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Key Documents

147753

Sigma-Aldrich

4-Aminobenzonitrile

98%

Synonym(s):

4-Cyanoaniline

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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

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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.

Pictograms

Health hazardExclamation mark

Signal Word

Warning

Hazard 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’.

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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
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)
Isabella Rustighi et al.
Electrophoresis, 30(15), 2632-2639 (2009-07-22)
N-linked or O-linked glycans derived from glycoprotein processing carry, an N-acetylglucosamine or an N-acetylgalactosamine respectively, at their reducing termini. The presence of the N-acetylamino group on C-2 of reducing sugar residues has been reported to hamper the derivatization reaction with
[Benzonitrile and its derivatives: action of para-aminobenzonitrile on the cardiovascular system].
S L Cheav et al.
Annales pharmaceutiques francaises, 44(5), 363-372 (1986-01-01)

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