| Weight | 164.201 g/mol |
|---|---|
| Formula | C7H16O4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 6 |
1,1,3,3-Tetramethoxypropane (102-52-3)
1,1,3,3-TMP
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- Fluorescent malondialdehyde polymers from hydrolysed 1,1,3,3-tetramethoxypropane (Analytica Chimica Acta, 1977)
- Oxidation of 1,2,4-trimethylbenzene (TMB), 2,3,6-trimethylphenol (TMP) and 2-methylnaphthalene to 2,3,5-trimethylbenzoquinone (TMBQ) and menadione (vitamin K3) (Catalysis Today, 2011)
- Electrochemical oxidation of [Cr(CO)4(tmp)] to the low-spin Cr(I) species [Cr(CO)4(tmp)]+ (tmp=3,4,7,8-tetramethyl-1,10-phenanthroline): an IR, UVVis, and EPR spectroelectrochemical and DFT computational study of the accompanying changes in molecular and electronic structure (Inorganica Chimica Acta, 2001)
- Efficient Synthesis of Salicylates by Catalytic [3 + 3] Cyclizations of 1,3-Bis(silyl enol ethers) with 1,1,3,3-Tetramethoxypropane (Journal of Organic Chemistry, 2007)
- Condensation of ferrocene with 1,1,3,3-tetramethoxypropane (Journal of Organometallic Chemistry, 1969)
- Stereoselective Transacetalization of 1,1,3,3-Tetramethoxypropane andN-Benzoylaminodiols (European Journal of Organic Chemistry, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1,1,3,3-TMP
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SMILESCOC(CC(OC)OC)OC
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InChIKeyXHTYQFMRBQUCPX-UHFFFAOYSA-N
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Similar Compounds
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ethyl 2-(2-methyl-1,3-dioxolan-2-yl)acetate
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1,1,3,3-Tetramethoxypropane
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