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| | Ethyl (R)-(+)-4-chloro-3-hydroxybutyrate Basic information |
| | Ethyl (R)-(+)-4-chloro-3-hydroxybutyrate Chemical Properties |
| Melting point | 93-95 °C | | alpha | 14 º (neat) | | Boiling point | 93-95 °C/5 mmHg (lit.) | | density | 1.19 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.452 | | Fp | >110°C | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | Chloroform (Sparingly), DMSO (Slightly), Methanol (Slightly) | | pka | 13.23±0.20(Predicted) | | form | Oil | | color | Clear Colourless | | Specific Gravity | 1.190 | | optical activity | [α]23/D +14°, neat | | InChIKey | ZAJNMXDBJKCCAT-RXMQYKEDSA-N | | CAS DataBase Reference | 90866-33-4(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 41 | | Safety Statements | 26-36-36/39 | | RIDADR | 2810 | | WGK Germany | 3 | | HazardClass | 6.1 | | PackingGroup | III | | HS Code | 29181990 |
| | Ethyl (R)-(+)-4-chloro-3-hydroxybutyrate Usage And Synthesis |
| Chemical Properties | Colorless to light yellow liqui | | Uses | Ethyl (R)-(+)-4-chloro-3-hydroxybutyrate is a chiral building block that can be used:
- To prepare allyl stannane, a precursor for the total synthesis of macrolide iriomoteolide-1b.
- As a starting material for the synthesis of a chiral g-αmino acid fragment, which in turn is used to prepare the immunosuppressive agent FR252921.
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| | Ethyl (R)-(+)-4-chloro-3-hydroxybutyrate Preparation Products And Raw materials |
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