254819
Hydroquinidine hydrochloride
98%
Sinónimos:
Dihydroquinidine hydrochloride
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About This Item
Fórmula empírica (notación de Hill):
C20H26N2O2 · HCl
Número de CAS:
Peso molecular:
362.89
EC Number:
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22
Productos recomendados
Quality Level
assay
98%
form
powder
optical activity
[α]20/D +185.2°, c = 1.3 in H2O
mp
277-279 °C (lit.)
functional group
hydroxyl
SMILES string
Cl.CC[C@H]1CN2CC[C@H]1C[C@@H]2[C@@H](O)c3ccnc4ccc(OC)cc34
InChI
1S/C20H26N2O2.ClH/c1-3-13-12-22-9-7-14(13)10-19(22)20(23)16-6-8-21-18-5-4-15(24-2)11-17(16)18;/h4-6,8,11,13-14,19-20,23H,3,7,9-10,12H2,1-2H3;1H/t13-,14-,19+,20-;/m0./s1
InChI key
MULXTQKDWYBJMO-VJAUXQICSA-N
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Veronica Harvey et al.
Biomedical sciences instrumentation, 38, 185-190 (2002-06-28)
Recent research in our laboratories has been directed towards the development of ionomeric polymers and monomers for use in biomedical applications such as adhesives, drug delivery matrices and tissue scaffolds. The chemical Hydroquinone (HQ) aids as a stabilizer and represents
Yuanzhi Song et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 65(2), 333-339 (2006-03-11)
Geometric parameters, the vibrational frequencies and thermochemical values of benzoquinone and hydroquinone were computed using ab initio molecular orbital calculations (HF) and density function theory (B3LYP) methods with the 6-31G(d) basis set, respectively. The calculated frequencies for benzoquinone and hydroquinone
C Kirpizidis et al.
Journal of cardiology, 38(6), 351-354 (2002-01-25)
The effectiveness of oral quinidine for conversion of atrial fibrillation to sinus rhythm was evaluated in 49 patients with persistent atrial fibrillation on anticoagulation therapy. Atrial fibrillation was considered as persistent when the duration was longer than 3 days but
[Early repolarisation with ventricular fibrillation in a young woman].
Youssef Ben Ameur et al.
Presse medicale (Paris, France : 1983), 42(4 Pt 1), 474-479 (2012-09-11)
Aurélie Claraz et al.
The Journal of organic chemistry, 76(15), 6457-6463 (2011-06-18)
Herein is disclosed an efficient catalytic enantioselective protonation of enol acetates by means of a readily implementable transition-metal-free chemical process. By making use of simple hygrogenocarbonates as the proton source and hydroquinine anthraquinone-1,4-diyl diether as the chiral proton shuttle, a
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