Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

I160

Sigma-Aldrich

3-(1H-Imidazol-4-yl)propyl di(p-fluorophenyl)methyl ether hydrochloride

powder

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C19H18F2N2O · HCl
Molecular Weight:
364.82
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

form

powder

color

pale gray

solubility

H2O: >4 mg/mL
methanol: 50 mg/mL
DMSO: 7 mg/mL

SMILES string

Cl.Fc1ccc(cc1)C(OCCCc2c[nH]cn2)c3ccc(F)cc3

InChI

1S/C19H18F2N2O.ClH/c20-16-7-3-14(4-8-16)19(15-5-9-17(21)10-6-15)24-11-1-2-18-12-22-13-23-18;/h3-10,12-13,19H,1-2,11H2,(H,22,23);1H

InChI key

LCHACRBDLUKTTM-UHFFFAOYSA-N

Gene Information

human ... HRH3(11255)

Biochem/physiol Actions

H3 histamine receptor antagonist.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

H Stark et al.
Die Pharmazie, 52(7), 495-500 (1997-07-01)
This study was performed in order to develop new leads for antagonists of the histamine H3-receptor subtype. omega-(1 H-Imidazol-4-yl)alkyl derivatives with ester, ketone or alcohol functionality in the side chain were synthesized and tested concerning their H3-receptor antagonist activity on
Diphenylmethyl ethers: Synthesis and histamine H3-receptor antagonist in vitro and in vivo activity.
Huls, A., et al.
Bioorganic & Medicinal Chemistry Letters, 6, 2013-2018 (1996)
Novel histamine H3-receptor antagonists with benzyl ether structure or related moieties: Synthesis and structure-activity relationships.
Huls, A., et al.
Archives of Pharmacal Research, 329, 379-379 (1996)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service