CAS No. 4048-38-2
2,3,5,6-Tetrafluorobenzyl alcohol
2,3,5,6-四氟苯甲醇
| Catalog No. | 121937 |
|---|---|
| Name | 2,3,5,6-Tetrafluorobenzyl alcohol |
| CAS | 4048-38-2 |
| Formula | C7H4F4O |
About 2,3,5,6-Tetrafluorobenzyl alcohol
2,3,5,6-Tetrafluorobenzyl alcohol is a chemical compound registered under CAS number 4048-38-2, with the molecular formula C7H4F4O and a molecular weight of about 180.1 g/mol. ChemForTech supplies 2,3,5,6-Tetrafluorobenzyl alcohol for laboratory research and bulk production; product code 121937. Send an inquiry for purity, packaging, price and lead time.
- CAS Number
- 4048-38-2
- Molecular Formula
- C7H4F4O
- Molecular Weight
- 180.1 g/mol
Applications
32-38 ° C melting point
The boiling point of 220-225 ° C
1.499 density
Floc point ° C 62
CAS DataBase 4084-38-2 (CAS) DataBase instead
Chemical properties is colorless solid insoluble in water, but soluble in benzene etc organic solvents.
Use hexafluoroacetone benzyl alcohol is health with pesticide four flubendazolum chrysanthemum ester intermediates.
Production methods its preparation method is to use hexafluoroacetone benzoic acid in ethylene glycol dimethyl ether add the NaBH4 in drops of ethylene glycol dimethyl ether solution, temperature, stir ℃ < 30 30min, then and dimethyl sulfate solution of ethylene glycol dimethyl ether in 50 ℃ reaction 1h, continue to react to the post-processing, 2h products.
The boiling point of 220-225 ° C
1.499 density
Floc point ° C 62
CAS DataBase 4084-38-2 (CAS) DataBase instead
Chemical properties is colorless solid insoluble in water, but soluble in benzene etc organic solvents.
Use hexafluoroacetone benzyl alcohol is health with pesticide four flubendazolum chrysanthemum ester intermediates.
Production methods its preparation method is to use hexafluoroacetone benzoic acid in ethylene glycol dimethyl ether add the NaBH4 in drops of ethylene glycol dimethyl ether solution, temperature, stir ℃ < 30 30min, then and dimethyl sulfate solution of ethylene glycol dimethyl ether in 50 ℃ reaction 1h, continue to react to the post-processing, 2h products.
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