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CAS Number: 78-26-2; PubChem CID: 66220; ChemSpider: 59605; UNII: YLM5KRU0P4; ... 2-Methyl-2-propyl-1,3-propanediol (MPP) is a simple alkyl diol which has sedative, ...
Meprobamate, 2-methyl-2-propyl-1,3-propanediol dicarbamate is synthesized by the reaction of 2-methylvaleraldehyde with two molecules of formaldehyde and the subsequent transformation of the resulting 2-methyl-2-propylpropan-1,3-diol into the dicarbamate via successive reactions with phosgene and ammonia.
Propylene glycol (IUPAC name: propane-1,2-diol) is a viscous, colorless liquid. It is almost odorless and has a faintly sweet taste. Its chemical formula is CH 3 CH(OH)CH 2 OH. As it contains two alcohol groups, it is classified as a diol. An aliphatic diol may also be called a glycol.
2,2-Disubstituted propane-1,3-diols are prepared in this way. Examples include 2-methyl-2-propyl-1,3-propanediol and neopentyl glycol. 1,3-Diols can be prepared by hydration of α,β-unsaturated ketones and aldehydes. The resulting keto-alcohol is hydrogenated. Another route involves the hydroformylation of epoxides followed by hydrogenation of ...
CH 3 CHCH 2 O + CO 2 → CH 3 C 2 H 3 O 2 CO. The corresponding reaction of 1,2-propanediol with phosgene is complex, yielding not only propylene carbonate but also oligomeric products. Propylene carbonate can also be synthesized from urea and propylene glycol over zinc acetate. [6]
2-Methyl-2-propyl-1,3-propanediol; Prenderol (2,2-diethyl-1,3-propanediol) References This page was last edited on 29 November 2024, at ...
2-Methyl-2-propyl-1,3-propanediol This page was last edited on 31 March 2023, at 01:35 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...
2-methylpropane-1,2-diol; 2-methylpropane-1,3-diol; and one unstable geminal diol: 2-methylpropane-1,1-diol (not a glycol), hydrate of 2-methylpropanal (isobutyraldehyde) These three methylpropanediols are structural isomers of butanediols. They are not chiral.
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