C89803
4-Cyanobenzoic acid
99%
Synonym(s):
Terephthalic acid mononitrile
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About This Item
Linear Formula:
NCC6H4CO2H
CAS Number:
Molecular Weight:
147.13
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
210-606-9
Beilstein/REAXYS Number:
1862865
MDL number:
Product Name
4-Cyanobenzoic acid, 99%
InChI
1S/C8H5NO2/c9-5-6-1-3-7(4-2-6)8(10)11/h1-4H,(H,10,11)
InChI key
ADCUEPOHPCPMCE-UHFFFAOYSA-N
SMILES string
OC(=O)c1ccc(cc1)C#N
assay
99%
form
liquid crystal
mp
219-221 °C (dec.) (lit.)
Quality Level
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Related Categories
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
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James Turkson et al.
Molecular cancer therapeutics, 3(3), 261-269 (2004-03-18)
The critical role of signal transducer and activator of transcription 3 (Stat3) in the growth and survival of human tumor cells identifies it as a promising target for cancer drug discovery. We previously identified a Stat3 SH2 domain-binding phosphopeptide, PY*LKTK
Federico Polo et al.
Journal of the American Chemical Society, 127(2), 492-493 (2005-01-13)
The rate constant of intramolecular electron transfer through oligopeptides based on the alpha-aminoisobutyric acid residue was determined as a function of the peptide length and found to depend weakly on the donor-acceptor separation. By measuring the electron-transfer activation energy and
Daniel L Kirschner et al.
Analytical chemistry, 79(2), 736-743 (2007-01-16)
A capillary electrophoresis method with laser-induced fluorescence detection for the chiral separation of cyanobenz[f]isoindole (CBI) derivatives of amino acids was developed and optimized. The enantioseparations are accomplished with sulfated beta-CD (S-beta-CD) as chiral selector at low pH and reverse polarity.
Qiao Chen et al.
Journal of protein chemistry, 22(7-8), 607-612 (2004-01-13)
Mushroom tyrosinase (EC 1.14.18.1), a copper containing oxidase, catalyzes both the hydroxylation of tyrosine into o-diphenols and the oxidation of o-diphenols into o-quinones. In the current study, the effects of 4-cyanobenzaldehyde and 4-cyanobenzoic acid on the monophenolase and diphenolase activities
Silverio Coco et al.
Dalton transactions (Cambridge, England : 2003), (48)(48), 6894-6900 (2008-12-04)
Gold complexes of 4-isocyanobenzoic acid, [AuX(CNC(6)H(4)CO(2)H)] (X = C[triple bond]C-C(6)H(4)-C(9)H(19), C(6)F(5), C(6)F(4)OC(6)H(13), C(6)F(4)C(6)F(4)Br) and [(mu-4,4'-C(6)F(4)C(6)F(4)){Au(CNC(6)H(4)CO(2)H)}(2)], have been isolated. These metallo-acids are luminescent. The single crystal X-ray diffraction study of [Au(C(6)F(5))(CNC(6)H(4)CO(2)H)](infinity) confirms a rod-like structure of the molecule, with a linear
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