902047
Pyridine-2,6-bis(carboximidamide) dihydrochloride
≥95%
Sinônimo(s):
Weix 2-pyridylcarboxamidine ligand for nickel catalysis
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250 MG
R$ 380,00
1 G
R$ 1.139,00
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250 MG
R$ 380,00
1 G
R$ 1.139,00
About This Item
Fórmula empírica (Notação de Hill):
C7H11Cl2N5
Número CAS:
Peso molecular:
236.10
Número MDL:
Código UNSPSC:
12352101
NACRES:
NA.22
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Ensaio
≥95%
Formulário
powder or crystals
adequação da reação
core: nickel
reaction type: Cross Couplings
reagent type: catalyst
cadeia de caracteres SMILES
Cl.Cl.NC(=N)c1nc(ccc1)C(=N)N
InChI
1S/C7H9N5.2ClH/c8-6(9)4-2-1-3-5(12-4)7(10)11;;/h1-3H,(H3,8,9)(H3,10,11);2*1H
chave InChI
YLMVDWSPWFNTRJ-UHFFFAOYSA-N
Categorias relacionadas
Aplicação
This pyridyl carboxamidine ligand has been demonstrated by Daniel Weix′s lab to enable nickel-catalyzed cross-coupling of diverse basic nitrogen heterocycles with primary and secondary alkyl halides.
Outras notas
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
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Eric C Hansen et al.
Nature chemistry, 8(12), 1126-1130 (2016-11-23)
Ligands are essential for controlling the reactivity and selectivity of reactions catalysed by transition metals. Access to large phosphine ligand libraries has become an essential tool for the application of metal-catalysed reactions industrially, but these existing libraries are not well
Eric C Hansen et al.
The Journal of organic chemistry, 82(14), 7085-7092 (2017-07-07)
Despite their importance, the synthesis of alkylated heterocycles from the cross-coupling of Lewis basic nitrogen heteroaryl halides with alkyl halides remains a challenge. We report here a general solution to this challenge enabled by a new collection of ligands based
Robert J Perkins et al.
Organic letters, 19(14), 3755-3758 (2017-07-14)
A constant-current electrochemical method for reducing catalytic nickel complexes in sp2-sp3 cross-electrophile coupling reactions has been developed. The electrochemical reduction provides reliable nickel catalyst activation and turnover and offers a tunable parameter for reaction optimization, in contrast to more standard
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