ChemicalBook--->CAS DataBase List--->50264-63-6

50264-63-6

50264-63-6 Structure

50264-63-6 Structure
IdentificationBack Directory
[Name]

1-[(4-Fluorophenyl)methyl]-1H-indazole-3-carboxylic acid
[CAS]

50264-63-6
[Synonyms]

AB-FUBINACA metabolite 4
1-(4-fluorobenzyl)-1H-indazole-3-carboxylic acid
1-[(4-fluorophenyl)methyl]indazole-3-carboxylic acid
1-[(4-Fluorophenyl)methyl]-1H-indazole-3-carboxylic acid
1H-Indazole-3-carboxylic acid, 1-[(4-fluorophenyl)methyl]-
[Molecular Formula]

C15H11FN2O2
[MDL Number]

MFCD01719717
[MOL File]

50264-63-6.mol
[Molecular Weight]

270.26
Chemical PropertiesBack Directory
[Melting point ]

194 °C(Solv: acetic acid (64-19-7))
[Boiling point ]

495.5±30.0 °C(Predicted)
[density ]

1.34±0.1 g/cm3(Predicted)
[solubility ]

DMF: 30 mg/mL; DMSO: 30 mg/mL; Ethanol: 30 mg/mL; PBS (pH 7.2): 0.10 mg/mL
[form ]

A crystalline solid
[pka]

3.06±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H332-H312
[Precautionary statements ]

P280-P302+P352-P312-P322-P363-P501-P264-P270-P301+P312-P330-P501-P261-P271-P304+P340-P312
[HS Code ]

2933998090
Hazard InformationBack Directory
[Description]

AB-FUBINACA metabolite 4 (Item No. 20179) is an analytical reference standard that is structurally classified as a synthetic cannabinoid. It is the carboxylic acid indazole 4-fluorobenzyl metabolite of AB-FUBINACA (Item Nos. 14039 | ISO60211). The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research applications.
[Uses]

1-[(4-Fluorophenyl)methyl]-1H-indazole-3-carboxylic Acid is used as a reactant in the preparaion of cannabinoid indole and indazole compounds for treating pain and nausea. Synthetic cannabinoids
[References]

[1] SAMUEL D. BANISTER. Pharmacology of Indole and Indazole Synthetic Cannabinoid Designer Drugs AB-FUBINACA, ADB-FUBINACA, AB-PINACA, ADB-PINACA, 5F-AB-PINACA, 5F-ADB-PINACA, ADBICA, and 5F-ADBICA[J]. ACS Chemical Neuroscience, 2015, 6 9: 1546-1559. DOI: 10.1021/acschemneuro.5b00112
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