Droperidol

cas: 548-73-2 — see every product listed under this CAS number, including other names

Droperidol (CAS 548-73-2) is a chemical reagent available from Chemat. Available pack sizes: on request, 250mg, 10mg, 50mg, 10mM (in 1ml dmso), 1g, 2g, 5g. Offered by: Chemat Brand, Mikromol, LoGiCal, Dr. Ehrenstorfer.

brandChemat Brand
catalog numberAO-D0009.09
cas548-73-2
sizeon request
availability In stock
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Available pack sizes

brand size price
Chemat Brand on request price on request
Chemat Brand on request price on request
Mikromol 250mg price on request
LoGiCal 10mg price on request
Dr. Ehrenstorfer 50mg price on request
GLPBio 10mM (in 1ml dmso) 578.32 Pln
GLPBio 50mg 629.80 Pln
Biosynth 1g price on request
Biosynth 2g price on request
Biosynth 5g price on request
Biosynth 10g price on request
Biosynth 25g price on request
Sigma-Aldrich 1G 701.00 Pln
Sigma-Aldrich 1EA 665.70 Pln
Sigma-Aldrich 1ML 664.00 Pln
HPC Standards 1x50mg 488.86 Pln

properties

delivery timeTo be confirmed by Chemat
purityNo data
Structural formula: {0} (CAS {1})

Droperidol is an organofluorine compound that is haloperidol in which the hydroxy group has been eliminated with the introduction of a double bond in the piperidine ring, and the 4-chlorophenyl group has been replaced by a benzimidazol-2-on-1-yl group. It is used in the management of chemotherapy-induced nausea and vomiting, and in conjunction with an opioid analgesic such as fentanyl to maintain the patient in a calm state of neuroleptanalgesia with indifference to surroundings but still able to cooperate with the surgeon. It has a role as a dopaminergic antagonist, an antiemetic, an anaesthesia adjuvant and a first generation antipsychotic. It is a member of benzimidazoles, an organofluorine compound and an aromatic ketone.

Source: ChEBI

Identity
Molecular formulaC22H22FN3O2
Molecular weight379.4 g/mol
IUPAC name3-[1-[4-(4-fluorophenyl)-4-oxobutyl]-3,6-dihydro-2H-pyridin-4-yl]-1H-benzimidazol-2-one
InChIKeyRMEDXOLNCUSCGS-UHFFFAOYSA-N
SMILESC1CN(CC=C1N2C3=CC=CC=C3NC2=O)CCCC(=O)C4=CC=C(C=C4)F

Computed by PubChem (NCBI)

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