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1206163-56-5

1206163-56-5 Structure

1206163-56-5 Structure
IdentificationBack Directory
[Name]

1-Benzyl-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-indole
[CAS]

1206163-56-5
[Synonyms]

1-Benzylindole-5-boronicacidpinacolester,95%
(1-BENZYL-1H-INDOL-5-YL)BORONIC ACID PINACOL ESTER
1-benzyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indole
1-Benzyl-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-indole
1H-Indole, 1-(phenylmethyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
[Molecular Formula]

C21H24BNO2
[MDL Number]

MFCD11894320
[MOL File]

1206163-56-5.mol
[Molecular Weight]

333.232
Chemical PropertiesBack Directory
[Melting point ]

128-131°C
[storage temp. ]

-20°C Freezer
[solubility ]

Chloroform (Slightly), DMSO (Slightly)
[form ]

Solid
[color ]

Pale Red
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H312-H332
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

1-Benzylindole-5-boronic Acid Pinacol Ester acts as a reagent in the synthesis of 3,3-difluoro-2-oxindoles via electrophilic fluorination of indoles using N-fluorobenzenesulfonimide. Preparation of triazolopyridine compounds as JAK kinase inhibitors useful in the treatment of neurodegenerative and inflammatory diseases.
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