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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
- 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
Regulatory Listings
Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.
ISHL Indicated Name
Substances Subject to be Indicated Names
ISHL Notified Names
Substances Subject to be Notified Names
JAN Code
708593-VAR:
708593-250MG:4548173998596
708593-BULK:
708593-1G:4548173998589
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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.
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