Product: | (2R)-(2-Chloromethyl)oxirane | ||||
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Catalog Number: | 18314 | ||||
CAS Number: | 51594-55-9 | ||||
Synonyms: | (R)-(−)-Epichlorohydrin | ||||
Pricing: |
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Formula: | C3H5ClO | ||||
Molecular Weight: | 92.52 | ||||
Structure: | |||||
Appearance: | Clear liquid | ||||
Category: | API Compounds | ||||
Stability: | Stable under recommended storage conditions. | ||||
Storage: |
Keep container tightly closed in a dry and well-ventilated place. Containers which are opened must be carefully resealed and kept upright to prevent leakage. Store in cool place |
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Transportation: |
IATA: Hazard Class: 6.1; UN Number: UN2023; Packing Group: II; Shipping Name: Proper shipping name: Epichlorohydrin |
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Literature References: |
Discovery and structure–activity relationships of 2-benzylpyrrolidine-substituted aryloxypropanols as calcium-sensing receptor antagonists: Wu Yanga, Yufeng Wanga, Jacques Y. Robergea, Zhengping Mab, Yalei Liua, R. Michael Lawrencea, David P. Rotellaa, Ramakrishna Seethalab, Jean H.M. Feyenb and John K. Dickson Jr.a; Author Affliations: aDiscovery Chemistry, Bristol–Myers Squibb Pharmaceutical Research Institute, P.O. Box 5400, Princeton, NJ 08543-5400, USA; bMetabolic and Cardiovascular Drug Discovery, Bristol–Myers Squibb Pharmaceutical Research Institute, P.O. Box 5400, Princeton, NJ 08543-5400, USA |
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MSDS: | |||||
Description: |
Used in the synthesis of chiral morpholines and dioxanes via a Mitsunobu diol-cyclization. Chiral building block in the enantioselective synthesis of trans-2,4-disubstituted piperidines.: Building block for the synthesis of a key intermediate in the synthesis of stable PGI2 analogue UT-15 |