heterocyclization of trans-1-methoxy-3-trimethylsiloxy-1,3-butadiene (Danishefsky′s diene) with 1,2-diaza-1,3-butadiene has been investigated. Asymmetric hetero-Diels-Alder cyclization of Danishefsky′s diene with benzaldehyde catalyzed by mesoporous inorganic/metalorganic hybrid materials has been reported.
[Purification Methods]

It may contain up to 1% of the precursor 4-methoxybut-4-ene-2-one. It is easily purified by distilling through a Vigreux column (p 11) in a vacuum and taking the middle fraction. [Danishefsky & Kitihara J Am Chem Soc 96 7807 1974, Danishefsky Acc Chem Res 14 400 1981.]
Spectrum DetailBack Directory
[Spectrum Detail]

1-METHOXY-3-TRIMETHYLSILOXY-1,3-BUTADIENE(54125-02-9)1HNMR
1-METHOXY-3-TRIMETHYLSILOXY-1,3-BUTADIENE(54125-02-9)IR
1-METHOXY-3-TRIMETHYLSILOXY-1,3-BUTADIENE(54125-02-9)FT-IR
1-METHOXY-3-TRIMETHYLSILOXY-1,3-BUTADIENE(54125-02-9)Raman
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

1-Methoxy-3-trimethylsiloxy-1,3-butadiene, 98+%(54125-02-9)
[Sigma Aldrich]

54125-02-9(sigmaaldrich)
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