520535
2-Bromo-6-methoxypyridine
97%
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About This Item
Fórmula empírica (notación de Hill):
C6H6BrNO
Número de CAS:
Peso molecular:
188.02
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
97%
refractive index
n20/D 1.559 (lit.)
bp
206 °C (lit.)
density
1.53 g/mL at 25 °C (lit.)
SMILES string
COc1cccc(Br)n1
InChI
1S/C6H6BrNO/c1-9-6-4-2-3-5(7)8-6/h2-4H,1H3
InChI key
KMODISUYWZPVGV-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
219.9 °F - closed cup
flash_point_c
104.4 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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An efficient modular protocol for synthesizing a series of facial-capping tris-pyridyl ligands, based on the tris(2-pyridyl)methoxymethane backbone, has been developed which allows for systematic variations of the steric demands at the periphery of the ligand. The coordination chemistry of one
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European Journal of Organic Chemistry, 2, 235-254 (2004)
A convenient synthesis of cyclopenta [b] pyridin-2, 5-dione as a non-glycosidic cardiotonic agent.
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ARKIVOC (Gainesville, FL, United States), 7, 92-100 (2008)
Mohammed K Elmkaddem et al.
Chemical communications (Cambridge, England), 46(6), 925-927 (2010-01-29)
A copper(i) catalyzed amination reaction utilizing aqueous ammonia and operating under mild conditions is presented. This method was employed for the efficient synthesis of various aminopyridine derivatives bearing electron withdrawing and electron donating groups.
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