Other grades of this product :
| (S)-5-Benzyl-2-Mesityl-6,6-diMethyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-C][1,4]oxazin-2-iuM tetrafluoroborate Basic information |
| Product Name: | (S)-5-Benzyl-2-Mesityl-6,6-diMethyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-C][1,4]oxazin-2-iuM tetrafluoroborate | | Synonyms: | (S)-5-Benzyl-2-Mesityl-6,6-diMethyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-C][1,4]oxazin-2-iuM tetrafluoroborate;(5S)-5-benzyl-6,6-dimethyl-2-(2,4,6-trimethylphenyl)-5,8-dihydro-[1,2,4]triazolo[3,4-c][1,4]oxazin-4-ium | | CAS: | 925706-40-7 | | MF: | C23H28BF4N3O | | MW: | 449.2925328 | | EINECS: | | Product Categories: | | Mol File: | 925706-40-7.mol |
| (S)-5-Benzyl-2-Mesityl-6,6-diMethyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-C][1,4]oxazin-2-iuM tetrafluoroborate Chemical Properties |
| Melting point | 200-206°C | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C |
| (S)-5-Benzyl-2-Mesityl-6,6-diMethyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-C][1,4]oxazin-2-iuM tetrafluoroborate Usage And Synthesis |
| Uses | Catalyst for:- Intermolecular conjugate addition of alcohols to unsaturated ketones and esters
- Preparation of β-amino carbonyl compounds by N-heterocyclic carbene-catalyzed enantioselective Mannich reactions of a-aryloxyacetaldehydes with imines
- Asymmetric synthesis of cyclopentenes from allyl diketones by carbene-catalyzed intramolecular aldol reaction, lactonization, and carbon dioxide expulsion
- Preparation of esters via tandem oxidation of allylic/benzylic/propargyl alcohols or aldehyde
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| (S)-5-Benzyl-2-Mesityl-6,6-diMethyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-C][1,4]oxazin-2-iuM tetrafluoroborate Preparation Products And Raw materials |
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![(S)-5-Benzyl-2-Mesityl-6,6-diMethyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-C][1,4]oxazin-2-iuM tetrafluoroborate](/img/925706-40-7.jpg "(S)-5-Benzyl-2-Mesityl-6,6-diMethyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-C][1,4]oxazin-2-iuM tetrafluoroborate")
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