- 1,3-Cyclohexanediol
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- $7.00 / 1KG
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2019-09-02
- CAS:504-01-8
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: JD 689
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| | 1,3-Cyclohexanediol Basic information |
| Product Name: | 1,3-Cyclohexanediol | | Synonyms: | 1,3-Cyclohexanedione99%;1,3-Cyclohexanediol, mixture of cis and trans, 98%;1,3-CYCLOHEXANEDIOL, (CIS- AND TRANS- MIXTURE) 99+%;1,3-Cyclohexanediol (cis- and trans- mixture);(1S)-Cyclohexane-1α,3β-diol;1,3-Dihydroxycyclohexane, Resorcitol;1,3-Cyclohexanediol, Mixture of cis and trans, 98% 10GR;1,3-Cyclohexanediol | | CAS: | 504-01-8 | | MF: | C6H12O2 | | MW: | 116.16 | | EINECS: | 207-979-5 | | Product Categories: | | | Mol File: | 504-01-8.mol |  |
| | 1,3-Cyclohexanediol Chemical Properties |
| Melting point | 30 °C | | Boiling point | 246-247 °C(lit.) | | density | 0.9958 (rough estimate) | | refractive index | 1.495-1.497 | | Fp | >230 °F | | form | Viscous Liquid After Melting | | pka | 14.70±0.40(Predicted) | | color | Clear slightly yellow | | Water Solubility | Soluble in water. | | BRN | 2036654 | | InChI | InChI=1S/C6H12O2/c7-5-2-1-3-6(8)4-5/h5-8H,1-4H2 | | InChIKey | RLMGYIOTPQVQJR-UHFFFAOYSA-N | | SMILES | C1(O)CCCC(O)C1 | | CAS DataBase Reference | 504-01-8(CAS DataBase Reference) | | NIST Chemistry Reference | 1,3-Cyclohexanediol(504-01-8) |
| Hazard Codes | Xi | | Risk Statements | 36/37 | | Safety Statements | 24/25-26 | | WGK Germany | 3 | | HS Code | 29061900 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Eye Irrit. 2
STOT SE 3 |
| | 1,3-Cyclohexanediol Usage And Synthesis |
| Chemical Properties | clear slightly yellow viscous liquid after melting | | Uses | 1,3-Cyclohexanediol is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields. | | Synthesis | General procedure: Example 3
To a reaction vessel, 510 mg (13.5 mmol) of sodium borohydride, 8 mL of tetrahydrofuran, 209 μL (1.63 mmol) of n-nonane, and 650 mg (6.8 mmol) of magnesium chloride were sequentially added, and the reaction mixture was stirred for 24 hours at room temperature. Subsequently, 9.8 mL of a tetrahydrofuran solution containing 1.11 g (9.9 mmol) of 1,3-cyclohexanedione was slowly added dropwise for 30 minutes. After the titration was completed, the reaction and post-treatment were carried out according to the method of Example 1. Upon completion of the reaction, the formation of cyclohexane-1,3-diol was confirmed by analysis in 97.5% yield. By-products included cyclohexanol (0.2%) and 2-cyclohexen-1-ol (1.2%). | | References | [1] Patent: US2003/149293, 2003, A1 |
| | 1,3-Cyclohexanediol Preparation Products And Raw materials |
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