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721344

Sigma-Aldrich

1-Methyl-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester

97%

Synonym(s):

1,2,3,6-tetrahydro-1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-pyridine, 1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-methyl-1,2,3,6-tetrahydropyridine, 4,4,5,5-Tetramethyl-2-[1-methyl-1,2,5,6-tetrahydropyridin-4-yl]-1,3,2-dioxaborolane

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About This Item

Empirical Formula (Hill Notation):
C12H22BNO2
CAS Number:
Molecular Weight:
223.12
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

solid

mp

72-76 °C

storage temp.

2-8°C

SMILES string

CN1CCC(=CC1)B2OC(C)(C)C(C)(C)O2

InChI

1S/C12H22BNO2/c1-11(2)12(3,4)16-13(15-11)10-6-8-14(5)9-7-10/h6H,7-9H2,1-5H3

InChI key

SQMVRFXDBRYXFQ-UHFFFAOYSA-N

Application

1-Methyl-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester can be used as a substrate in the study of para-alkenylation reactions of toluene using thianthrene S-oxide and palladium catalyst.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Articles

The synthesis of biaryl compounds via the Suzuki–Miyaura coupling reaction has become more commonplace now that many arylboronic acids are readily available.

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