- 9-Anthracenemethanol
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- $0.00 / 1kg
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2024-09-24
- CAS:1468-95-7
- Min. Order: 1kg
- Purity: 98%+
- Supply Ability: 10000kgs per Month
- 9-Anthracenemethanol
-
- $0.00 / 1Kg
-
2024-09-23
- CAS:1468-95-7
- Min. Order: 1Kg
- Purity: 99.9%
- Supply Ability: 200tons
- 9-Anthracenemethanol
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- $0.00 / 1KG
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2024-09-18
- CAS:1468-95-7
- Min. Order: 1KG
- Purity: 98%min
- Supply Ability: 30tons/month
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| 9-Anthracenemethanol Basic information |
| 9-Anthracenemethanol Chemical Properties |
Melting point | 162-164 °C(lit.) | Boiling point | 307.46°C (rough estimate) | density | 1.0459 (rough estimate) | refractive index | 1.5361 (estimate) | storage temp. | Sealed in dry,Room Temperature | solubility | Soluble in hot methanol very faint turbidity. | form | Crystalline Powder | pka | 14.36±0.10(Predicted) | color | Yellow | BRN | 1873402 | Stability: | Stable. Incompatible with oxidizing agents. | InChIKey | JCJNNHDZTLRSGN-UHFFFAOYSA-N | CAS DataBase Reference | 1468-95-7(CAS DataBase Reference) | NIST Chemistry Reference | 9-Anthracenemethanol(1468-95-7) | EPA Substance Registry System | 9-Anthracenemethanol (1468-95-7) |
Risk Statements | 20/21/22-36/37/38 | Safety Statements | 24/25 | WGK Germany | 3 | RTECS | CB0577500 | TSCA | Yes | HS Code | 29062900 | Toxicity | mic-bac-sat 390 mmol/L CRNGDP 15,2605,94 |
| 9-Anthracenemethanol Usage And Synthesis |
Chemical Properties | It is a colorless or light yellow solid that is soluble in ordinary organic solvents. | Uses | An anthracene derivative used in Diels-Alder reactions. Also used in the preparation of 9-anthracenylmethyl-1-piperazinecarboxylate. | Uses | 9-Anthracenemethanol can be used: As a starting material to prepare 9-anthracenylmethyl-1-piperazinecarboxylate, which acts as a reagent in the determination of isocyanates using HPLC. In the Diels-Alder reaction with dimethylacetylene-dicarboxylate to yield lactone derivatives. As an initiator in the ring-opening polymerization of δ-valerolactone to yield poly(δ-valerolactone). As a starting material in the synthesis of polymer-supported anthracene, which acts as a dienophile scavenger in cycloaddition reactions. | Preparation | 9-Anthracenemethanol is synthesized by hydrogenation of 9-anthracenecarboxaldehyde. It is a versatile precursor to supramolecular assemblies. | General Description | 9-Anthracenemethanol participates in ring-opening polymerization of L-lactide catalyzed by alumoxane. It undergoes proton exchange reaction with potassium tert-butoxide to yield potassium 9-anthracenemethoxide. | Safety Profile | Mutation data reported. Whenheated to decomposition it emits acrid smoke andirritating vapors. |
| 9-Anthracenemethanol Preparation Products And Raw materials |
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