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710210

Sigma-Aldrich

(E)-3-(tert-Butyldimethylsilyloxy)propene-1-yl-boronic acid pinacol ester

97%

Synonym(s):

(E)-2-[3-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-1-propenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 2-[(1E)-3-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-1-propenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, tert-Butyldimethyl[[(2E)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)prop-2-en-1-yl]oxy]silane

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1 G
₩107,895
5 G
₩358,803

₩107,895

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1 G
₩107,895
5 G
₩358,803

About This Item

Empirical Formula (Hill Notation):
C15H31BO3Si
CAS Number:
114653-19-9
Molecular Weight:
298.30
MDL number:
MFCD15144803
UNSPSC Code:
12352103
PubChem Substance ID:
329762909
NACRES:
NA.22

₩107,895

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Quality Level

100

Assay

97%

form

liquid

density

0.910 g/mL at 25 °C

SMILES string

CC(C)(C)[Si](C)(C)OC\C=C\B1OC(C)(C)C(C)(C)O1

InChI

1S/C15H31BO3Si/c1-13(2,3)20(8,9)17-12-10-11-16-18-14(4,5)15(6,7)19-16/h10-11H,12H2,1-9H3/b11-10+

InChI key

LUURLZJMKOVITO-ZHACJKMWSA-N

Application

(E)-3-(tert-Butyldimethylsilyloxy)propene-1-yl-boronic acid pinacol ester can be used as a reactant in:
  • Palladium-catalyzed Suzuki-Miyaura coupling reaction.[1]
  • The synthesis of anti-homoallylic alcohols by allylation reaction with aldehydes in the presence of iridium complex-catalyst.[2]
  • The preparation of α-imino aldehydes.[3]

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
0000295286
0000246920
0000183410
0000189819
0000210073

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Palladium-catalyzed one-pot reaction of hydrazones, dihaloarenes, and organoboron reagents: Synthesis and cytotoxic activity of 1, 1-diarylethylene derivatives
Roche, M, et al.
The Journal of Organic Chemistry, 80(13), 6715-6727 (2015)
Enantioselective synthesis of anti homoallylic alcohols from terminal alkynes and aldehydes based on concomitant use of a cationic iridium complex and a chiral phosphoric acid
Miura T, et al.
Journal of the American Chemical Society, 135(31), 11497-11500 (2013)
Preparation of α-imino aldehydes by [1, 3]-rearrangements of O-alkenyl oximes
Kontokosta D, et al.
Organic Letters, 15(18), 4830-4833 (2013)

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