The melting point of methyl methoxy is -113 degrees Celsius. The boiling point of methyl methoxy is 7.4 degrees Celsius.
The melting point of methyl p-nitrobenzoate is approximately 78-80°C.
Methyl orange red at (and below) pH 3.1, turning yellow at pH 4.4 (and up)
79 degrees
The compound CH3O is called methoxy or methyl ether.
IUPAC nomenclature: Isobutyl methyl ether : 1-methoxy-2-methylpropane Methyl tert-butyl ether : 2-methoxy-2-methylpropane Resorcinol : 1,3-dihydroxybenzene Catechol : 1,2-dihydroxybenzene Isobutyl alcohol : 2-methyl-1-propanol or 2-methylpropan-1-ol Even more at http://www.scribd.com/doc/14024052/IUPAC-Nomenclature-Exercises-in-Organic-Chemistry prepared by aditya vardhan, the world famous chemist.
that is methyl propyl ether. aka methoxy propane. not methoxy propyl ether. methyl propyl ether has 1 oxygen. methoxy propyl ether has 2 oxygens.
2-hexanone3-hexanone2-methyl-3-pentanone3-methyl-2-pentanone4-methyl-2-pentanone3,3-dimethyl-2-butanone
methyl esters have very low melting points and they are volatile. so there melting points are difficult to obtain.
Methyl stearate is a saturated fatty acid methyl ester, while methyl oleate is an unsaturated fatty acid methyl ester. Methyl oleate has a higher degree of unsaturation due to a double bond in its carbon chain, making it more flexible and less rigid than methyl stearate. Additionally, methyl oleate may have different physical properties, such as a lower melting point, compared to methyl stearate.
Because the only force holding methyl substituted butane together is a very weak dispersion force and it is not very heavy so it pretty much wants to be a gas.
The boiling point of methyl alcohol (methanol) is 64.7oC.
This is the melting point.