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536040

Sigma-Aldrich

4-4′-Dimethoxy-2-2′-bipyridine

greener alternative

97%

Synonym(s):

4,4′-Dimethoxy-2,2′-bipyridyl, 4,4′-Dimethoxy-2,2′-dipyridyl

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About This Item

Empirical Formula (Hill Notation):
C12H12N2O2
CAS Number:
Molecular Weight:
216.24
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

mp

168-171 °C (lit.)

greener alternative category

SMILES string

COc1ccnc(c1)-c2cc(OC)ccn2

InChI

1S/C12H12N2O2/c1-15-9-3-5-13-11(7-9)12-8-10(16-2)4-6-14-12/h3-8H,1-2H3

InChI key

IMEVSAIFJKKDAP-UHFFFAOYSA-N

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalysis. Find details here.

Application

4-4′-Dimethoxy-2-2'-bipyridine may be used as a ligand in the preparation of transition metal complexes.

Ligand for greener oxidation of alcohols under aerobic conditions.

Copper(I)/ABNO-Catalyzed Aerobic Alcohol Oxidation: Alleviating Steric and Electronic Constraints of Cu/TEMPO Catalyst Systems

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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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Synthesis and characterization of a new family of luminescent cis-(4, 4'-X2-5, 5'-Y2-2, 2'-bipyridine) 2Os (CO) Cl (PF6) complexes (X= NEt2, OMe, Me, H, Cl, Y= H; X= H, Y= Me; X= Y= Me): control of excited-state properties by bipyridyl substituents.
Della CL, et al.
Inorganic Chemistry, 29(15), 2792-2798 (1990)
Julie Urgiles et al.
Dalton transactions (Cambridge, England : 2003), 46(41), 14256-14263 (2017-10-11)
Reactions of K
Photochemical isomerization of trans- to cis-[RuCl2(dppb)(4,4'-X2-2,2'-bipy)](X=-H,-NO2,-Me,-COOH,-SMe,-O=SMe,-Cl,-OMe) complexes.
Santiago MO, et al.
Polyhedron, 22(24), 3205-3211 (2003)
Efficient osmium sensitizers containing 2,2'-bipyridine-4,4'-bisphosphonic acid ligand.
Zabri H, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 166(1), 99-106 (2004)
Katia M Oliveira et al.
Journal of inorganic biochemistry, 176, 66-76 (2017-09-04)
New Ru(II) complexes with lawsone (law) characterized as trans-[Ru(law)(PPh

Articles

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Arylboronic acids and esters, vital tools in chemical transformations, find extensive use, particularly in the Suzuki-Miyaura cross-coupling reaction.

Arylboronic acids and esters, vital tools in chemical transformations, find extensive use, particularly in the Suzuki-Miyaura cross-coupling reaction.

Arylboronic acids and esters, vital tools in chemical transformations, find extensive use, particularly in the Suzuki-Miyaura cross-coupling reaction.

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