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| IUPAC Name: | 1-chloro-N,N,2-trimethylprop-1-en-1-amine |
| Description: | 1-Chloro-N,N-2-trimethylpropenylamine (>90%) acts as a reagent in the synthesis and antitumor activity of (-)-bassianolide in human cancer cells through cell cycle arrest. Enantioselective total synthesis of nannocystins A and A0 as elongation factor 1 inhibitors. Total synthesis of (-)-caprazamycin A with antibacterial activity against Mycobacterium tuberculosis (TB) via diastereoselective aldol reaction. |
| Molecular Weight: | 133.62 |
| Molecular Formula: | C6H12ClN |
| Canonical SMILES: | CC(=C(N(C)C)Cl)C |
| InChI: | InChI=1S/C6H12ClN/c1-5(2)6(7)8(3)4/h1-4H3 |
| InChI Key: | GQIRIWDEZSKOCN-UHFFFAOYSA-N |
| Boiling Point: | 129-130 °C |
| Purity: | 95 % |
| Density: | 1.01 g/cm3 |
| Appearance: | Colorless to yellow liquid |
| Storage: | Freezer (-20 °C) |
| MDL: | MFCD00800562 |
| LogP: | 2.03820 |
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1-(4-Bromo-2-ethylpyrazol-3-yl)-N-methylmethanamine hydrochloride
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