Quinoline-5-boronic acid

HCID 5153389CAS 355386-94-6

Daten werden ergänzt – meist innerhalb einer Minute fertig

Grundinformationen

Standard-SMILES
OB(O)c1cccc2ncccc12
InChIKey
NWIJBOCPTGHGIK-UHFFFAOYSA-N
Summenformel
C9H8BNO2
Durchschnittliche Molmasse
172,98 g/mol
Monoisotopische Masse
173,0648089

Namen und Bezeichner

Bevorzugter Name
Quinoline-5-boronic acid
IUPAC
Quinolin-5-ylboronic acid
Englischer Name
Quinoline-5-boronic acid
Summenformel
C9H8BNO2
Molmasse
172.98

Namen und Synonyme

QUINOLIN-5-YLBORONIC ACIDAKOS BRN-06815-BoronoquinolineCHEMBRDG-BB 42020925-QUINOLINBORONIC ACID5-Quinolylboronic Acid5-QUINOLINEBORONIC ACID5-Quinolinylboronic acidQUINOLINE-5-BORONIC ACIDQuionoline-5-Boronic Acid

Datenbank-Bezeichner

CAS
355386-94-6
PubChem CID
5153389
DTXSID
DTXSID90408935
EC Number
670-357-0
Nikkaji
J2.439.022E

Eigenschaften

Physikochemische Eigenschaften

Schmelzpunkt
144 · 144-148°C
Siedepunkt
400.3 · 400.3±37.0 °C(Predicted)
Dichte
1.28 · 1.28±0.1 g/cm3(Predicted)
storage temp.
Keep in dark place,Sealed in dry,Room Temperature
Aggregatzustand
powder to crystal
pka
7.46 · 7.46±0.30(Predicted)

Sicherheit und Regulatorisches

Sicherheitsdaten

hs_code
29334900
risk_code
36/37/38-36/38
hazard_code
Xi
safety_code
26-36-37/39-37
hazard_class
IRRITANT

Chemie und Industrie

Anwendungen · 1 Eintrag

VerwendenQuinoline-5-boronic acid is a fluorescent reporter compound that exhibits significant fluorescence property changes via a pKa-switching mechanism upon binding diols and carbohydrates in aqueous solutions at physiological pH[2]. Quinoline-5-boronic acid is used for monitoring sugars across a wide pH range, differentiating D-fructose from inulin, and functioning as a fluorescent probe for diols[2][3]. Quinoline-5-boronic acid is applied in fluorometric determination methods by combining with a phosphate buffer at neutral pH for selective D-fructose detection[3].

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