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Name: 18-tert-butoxy-18-oxooctadecanoic acid
CAS NO: 843666-40-0
MF: C22H42O4
MW: 370.57
MP: 68 ¡ãC
BP:470.7¡À18.0 ¡ãC(Predicted)
Density:0.950¡À0.06 g/cm3(Predicted)
Appearance: White powder
Purity: 99% min
Package: 25g, 100g, 500g, bulk package
Application:organic syntheses intermediate
Description of 18-tert-butoxy-18-oxooctadecanoic acid CAS NO: 843666-40-0
Name: 18-tert-butoxy-18-oxooctadecanoic acid
CAS NO: 843666-40-0
MF: C22H42O4
MW: 370.57
MP: 68 °C
BP:470.7±18.0 °C(Predicted)
Density:0.950±0.06 g/cm3(Predicted)
Appearance: White powder
Purity: 99% min
Package: 25g, 100g, 500g, bulk package
Application:organic syntheses intermediate
18-(Tert-butoxy)-18-oxooctadecanoic acid CAS NO: 843666-40-0 is a synthetic intermediate that has been used to synthesize semaglutide. It can be produced by the catalytic effect of ethyl bromoacetate on 18-hydroxyoctadecanoic acid in the presence of formamide and magnetic trifluoroacetic acid. The reaction time for the synthesis is 2 hours and produces high yields with a solid-phase synthesis. The product can be recycled, which reduces waste and cost. The product is also catalytically active and has a long shelf life.
Other name:
Octadecanedioicacid,mono(1,1-dimethylethyl) ester (9CI);
18-[(2-methylpropan-2-yl)oxy]-18-oxooctadecanoic acid;
Octadecanedioic acid mono-tert-butyl ester;
Application of 18-(Tert-butoxy)-18-oxooctadecanoic acid CAS NO: 843666-40-0
1.Synthesis of Radiopharmaceuticals
18-(Tert-butoxy)-18-oxooctadecanoic acid CAS NO: 843666-40-0 and its derivatives have been explored for the synthesis of radiopharmaceuticals, specifically as precursors in the synthesis of fluorine-18 labeled compounds.
2.Biolubricant Basestocks
365betÓéÀÖly modified plant oils, incorporating functional groups similar to those in 18-(Tert-butoxy)-18-oxooctadecanoic acid, have been synthesized to overcome the limitations of plant oils as industrial lubricants. Derivatives with improved low-temperature properties and thermal stability show potential as environmentally friendly biolubricant basestocks.
3.Polyoxotitanate Clusters
The controlled reaction between titanium tert-butoxide and acetic acid, involving compounds related to 18-(Tert-butoxy)-18-oxooctadecanoic acid, leads to the formation of new polyoxotitanate clusters.
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