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HCID 1218Erstellt: 26. Oktober 2026

SK&F 81297

sk&f81297 · (±)-6-Chloro-PB · SKF 81297 hydrobromi · SKF 81297 HYDROBROMIDE · (+/-)-SKF-81297 HYDROBROMIDE · (±)-6-Chloro-PB hydrobromide · (+/-)-6-CHLORO-PB HYDROBROMIDE · (+-)-6-CHLORO-PB HYDROBROMIDE (+-)-SKF-8 1297, HCL

https://huagongshe.com/de/chemical/1218

Molekülstruktur von SK&F 81297

Identifikatoren & physikalische Daten

CAS No.71636-61-8
SummenformelC16H16ClNO2
Durchschnittliche Molmasse289,75 g/mol
Monoisotopische Masse289,08695643 g/mol
SMILESOc1cc2c(c(Cl)c1O)CCNCC2c1ccccc1
InChIKeyGHWJEDJMOVUXEC-UHFFFAOYSA-N
PubChem CID1218
ChEMBLCHEMBL353335
ChEBICHEBI:91517
EC No.635-324-7
DTXSIDDTXSID3043815

Chemische & physikalische Eigenschaften

XLogP2,7
Polarare Oberfläche (TPSA)52,5
H-Brücken-Donoren3
H-Brücken-Akzeptoren3
Frei drehbare Bindungen1
Schwere Atome20
Formalladung0
Komplexität322
LagerbedingungenDesiccate at +4°C
LöslichkeitH2O: 1.7 mg/mLH2O: 1.7mg/mLDMSO: >10mg/mLethanol: 6.3mg/mL
Aggregatzustandsolid
Farbegray
InChI1S/C16H16ClNO2.BrH/c17-15-11-6-7-18-9-13(10-4-2-1-3-5-10)12(11)8-14(19)16(15)20/h1-5,8,13,18-20H,6-7,9H21H
InChIKeyRMIJGBMRNYUZRG-UHFFFAOYSA-N
SMILESBr[H].Oc1cc2C(CNCCc2c(Cl)c1O)c3ccccc3

Sicherheit & Vorschriften

GHS-EinstufungWarningH315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 39 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard Classes and CategoriesSkin Irrit. 2 (100%)
Wassergefährdungsklasse (WGK)3
R-Sätze (R)36/37/38
GefahrensymboleXi
Sicherheitshinweise (S)22-26-36
Lagerklasse11 - Combustible Solids
GefahrenklasseEye Irrit. 2Skin Irrit. 2STOT SE 3

Anwendungen & Verwendung

Verwenden

(±)-6-Chloro-PB hydrobromide has been used as a dopamine D1 receptor (Drd1a) agonist to study the role of the drd1a-dopamine receptor inactivation of extracellular signalregulated protein kinase 1/2 (ERK1/2) in the wild-type and striatum of dopamine-depleted mice. It has also been used as a Drd1a agonist to identify the contribution of D1 (D1R)-like dopamine receptor signaling on learning and memory in Barnes maze in rats.