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D76722

Sigma-Aldrich

1,4-Dicyanobenzene

98%

Synonym(s):

Terephthalonitrile

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About This Item

Linear Formula:
C6H4(CN)2
CAS Number:
Molecular Weight:
128.13
Beilstein:
1072210
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

powder

mp

221-225 °C (lit.)

SMILES string

N#Cc1ccc(cc1)C#N

InChI

1S/C8H4N2/c9-5-7-1-2-8(6-10)4-3-7/h1-4H

InChI key

BHXFKXOIODIUJO-UHFFFAOYSA-N

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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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Customers Also Viewed

Felix Eberle et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 11(13), 2951-2956 (2010-08-18)
Self-assembled monolayers of 1,4-dicyanobenzene on Au(111) electrodes are studied by cyclic voltammetry, in-situ STM and ex-situ XPS. High-resolution STM images reveal a long-range order of propeller-like assemblies each of which consists of three molecules, all lying flat on the gold
Christian Ochsenfeld et al.
Solid state nuclear magnetic resonance, 22(2-3), 128-153 (2002-12-10)
A study of a host-guest system consisting of a naphthalene-spaced tweezer with a 1,4 dicyanobenzene guest molecule is presented. The complex is investigated using a combination of quantum-chemical calculations and solid-state NMR experiments. The advantages of such an approach are
T Sengupta et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 57A(5), 1103-1110 (2001-05-26)
The exciplex between all-s-trans-1,4-diphenylbuta-1,3-diene and 1,4-dicyanobenzene has been studied by steady state fluorescence along with the magnetic field effect (MFE) and compared with the other alpha,omega-diphenyl polyenes. The exciplex formation and magnetic field effect are dictated by the chain length
Suchandra Chatterjee et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 60(1-2), 97-102 (2003-12-13)
With the advent of spin chemistry, magnetic field effect (MFE) on exciplex luminescence has emerged as an important domain of research. MFE is a diffusion controlled phenomenon and hence is solvent dielectric (epsilon) dependent. It maximizes at a particular epsilon
Liheng Feng et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 68(3), 646-650 (2007-03-31)
A novel luminescent metal complex, (MQPF)3Al2, with 8-hydroxyquinoline aluminum and 9,9-diphenylfluorene was synthesized. The optical properties were investigated by UV-vis absorption and fluorescence emission spectra. The results showed that the luminescence quantum yield of (MQPF)3Al2 was 0.612 in THF and

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