688487
2-Mesityl-2,5,6,7-tetrahydropyrrolo[2,1-c][1,2,4]triazol-4-ium chloride
97%
Sinônimo(s):
Bode Catalyst 3
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Ensaio
97%
Formulário
solid
adequação da reação
reagent type: catalyst
pf
200-205 °C
cadeia de caracteres SMILES
[Cl-].Cc1cc(C)c(c(C)c1)-[n+]2cn3CCCc3n2
InChI
1S/C14H18N3.ClH/c1-10-7-11(2)14(12(3)8-10)17-9-16-6-4-5-13(16)15-17;/h7-9H,4-6H2,1-3H3;1H/q+1;/p-1
chave InChI
KKBONGWVMVUYPA-UHFFFAOYSA-M
Categorias relacionadas
Aplicação
- Intermolecular hydroacylation of cyclopropenes
- Crossed acyloin condensations
- Domino ring-opening redox amidation Knoevenagel condensation
- Claisen rearrangement
- Lewis acid- and N-heterocyclic carbene-catalyzed cyclocondensation reaction
- Bode catalyst for enantioselective cyclizations
Informações legais
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Órgãos-alvo
Respiratory system
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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Artigos
Rovis has demonstrated that triazolium salt in the presence of a base can act as an N-heterocyclic carbene organocatalyst1 in highly enantioselective intramolecular Stetter reactions.
Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.
Conteúdo relacionado
Bode Group creates N-mesityl-NHC catalysts for enantioselective annulations and SnAP reagents for one-pot aldehyde conversion into N-heterocycles.
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