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Key Documents

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C89803

Sigma-Aldrich

4-Cyanobenzoic acid

99%

Sinónimos:

Terephthalic acid mononitrile

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About This Item

Fórmula lineal:
NCC6H4CO2H
Número de CAS:
619-65-8
Peso molecular:
147.13
Beilstein/REAXYS Number:
1862865
EC Number:
210-606-9
MDL number:
MFCD00002528
UNSPSC Code:
12352103
PubChem Substance ID:
24893119
NACRES:
NA.23

Quality Level

100

assay

99%

form

liquid crystal

mp

219-221 °C (dec.) (lit.)

SMILES string

OC(=O)c1ccc(cc1)C#N

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

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
STBJ7582
S46230
06612CH
S30517
19311PC

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V Arjunan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 78(5), 1449-1454 (2011-02-26)
The Fourier transform infrared (FTIR) and FT-Raman spectra of p-cyanobenzoic acid (CBA) have been recorded in the range 4000-400 and 4000-100 cm(-1), respectively. The complete vibrational assignment and analysis of the fundamental modes of the compound were carried out using
Wan-Yin Fang et al.
Chemistry, an Asian journal, 12(17), 2323-2331 (2017-07-13)
A one-pot Pd-catalyzed carbonylation of phenols into their corresponding aryl carboxylic acids and esters through the insertion of carbon monoxide has been developed. This procedure offers a direct synthesis of aryl carboxylic acids and esters from inexpensive and abundant starting
P Boudeville et al.
Journal of pharmaceutical sciences, 84(9), 1083-1089 (1995-09-01)
A new methodology of pH-metric data treatment was developed to extract the stoichiometry and the thermodynamic association constants of guest-cyclodextrin inclusion complexes in dilute aqueous solution when the guest is a participant in an acid-base equilibrium. pH-metric titration curves in
Lisa A Hoferkamp et al.
Environmental science & technology, 40(7), 2206-2212 (2006-05-02)
The reductive transformation of p-cyanonitrobenzene (pCNB) was investigated in laboratory batch slurries exhibiting dominant terminal electron accepting processes (TEAPs). Pseudo-first-order rate constants (k(obs)) were measured for the reduction of pCNB in nitrate-reducing, iron-reducing, sulfate-reducing, and methanogenic sediment slurries. Reduction was
Matthew Noestheden et al.
Bioorganic chemistry, 35(3), 284-293 (2007-02-24)
A recombinant VH single-domain antibody recognizing staphylococcal protein A was functionalized on reactive lysine residues with N-hydroxysuccimidyl-activated 4-cyanobenzoate. Surface plasmon resonance analysis of antibody-antigen binding revealed that modified and unmodified antibodies bound protein A with similar affinities. Raman imaging of
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