ChemicalBook > Product Catalog > Chemical Reagents > Organic reagents > Esters > Methyl ester compound > Iodomethyl pivalate
Iodomethyl pivalate
Iodomethyl pivalate Basic information
- Product Name:
- Iodomethyl pivalate
- Synonyms:
-
- AURORA KA-7367
- IODOTOLUENE(4-)
- IODOMETHYL PIVALATE
- (Pivaloyloxy)Methyl Iodide
- 2,2-DiMethyl-propanoic Acid IodoMethyl Ester
- Iodomethyl Pivalate (stabilized with Copper chip)
- 2,2-dimethylpropionic acid iodomethyl ester
- iodomethyl 2,2-dimethylpropanoate
- CAS:
- 53064-79-2
- MF:
- C6H11IO2
- MW:
- 242.05
- EINECS:
- 258-339-7
- Product Categories:
-
- Miscellaneous Reagents
- Miscellaneous
- Mol File:
- 53064-79-2.mol
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Iodomethyl pivalate Chemical Properties
- Melting point:
- 33-35 °C(lit.)
- Boiling point:
- 211.5 °C(lit.)
- Density
- 1.614±0.06 g/cm3(Predicted)
- refractive index
- 1.4830 to 1.4870
- Flash point:
- 194 °F
- storage temp.
- Refrigerator, under inert atmosphere
- solubility
- Chloroform (Slightly), Methanol (Slightly)
- form
- Oil
- color
- Yellow
- Sensitive
- Light, Air and Heat Sensitive
- InChI
- InChI=1S/C6H11IO2/c1-6(2,3)5(8)9-4-7/h4H2,1-3H3
- InChIKey
- PELJISAVHGXLAL-UHFFFAOYSA-N
- SMILES
- C(OCI)(=O)C(C)(C)C
- CAS DataBase Reference
- 53064-79-2(CAS DataBase Reference)
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MSDS
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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Iodomethyl pivalate Usage And Synthesis
Chemical Properties
Pale Yellow Liquid
Uses
Iodomethyl pivalate can be used as reagent used for the addition of pivaloyl group.
Synthesis Reference(s)
The Journal of Organic Chemistry, 48, p. 5280, 1983 DOI: 10.1021/jo00174a024
Synthesis
Iodomethyl pivalate is synthesised using chloromethyl pivalate as a raw material by chemical reaction. The specific synthesis steps are as follows:
Three bottles were added 10.0 g of chloromethyl pivalate, Ethyl acetate 30 mL, 11.6 g of sodium iodide and 3.6 g of calcium chloride, After heating to 78 ° C for 6 h, Cooling to 0 ,Then washed with 5% sodium thiosulfate to colorless, Dried over anhydrous magnesium sulfate, Concentrated under reduced pressure. 16 g of a yellow liquid. Iodomethyl pivalate was obtained. The reaction molar yield was 94% and GC: 98%.
Iodomethyl pivalateSupplier
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