147753
4-Aminobenzonitrile
98%
Synonym(s):
4-Cyanoaniline
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Linear Formula:
H2NC6H4CN
CAS Number:
Molecular Weight:
118.14
Beilstein:
774507
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
98%
form
solid
mp
83-85 °C (lit.)
SMILES string
Nc1ccc(cc1)C#N
InChI
1S/C7H6N2/c8-5-6-1-3-7(9)4-2-6/h1-4H,9H2
InChI key
YBAZINRZQSAIAY-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Application
4-Aminobenzonitrile was used as derivatization reagent in capillary zone electrophoretic analysis of aldoses, ketoses and uronic acid. It was used in the synthesis of methacrylic monomers containing pendant azobenzene structures and polythiophenes containing an azobenzene moiety in the side-chain.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Muta. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
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’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Synthesis and characterization of novel azobenzene methacrylate monomers.
Nicolescu FA, et al.
Designed Monomers and Polymers, 12(6), 553-563 (2009)
Synthesis of azobenzene-containing polythiophenes and photoinduced anisotropy.
Aubertin F and Zhao Y.
Journal of Polymer Science: Part A, General Papers, 42(14), 3445-3455 (2004)
Ranjit Kulkarni et al.
Nature communications, 10(1), 3228-3228 (2019-07-22)
Fully-aromatic, two-dimensional covalent organic frameworks (2D COFs) are hailed as candidates for electronic and optical devices, yet to-date few applications emerged that make genuine use of their rational, predictive design principles and permanent pore structure. Here, we present a 2D
Piyali Bhanja et al.
ChemSusChem, 10(5), 921-929 (2017-01-07)
The new covalent organic framework material TDFP-1 was prepared through a solvothermal Schiff base condensation reaction of the monomers 1,3,5-tris-(4-aminophenyl)triazine and 2,6-diformyl-4-methylphenol. Owing to its high specific surface area of 651 m
Daniel Bouša et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(49), 17728-17738 (2015-10-24)
In the last decade, graphene and graphene derivatives have become some of the most intensively studied materials. Tuning of the electronic and electrochemical properties of graphene is of paramount importance. In this study, six diazonium-modified graphenes containing different functional groups
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