5-(trichloromethyl)-4,5-dihydroisoxazol-5-ol
Modify Date: 2025-08-25 10:12:36
5-(trichloromethyl)-4,5-dihydroisoxazol-5-ol structure
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Common Name | 5-(trichloromethyl)-4,5-dihydroisoxazol-5-ol | ||
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| CAS Number | 34648-11-8 | Molecular Weight | 204.43900 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C4H4Cl3NO2 | Melting Point | 138-143 °C | |
| MSDS | N/A | Flash Point | N/A | |
| Name | 5-(trichloromethyl)-4H-1,2-oxazol-5-ol |
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| Synonym | More Synonyms |
| Melting Point | 138-143 °C |
|---|---|
| Molecular Formula | C4H4Cl3NO2 |
| Molecular Weight | 204.43900 |
| Exact Mass | 202.93100 |
| PSA | 41.82000 |
| LogP | 0.88690 |
|
~78%
5-(trichloromet... CAS#:34648-11-8 |
| Literature: Martins, Marcos A.P; Beck, Paulo; Cunico, Wilson; Pereira, Claudio M.P; Sinhorin, Adilson P; Blanco, Rogerio F; Peres, Rodrigo; Bonacorso, Helio G; Zanatta, Nilo Tetrahedron Letters, 2002 , vol. 43, # 39 p. 7005 - 7008 |
|
~82%
5-(trichloromet... CAS#:34648-11-8 |
| Literature: Rosa, Fernanda A.; Machado, Pablo; Bonacorso, Helio G.; Zanatta, Nilo; Martins, Marcos A. P. Journal of Heterocyclic Chemistry, 2008 , vol. 45, # 3 p. 879 - 885 |
|
~%
5-(trichloromet... CAS#:34648-11-8 |
| Literature: Spiegler; Gotz Synthesis, 1986 , vol. NO. 1, p. 69 - 70 |
|
~%
5-(trichloromet... CAS#:34648-11-8 |
| Literature: Platoshkin,A.M. et al. Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1971 , vol. 20, p. 1903 - 1907 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1971 , vol. 20, p. 2018 - 2024 |
| Precursor 2 | |
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| DownStream 1 | |
CAS#:21169-71-1| HS Code | 2934999090 |
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| Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
| 5-isoxazolol,4,5-dihydro-5-(trichloromethyl) |
| 5-hydroxy-5-trichloromethyl-4,5-dihydroisoxazole |
| 5-trichloromethyl-5-hydroxy-4,5-dihydroisoxazole |
| 5-(trichloromethyl)-4,5-dihydroisoxazol-5-ol |
| 5-trichloromethyl-2-isoxazolin-5-ol |
| 4,4,4-trichloro-3-oxo-butyraldehyde (Z)-oxime cyclo-tautomer |