About This Item
Fórmula empírica (Notação de Hill):
C6H6BrN
Número CAS:
Peso molecular:
172.02
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Ensaio
95%
índice de refração
n20/D 1.568 (lit.)
p.e.
218-219 °C (lit.)
densidade
1.544 g/mL at 25 °C (lit.)
grupo funcional
bromo
cadeia de caracteres SMILES
Cc1cccnc1Br
InChI
1S/C6H6BrN/c1-5-3-2-4-8-6(5)7/h2-4H,1H3
chave InChI
PZSISEFPCYMBDL-UHFFFAOYSA-N
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Órgãos-alvo
Respiratory system
Código de classe de armazenamento
10 - Combustible liquids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
235.4 °F - closed cup
Ponto de fulgor (°C)
113 °C - closed cup
Equipamento de proteção individual
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Kelnner W R de França et al.
The Journal of organic chemistry, 67(6), 1838-1842 (2002-03-16)
2,2'-Bipyridine (bpy) and a series of dimethyl-2,2'-bipyridines were synthesized from 2-bromopyridine and 2-bromomethylpyridines, respectively, using an electrochemical process catalyzed by nickel complexes. The method is simple and efficient, with isolated yields between 58 and 98% according to the structure. We
Lynne H Thomas et al.
Acta crystallographica. Section C, Crystal structure communications, 69(Pt 11), 1279-1288 (2013-11-07)
Controlled introduction of proton transfer into the design of a series of molecular complexes is described, delivering the systematic production of ionic molecular complexes (molecular salts). The controlled production of molecular salts has relevance as a potential strategy in the
Synthesis of 2, 2'-Bipyridines: Versatile Building Blocks for Sexy Architectures and Functional Nanomaterials.
European Journal of Organic Chemistry, 2, 235-254 (2004)
Copper (ii) complexes of 2-halo-3-methylpyridine: synthesis, structure, and magnetic behaviour of Cu (2-X-3-CH 3 py) 2 X' 2 [X, X'= chlorine or bromine; py= pyridine].
Herringer SN, et al.
Dalton Transactions, 40(16), 4242-4252 (2011)
Alan C Spivey et al.
Organic letters, 9(5), 891-894 (2007-02-10)
[reaction: see text] The scope and limitations of the conjugate addition of 2- and the first 4-pyridyl Gilman homocuprates to various alpha,beta-unsaturated Michael acceptors are delineated. The conjugate addition of the cuprate of 2-bromo-3-methylpyridine to (E)-methyl crotonate then diastereoselective enolate
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