Recommended Products
form
solid
reaction suitability
reagent type: catalyst
mp
137-142 °C
SMILES string
[I-].Cn1c[n+](C)c2ccccc12
InChI
1S/C9H11N2.HI/c1-10-7-11(2)9-6-4-3-5-8(9)10;/h3-7H,1-2H3;1H/q+1;/p-1
InChI key
RQGURHMTNSNBQX-UHFFFAOYSA-M
Application
Catalyst for:
- Domino ring-opening redox amidation Knoevenagel condensation
- Intramolecular stereoselective protonation
- Grignard allylic substitution
- Acylation of alcohols
- Umpolung reactions
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Articles
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.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service