Khoom Taw qhia
| (R)-(-)-3-Hydroxytetrahydrofuran Cov ntaub ntawv yooj yim |
| Khoom npe: | (R)-(-)-3-Hydroxytetrahydrofuran |
| Synonyms: | (R)-(-)-TETRAHYDRO-3-FURANOL;(R)-(-)-3-HYDROXYTETRAHYDROFURAN;(R)-3-HYDROXYTETRAHYDROFURAN;(R)-(-){{10 }}HYDROXYTETRAHYDROFURANE;3-FURANOL, TETRAHYDRO-, (R);(R)-TETRAHYDROFURAN-3-OL;(3R)-Tetrahydrofuran-3-ol;(3R)-Tetrahydrofuran{{20} }}ol |
| CAS: | 86087-24-3 |
| MF: | C4H8O2 |
| MW: | 88.11 |
| EINECS: | 617-796-6 |
| Khoom Categories: | Furans; Lub Tsev Blocks rau HIV Protease InhibitorsChiral Building Blocks; Cawv, Hydroxy Esters thiab Derivatives; Cell Signaling Enzymes; Heterocyclic Building Blocks; HIV Protease Reagents & Lub Hnab Proteins; Chiral Compounds; Chiral; Tetrahydrofuran INTAD Series; |
| Mol File: | 86087-24-3.mol |
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| (R)-(-)-3-Hydroxytetrahydrofuran Chemical Properties |
| alpha | -18.5 º (c=2 MeOH) |
| Boiling point | 181 degree (lit.) |
| ceev | 1.097 g / mL ntawm 25 degree (lit.) |
| Refractive Index | n20 / D 1.45 hli (lit.) |
| Fp | 180 degree F |
| cia temp. | Khaws nyob rau hauv qhov chaw tsaus, kaw hauv qhuav, Chav Kub |
| solubility | Chloroform, Methanol (me ntsis) |
| pka ua | 14.49 ± 0.20 (Tshaj tawm) |
| daim ntawv | Ua kua |
| Specific Gravity | 1.097 |
| xim | Ntshiab xim tsis muaj xim |
| kev ua haujlwm kho qhov muag | [ ]20/D 18 degree , c=2.4 hauv methanol |
| InChI | InChI=1S/C4H8O2/c5-4-1-2-6-3-4/h4-5H,1-3H2/t4-/m1/s1 |
| InChIKey | XDPCNPCKDGQBAN-SCSAIBSYSA-N |
| SMILES | O1CC[C@@H](O)C1 |
| CAS DataBase Reference | 86087-24-3(CAS DataBase Reference) |
| Cov ntaub ntawv kev nyab xeeb |
| Hazard Codes | Xis |
| Risk Statements | 36/37/38 |
| Cov lus hais txog kev nyab xeeb | 26-36 |
| RIDADR | NA 1993 / PIB |
| WGK Germany | 3 |
| HS Code | 29321900 |
| MSDS Cov Ntaub Ntawv |
| Tus kws kho mob | Lus |
|---|---|
| SigmaAldrich | Lus Askiv |
| (R)-(-)-3-Hydroxytetrahydrofuran Siv Thiab Synthesis |
| Chemical Properties | Colorless rau lub teeb daj liqui |
| Siv | (R)-(-)-3-Hydroxytetrahydrofuran yog siv los ua tshuaj reactant nyob rau hauv cov synthesis ntawm kws tshuaj. Empagliflozin yog synthesized siv cov reactant |
| Siv | (R)-(-)-3-Hydroxytetrahydrofuran tuaj yeem siv los ua lub tsev thaiv hauv kev sib txuas ntawm cov muaj zog HIV protease inhibitors. |
| (R)-(-)-3-Hydroxytetrahydrofuran Kev Npaj Khoom Thiab Raw Khoom |
| Cov khoom nyoos | 3-Furanol, tetrahydro-, 3-acetate-->Dihydrofuran-3(2H)-one-->3-Hydroxytetrahydrofuran-->(R)-4-CHLORO-1,3-BUTANEDIOL-->(R)-(+)-1,2,4-BUTANETRIOL-->but-3-en-1-yl 4-methylbenzene-1-sulfonate-->(S)-1,2,4-Butanetriol-->2, 3-Dihydrofuran |
| Cov khoom npaj | Furan, tetrahydro-3-iodo-, (3S)--->(S)-3-P-MESYLOXYTETRAHYDROFURAN |
Cim npe nrov: (r)-(-)-3-hydroxytetrahydrofuran, Tuam Tshoj (r)-(-)-3-hydroxytetrahydrofuran manufacturers, lwm tus neeg, Hoobkas
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