3-(2-Furoyl)quinoline-2-carboxaldehyde - CAS 126769-01-5

Catalog:	BB006661
Product Name:	3-(2-Furoyl)quinoline-2-carboxaldehyde
CAS:	126769-01-5
Synonyms:	3-(furan-2-carbonyl)quinoline-2-carbaldehyde

Technical Data

Safety and Hazards

Patents

Literatures

Computed Properties

IUPAC Name:	3-(furan-2-carbonyl)quinoline-2-carbaldehyde
Description:	3-(2-Furoyl)quinoline-2-carboxaldehyde is a fluorogenic derivatizing reagent suitable for HPLC for high amine assays.
Molecular Weight:	251.24
Molecular Formula:	C15H9NO3
Canonical SMILES:	C1=CC=C2C(=C1)C=C(C(=N2)C=O)C(=O)C3=CC=CO3
InChI:	InChI=1S/C15H9NO3/c17-9-13-11(15(18)14-6-3-7-19-14)8-10-4-1-2-5-12(10)16-13/h1-9H
InChI Key:	PNCHURHVMDRFTR-UHFFFAOYSA-N
Boiling Point:	491.7 °C at 760 mmHg
Density:	1.326 g/cm³
MDL:	MFCD03427748
LogP:	2.87130

Publication Number	Title	Priority Date
CN-110658163-A	Method for monitoring reaction in synthesis of DNA coding compound	20180629
CN-109844538-A	For enhancing the composition and method of fluorescence	20160901
EP-3507603-A1	Compositions and methods for enhanced fluorescence	20160901
JP-2019531474-A	Compositions and methods for enhanced fluorescence	20160901
US-2018092993-A1	Compositions and methods for enhanced fluorescence	20160901

PMID	Publication Date	Title	Journal
22740458	20120701	A comparative study of LED-induced fluorescence and laser-induced fluorescence in SDS-CGE: application to the analysis of antibodies	Electrophoresis
22430180	20120301	Quantitative impurity analysis of monoclonal antibody size heterogeneity by CE-LIF: example of development and validation through a quality-by-design framework	Electrophoresis
20082778	20100118	Protein fingerprinting of Staphylococcus species by capillary electrophoresis with on-capillary derivatization and laser-induced fluorescence detection	Analytica chimica acta
19722209	20090901	Environmentally friendly surface modification of PDMS using PEG polymer brush	Electrophoresis
19249052	20090410	Fluorescein thiocarbamyl amino acids as internal standards for migration time correction in capillary sieving electrophoresis	Journal of chromatography. A

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Related Functional Groups

Carbonyl Compounds

[1427004-19-0]
DBCO-PEG4-NHS ester
[17746-05-3]
Undecanoyl chloride
[959574-98-2]
(3-Phenyl-1H-pyrazol-1-yl)acetic acid
[70199-62-1]
(4-Pyridyl)acetone Hydrochloride
[1018141-88-2]
1-(2-Cyanoethyl)-3-methyl-6-phenyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid
[2168559-63-3]
2-(6-Methyl-2-pyridyl)acetic Acid Hydrochloride

GHS Hazard Statement:	H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]
Precautionary Statement:	P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word:	Warning

Complexity:	357
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	251.058243149
Formal Charge:	0
Heavy Atom Count:	19
Hydrogen Bond Acceptor Count:	4
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	251.058243149
Rotatable Bond Count:	3
Topological Polar Surface Area:	60.2 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	2.7