Skip to Content
MilliporeSigma
All Photos(2)

Key Documents

View All Documentation

B30200

Sigma-Aldrich

2-Benzylpyridine

98%

Sign Into View Organizational & Contract Pricing
All Photos(2)

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

Looking for similar products? Visit Product Comparison Guide

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 3

1 of 3

2,2′-Bipyridine GR for analysis (reagent for iron(II) and molybdenum) ACS

Supelco

1.03098

2,2′-Bipyridine

Acetal ≥98%, FG

Sigma-Aldrich

W200204

Acetal

2-Methylpyridine 98%

Sigma-Aldrich

109835

2-Methylpyridine

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service