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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

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

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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)
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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