| Weight | 132.159 g/mol |
|---|---|
| Formula | C6H12O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Solketal (100-79-8)
2,2-dimethyl-1,3-dioxolane-4-methanol, (S)-isomer · 2,2-dimethyl-1,3-dioxolane-4-methanol, (R)-isomer · 2,2-dimethyl-1,3-dioxolane-4-methanol, (DL)-isomer
Score:
#2 in Energy and fuel
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#184 in Environmental science
,
#3608 in Biology
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#4529 in Chemistry
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- Acetalisation of bio-glycerol with acetone to produce solketal over sulfonic mesostructured silicas (Green Chemistry, 2010)
- Peripheral and Axial Substitution of Phthalocyanines with Solketal Groups: Synthesis and In Vitro Evaluation for Photodynamic Therapy (Journal of Medicinal Chemistry, 2007)
- Comparative studies of photophysical and photochemical properties of solketal substituted platinum(II) and zinc(II) phthalocyanine sets (Tetrahedron, 2010)
- Highly-efficient conversion of glycerol to solketal over heterogeneous Lewis acid catalysts (Green Chemistry, 2012)
- Glycerin Derivatives as Fuel Additives: The Addition of Glycerol/Acetone Ketal (Solketal) in Gasolines (Energy & Fuels, 2010)
- Low-temperature method for enhancement of enantioselectivity in the lipase-catalyzed kinetic resolutions of solketal and some chiral alcohols (Tetrahedron Letters, 1998)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2,2-dimethyl-1,3-dioxolane-4-methanol, (S)-isomer
- 2,2-dimethyl-1,3-dioxolane-4-methanol, (R)-isomer
- 2,2-dimethyl-1,3-dioxolane-4-methanol, (DL)-isomer
- 2,3-O-isopropylideneglycerol
- 2,2-dimethyl-1,3-dioxolane-4-methanol
- 2,3-isopropylidene-sn-glycerol
- glycerol acetonide
- 2,2-dimethyl-1,3-dioxolane-4-methanol, monosodium salt
- 2,2-dimethyl-4-hydroxymethyl-1,3-dioxolane
-
SMILESCC1(OCC(O1)CO)C
-
InChIKeyRNVYQYLELCKWAN-UHFFFAOYSA-N
- Pubchem - Solketal
- Wikipedia - solketal
Solketal is a protected form of glycerol with an isopropylidene acetal group joining two neighboring hydroxyl groups. Solketal contains a chiral center on the center carbon of the glycerol backbone, and so can be purchased as either the racemate or as one of the two enantiomers. Solketal has been used extensively in the synthesis of mono-, di- and triglycerides by ester bond formation.
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Similar Compounds
5464-28-8
(5464-28-8)
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2,2-Dimethyl-1,3-dioxolane-4-carbaldehyde
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(29908-11-0)
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(7476-20-2)
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ethyl 2-(2-methyl-1,3-dioxolan-2-yl)acetate
(6413-10-1)
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(4437-85-8)
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(4016-11-9)
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NSC623655
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Solketal
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