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(S)-(+)-Epichlorohydrin

(S)-(+)-Epichlorohydrin

Product Description
CAT No.
ALN-N002014
CAS No.
67843-74-7
Mol. F.
C3H5ClO
Mol. Wt.
92.5
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RFQ
Chemical Name : (S)-2-(Chloromethyl)oxirane
Smiles : ClC[C@@H]1CO1
Inchi : InChI=1S/C14H18N4/c1-12-11-14(17-9-7-15-8-10-17)18(16-12)13-5-3-2-4-6-13/h2-6,11,15H,7-10H2,1H3

Nadolol: high-pressure liquid chromatographic methods for assay, racemate composition and related compounds

pauline m. lacroix,t norman m. curran and edward g. loveringnJournal of Pharmaceutical & Biomedical Analysis Vol. 10, Nos 10-12, pp. 917-924, 1992

The nonmetabolized u03b2u2011blocker nadolol is a substrate of oct1, oct2, mate1, mate2-k, and pu2011glycoprotein, but not of oatp1b1 and oatp1b3

Shingen Misaka, Jana Knop, Katrin Singer, Eva Hoier, Markus Keiser, Fabian Mu?ller, Hartmut Glaeser, Jo? rg Ko? nig, and Martin F. Fromm – Mol. Pharmaceutics 2016, 13, 2, 512–519

Separation of nadolol racemates by high pH reversed-phase preparative chromatography

Rami S. Arafaha,b , António E. Ribeiroa,b , Alírio E. Rodriguesc , Luís S. Pais – Separation and Purification Technology Volume 233, 15 February 2020, 116018

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