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About This Item
Empirical Formula (Hill Notation):
C11H17BN2O2
CAS Number:
Molecular Weight:
220.08
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
Quality Level
assay
97%
form
solid
mp
131-135 °C (lit.)
SMILES string
CC1(C)OB(OC1(C)C)c2ccc(N)nc2
InChI
1S/C11H17BN2O2/c1-10(2)11(3,4)16-12(15-10)8-5-6-9(13)14-7-8/h5-7H,1-4H3,(H2,13,14)
InChI key
YFTAUNOLAHRUIE-UHFFFAOYSA-N
Application
Substrate used in a microwave-assisted, four-component coupling process leading to amino substituted imidazopyridines.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Erin F Dimauro et al.
The Journal of organic chemistry, 72(3), 1013-1016 (2007-01-27)
The rapid and efficient synthesis of various 2,6-disubstituted-3-amino-imidazopyridines using a microwave-assisted one-pot cyclization/Suzuki coupling approach is described. The utility of a 2-aminopyridine-5-boronic acid pinacol ester as a robust and versatile building block for the synthesis of diverse compound libraries is
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 640379-5G | 04061832880501 |
| 640379-1G | 04061826065570 |
