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411 REFERENCE · Wikipedia

1,3,5-Trimethyl-1,3,5-triazinane

Reference material by Wikipedia contributors. This retains its source identity and is not 411 news reporting.

File:1,3,5-trimethyl-1,3,5-triazane.svg 1,3,5-Trimethyl-1,3,5-triazinane Hexahydro-1,3,5-trimethyl-s-triazine Hexahydro-1,3,5-trimethyl-1,3,5-triazine 1,3,5-Trimethyl-1,3,5-triazacyclohexane 1,3,5-Trimethylhexahydro-1,3,5-triazine 108-74-7 correct CAS 7664 203-612-8 correct FDA 91CT72PELC 7952 1S/C6H15N3/c1-7-4-8(2)6-9(3)5-7/h4-6H2,1-3H3 DPMZXMBOYHBELT-UHFFFAOYSA-N CN1CN(C)CN(C)C1 6 15 3 Colorless or white liquid 0.925 g/cm3 −27 155-160 02 05 07 08 Danger 226 302 314 317 335 373 412 210 233 240 241 242 243 260 261 264 264+265 270 271 272 273 280 301+317 301+330+331 302+352 302+361+354 303+361+353 304+340 305+354+338 316 317 319 321 330 333+317 362+364 363 370+378 403+233 403+235 405 501 1,3,5-Trimethyl-1,3,5-triazinane is an organic compound with the formula (CH3NCH2)3. It is a colorless liquid that is soluble in many organic solvents. Structurally, it is one of several related hexahydro-1,3,5-triazines, which typically result from the condensation reaction of amines and formaldehyde. It undergoes deprotonation by butyllithium to give a reagent that serves as a source of the formyl anion.V. Subramanian "1,3,5-Trimethyl-1,3,5-triazacyclohexane " e-EROS Encyclopedia of Reagents for Organic Synthesis 2007. 10.1002/047084289X.rn01037 References Category:Tertiary amines Category:Triazines Category:Methyl compounds