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520535

Sigma-Aldrich

2-Bromo-6-methoxypyridine

97%

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About This Item

Empirical Formula (Hill Notation):
C6H6BrNO
CAS Number:
40473-07-2
Molecular Weight:
188.02
MDL number:
MFCD00088345
UNSPSC Code:
12352100
PubChem Substance ID:
24874145
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

100

Assay

97%

refractive index

n20/D 1.559 (lit.)

bp

206 °C (lit.)

density

1.53 g/mL at 25 °C (lit.)

functional group

bromo

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

219.9 °F - closed cup

Flash Point(C)

104.4 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKBW0752V
MKBS4025V
MKBN4665V
MKBL4468V
MKBD9709V

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Robert T. Jonas et al.
Inorganic chemistry, 37(26), 6615-6629 (2001-10-24)
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
Synthesis of 2, 2'-Bipyridines: Versatile Building Blocks for Sexy Architectures and Functional Nanomaterials.
Newkome GR, et al.
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.
Robert N, et al.
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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