B30200
2-苄基吡啶
98%
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关于此项目
经验公式（希尔记法）:
C12H11N
化学文摘社编号:
分子量:
169.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-979-1
Beilstein/REAXYS Number:
115875
MDL number:
产品名称
2-苄基吡啶, 98%
InChI key
PCFUWBOSXMKGIP-UHFFFAOYSA-N
InChI
1S/C12H11N/c1-2-6-11(7-3-1)10-12-8-4-5-9-13-12/h1-9H,10H2
SMILES string
C(c1ccccc1)c2ccccn2
assay
98%
form
liquid
refractive index
n20/D 1.579 (lit.)
bp
276 °C (lit.)
mp
8-10 °C (lit.)
density
1.054 g/mL at 25 °C (lit.)
Quality Level
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存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
257.0 °F - closed cup
flash_point_c
125 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Angelica E Graminha et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 69(4), 1073-1076 (2007-08-21)
Reaction of [RuCl(3)(dppb)H(2)O] (dppb=1,4 bis(diphenylphospine)butane) with 2-benzoylpyridine thiosemicarbazone (H2Bz4DH) and its N(4)-methyl (H2Bz4M) and N(4)-phehyl (H2Bz4Ph) derivatives gave [RuCl(dppb)(H2Bz4DH)]Cl (1), [RuCl(dppb)(H2Bz4M)]Cl (2) and [RuCl(dppb)(H2Bz4Ph)]Cl (3). The cytotoxic activity of the studied compounds was tested against the MCF-7, TK-10 and UACC-62
Masaki Itoh et al.
Organic letters, 16(7), 2050-2053 (2014-03-22)
The direct α-methylenation of benzylpyridines was achieved using N,N-dimethylacetamide (DMA) as a one-carbon source under copper catalysis. An intermediary species was detected at an early stage, and a possible mechanism was proposed. Additionally, α-oxygenation and dimerization of benzylpyridines could also
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