CAS ID | 6342-56-9 |
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IUPAC Name | 1,1-dimethoxypropan-2-one |
Molecular Formula | C5H10O3 |
Molecular Weight | |
SMILES | CC(=O)C(OC)OC |
CAS ID | 6342-56-9 |
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IUPAC Name | 1,1-dimethoxypropan-2-one |
Molecular Formula | C5H10O3 |
Molecular Weight | |
SMILES | CC(=O)C(OC)OC |
80650 |
Synonym: 1,1-dimethoxyacetone, pyruvic aldehyde dimethyl acetal, 2-propanone, 1,1-dimethoxy, methylglyoxal dimethyl acetal, 1,1-dimethoxy-2-propanone, dimethoxymethyl methyl ketone, pyruvaldehyde dimethyl acetal, 1,1-dimethoxy acetone, dimethoxyacetone, pyruvaldehyde, 1-dimethyl acetal
Boiling Point | 141°C |
Color | Undesignated |
UN Number | 1993 |
Formula Weight | 118.13 |
Physical Form | Clear Liquid at 20°C |
Chemical Name or Material | Pyruvic Aldehyde Dimethyl Acetal |
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The dimethyl acetal structure improves stability by shielding the reactive aldehyde group, allowing pyruvic aldehyde dimethyl acetal to withstand oxidation and other unwanted side reactions during storage or complicated chemical operations.
Yes, pyruvic aldehyde dimethyl acetal is frequently a crucial precursor in pharmaceutical synthesis. Its dimethyl acetal structure guarantees regulated reactivity, allowing the building of complicated molecular frameworks for enhanced drug research.
Pyruvic aldehyde dimethyl acetal is essential in synthesising aromatic chemicals and flavouring agents. The dimethyl acetal structure promotes stability during reactions, resulting in high-quality, pure end products.
Pyruvic aldehyde dimethyl acetal is differentiated by its dual functionality. It combines a ketone and an aldehyde inside a dimethyl acetal structure, providing greater adaptability in chemical processes than simpler acetals.
Safety precautions, such as gloves and eyewear, are necessary when working with pyruvic aldehyde dimethyl acetal. Although its dimethyl acetal structure improves stability, exposure to high temperatures or incompatible substances can still result in undesirable reactions.