| Weight | 104.149 g/mol |
|---|---|
| Formula | C5H12O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
2,2-DIMETHOXYPROPANE (77-76-9)
Score:
#2078 in Physics
,
#5016 in Biology
,
#6465 in Chemistry
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- Acetonation of some pentoses with 2,2-dimethoxypropane-N,N-dimethylformamide-p-toluenesulfonic acid (Carbohydrate Research, 1976)
- The behavior of some aldoses with 2,2-dimethoxypropane-N,N-dimethylformamide-p-toluenesulfonic acid : I. At room temperature (25) (Carbohydrate Research, 1973)
- The preparation of anhydrous metal compounds by dehydration with 2,2-dimethoxypropane (Journal of Inorganic and Nuclear Chemistry, 1959)
- The Methyl Esterification of Amino Acids with 2,2-Dimethoxypropane and Aqueous Hydrogen Chloride1 (Journal of Organic Chemistry, 1963)
- Preparation of carbohydrate isopropylidene derivatives with 2,2-dimethoxypropane in the presence of toluene-p-sulphonic acid (Carbohydrate Research, 1981)
- Preparing Living Pollen Material for Scanning Electron Microscopy Using 2, 2-Dimethoxypropane (DMP) and Critical-Point Drying (Biotechnic & Histochemistry, 1998)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)(OC)OC
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InChIKeyHEWZVZIVELJPQZ-UHFFFAOYSA-N
- Pubchem - 2,2-DIMETHOXYPROPANE
- Wikipedia - 2,2-dimethoxypropane
2,2-Dimethoxypropane (DMP) is an organic compound with the formula]] (CH3)2C(OCH3)2. A colorless liquid, it is the product of the reaction of acetone and methanol. DMP is commonly used as a water scavenger in water-sensitive reactions.
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Similar Compounds
2,2-DIETHOXYPROPANE
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3,3-Dimethoxybutan-2-one
(21983-72-2)
1 alternate name
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(94158-44-8)
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tert-Butyl Isobutyl ether
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2,2-DIMETHOXYPROPANE
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