1,1,3,3-Tetramethoxypropane

1,1,3,3-Tetramethoxypropane
Names
	Preferred IUPAC name 1,1,3,3-Tetramethoxypropane
	Other names 1,1,3,3-Tetrakis(methyloxy)propane; Malonaldehyde, bis(dimethyl acetal)
Identifiers
CAS Number	102-52-3 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL592723;
ChemSpider	59410;
ECHA InfoCard	100.002.762
EC Number	203-037-2;
PubChem CID	66019;
UNII	GUB3D2SV2S ;
CompTox Dashboard (EPA)	DTXSID4059255 ;
	InChI InChI=1S/C7H16O4/c1-8-6(9-2)5-7(10-3)11-4/h6-7H,5H2,1-4H3 Key: XHTYQFMRBQUCPX-UHFFFAOYSA-N;
	SMILES COC(CC(OC)OC)OC;
Properties
Chemical formula	C7H16O4
Molar mass	164.201 g·mol−1
Appearance	Colorless liquid
Density	0.9895 g/cm3
Boiling point	183 °C (361 °F; 456 K)
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H226
Precautionary statements	P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

1,1,3,3-Tetramethoxypropane is an organic compound with the formula CH₂(CH(OCH₃)₂)₂. A colorless liquid, it is a protected form of malondialdehyde, a usefully reactive reagent that has poor storage properties.^[1]

References

↑ V. Nair, C. L. O'Neil, P. G. Wang "Malondialdehyde", Encyclopedia of Reagents for Organic Synthesis, 2008, John Wiley & Sons, New York. doi:10.1002/047084289X.rm013.pub2 Article Online Posting Date: March 14, 2008

[eEROS-1] V. Nair, C. L. O'Neil, P. G. Wang "Malondialdehyde", Encyclopedia of Reagents for Organic Synthesis, 2008, John Wiley & Sons, New York. doi:10.1002/047084289X.rm013.pub2 Article Online Posting Date: March 14, 2008

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References