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| 2,6-DIISOPROPYL-N,N-DIMETHYLANILINE Basic information |
Product Name: | 2,6-DIISOPROPYL-N,N-DIMETHYLANILINE | Synonyms: | n,n-dimethyl-2,6-bis(1-methylethyl)-benzenamin;2,6-DIISOPROPYL-N,N-DIMETHYLANILINE;N,N-Dimethyl-2,6-diisopropylaniline.;2 6-DIISOPROPYL-N N-DIMETHYLANILINE 96%;2,6-Diisopropyl-N,N-dimethylaniline,97%;N,N-dimethyl-2,6-di(propan-2-yl)aniline;Benzenamine, N,N-dimethyl-2,6-bis(1-methylethyl)- | CAS: | 2909-77-5 | MF: | C14H23N | MW: | 205.34 | EINECS: | | Product Categories: | Building Blocks;C14 to C16;Amines;Chemical Synthesis;Nitrogen Compounds;Organic Building Blocks;C11 to C38;Nitrogen Compounds | Mol File: | 2909-77-5.mol | |
| 2,6-DIISOPROPYL-N,N-DIMETHYLANILINE Chemical Properties |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 26-36 | RIDADR | UN2810 | WGK Germany | 3 | TSCA | Yes | HazardClass | 6.1 | PackingGroup | III | HS Code | 29214200 |
| 2,6-DIISOPROPYL-N,N-DIMETHYLANILINE Usage And Synthesis |
Chemical Properties | clear colorless liquid | Uses | 2,6-Diisopropyl-N,N-dimethylaniline may be used as a co-initiator in two-photon polymerization. | General Description | 2,6-Diisopropyl-N,N-dimethylaniline (DIDMA) is a tertiary amine. It can undergo iron-catalyzed oxidative amidation with propionaldehyde (PrCHO) to form the corresponding hindered amide. |
| 2,6-DIISOPROPYL-N,N-DIMETHYLANILINE Preparation Products And Raw materials |
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