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B30200

Sigma-Aldrich

2-Benzylpyridine

98%

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About This Item

Empirical Formula (Hill Notation):
C12H11N
CAS Number:
101-82-6
Molecular Weight:
169.22
Beilstein:
115875
EC Number:
202-979-1
MDL number:
MFCD00006352
UNSPSC Code:
12352100
PubChem Substance ID:
24891680
NACRES:
NA.22

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.)

SMILES string

C(c1ccccc1)c2ccccn2

InChI

1S/C12H11N/c1-2-6-11(7-3-1)10-12-8-4-5-9-13-12/h1-9H,10H2

InChI key

PCFUWBOSXMKGIP-UHFFFAOYSA-N

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Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

257.0 °F - closed cup

Flash Point(C)

125 °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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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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