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903183

Sigma-Aldrich

Benzyl 4-oxo-3-(triethylsilyl)piperidine-1-carboxylate

≥95%

Synonym(s):

Garg silyl triflate precursor

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About This Item

Empirical Formula (Hill Notation):
C19H29NO3Si
CAS Number:
2242532-80-3
Molecular Weight:
347.52
UNSPSC Code:
12352005

Assay

≥95%

form

liquid

refractive index

n/D 1.528

density

1.082 g/mL

storage temp.

−20°C

Application

Benzyl 4-oxo-3-(triethylsilyl)piperidine-1-carboxylate is a precursor to a Garg silyl triflate which upon exposure to fluoride generates a reactive azacyclic allene for cycloaddition reactions.

Other Notes

Diels–Alder Cycloadditions of Strained Azacyclic Allenes

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

257.9 °F

Flash Point(C)

125.5 °C

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

903183-250MG:
903183-BULK:
903183-VAR:

Certificates of Analysis (COA)

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Joyann S Barber et al.
Nature chemistry, 10(9), 953-960 (2018-08-01)
For over a century, the structures and reactivities of strained organic compounds have captivated the chemical community. Whereas triple-bond-containing strained intermediates have been well studied, cyclic allenes have received far less attention. Additionally, studies of cyclic allenes that bear heteroatoms

Related Content

Garg Group – Professor Product Portal

The Garg group develops methods for the synthesis of natural products and pharmaceuticals. One key method pertains to heterocyclic arynes, such as indolynes and pyridynes, which are generated in situ from silyltriflate precursors under mild fluoride based reaction conditions.

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