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CAS No. : | 42969-65-3 | MDL No. : | MFCD00211237 |
Formula : | C4H6O | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | GKPOMITUDGXOSB-SCSAIBSYSA-N |
M.W : | 70.09 | Pubchem ID : | 638102 |
Synonyms : |
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Signal Word: | Danger | Class: | 6.1,3 |
Precautionary Statements: | P201-P202-P210-P233-P240-P241-P242-P243-P260-P264-P270-P271-P272-P280-P284-P301+P310+P330-P303+P361+P353-P304+P340+P310-P305+P351+P338+P310-P308+P313-P333+P313-P370+P378-P403+P233-P403+P235-P405-P501 | UN#: | 2929 |
Hazard Statements: | H226-H300+H330-H315-H317-H318-H335-H351 | Packing Group: | Ⅱ |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
for 0.5h;Resolution of racemate; | General procedure: Thr-Phg (0.50 mmol) and alcohol (0.3 mL) were mixed in an agate mortar until an excessive amount of alcohol evaporated. After addition of alcohol (0.2 mL), the similar mixing was performed. It took about 30 min. The residual solids are collected and analyzed. The ratios of guest/host were determined by 1H NMR. After included alcohol was recovered by thermal decomposition of using a glass tube oven apparatus, the alcohol was reacted with phenylisocyanate to transform the N-phenylcarbamate. The enantiomeric excess was estimated as the N-phenylcarbamate by a chiral HPLC equipped with chiralcel OD-H or AD-H. |