3-O--2-O-methyl-1-O-(octadecylcarbamoyl)glycerol

Base Information

Chemical Name:3-O--2-O-methyl-1-O-(octadecylcarbamoyl)glycerol
CAS No.:116953-44-7
Molecular Formula:C₃₂H₅₅N₃O₆
Molecular Weight:577.805
Hs Code.:

3-O-<N-acetyl-N-(2-pyridylmethyl)carbamoyl>-2-O-methyl-1-O-(octadecylcarbamoyl)glycerol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 3-O--2-O-methyl-1-O-(octadecylcarbamoyl)glycerol

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Technology Process of 3-O--2-O-methyl-1-O-(octadecylcarbamoyl)glycerol

There total 4 articles about 3-O--2-O-methyl-1-O-(octadecylcarbamoyl)glycerol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 80.0%

: 108-24-7
acetic anhydride

: 116953-38-9
2-O-methyl-3-O--1-O-(octadecylcarbamoyl)glycerol

: 116953-44-7,100488-81-1
3-O--2-O-methyl-1-O-(octadecylcarbamoyl)glycerol

Guidance literature:: With pyridine; at 110 ℃; for 72h;
DOI:10.1021/jm00121a012

Reference yield:

: 80350-03-4
3-(N-octadecylcarbamoyloxy)-2-methoxy-1-propanol

: 116953-44-7,100488-81-1
3-O--2-O-methyl-1-O-(octadecylcarbamoyl)glycerol

Guidance literature:: Multi-step reaction with 3 steps

1: 91 percent / pyridine / CH₂Cl₂ / 0.5 h / Ambient temperature

2: 100 percent / 1 h / 90 °C

3: 80 percent / pyridine / 72 h / 110 °C

With pyridine; In dichloromethane;
DOI:10.1021/jm00121a012

Reference yield:

: 3731-51-9
2-(Aminomethyl)pyridine

: 116953-44-7,100488-81-1
3-O--2-O-methyl-1-O-(octadecylcarbamoyl)glycerol

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / 1 h / 90 °C

2: 80 percent / pyridine / 72 h / 110 °C

With pyridine;
DOI:10.1021/jm00121a012