147753
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
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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.
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)
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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
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Chemphyschem : a European journal of chemical physics and physical chemistry, 14(4), 728-740 (2012-12-05)
IR photodissociation (IRPD) spectra of mass-selected cluster ions of 4-aminobenzonitrile (ABN(+)) with up to four Ar and N2 ligands are recorded over the spectral range of the N-H stretching vibrations (ν(s/a)) of ABN(+) in its (2)B1 ground electronic state. ABN(+)-L(n)
H Schwaiger et al.
Electrophoresis, 15(7), 941-952 (1994-07-01)
Aldoses, ketoses and uronic acids were derivatized successfully within 15 min at a temperature of 90 degrees C by reductive amination with 4-aminobenzonitrile. Subsequently, the derivatives were separated as their borate complexes by capillary zone electrophoresis, using 175 mM borate
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