CAS 22323-82-6

(S)-2,2-dimethyl-1,3-dioxolane-4-methanol

Description:

(S)-2,2-Dimethyl-1,3-dioxolane-4-methanol is a chemical compound characterized by its unique structure, which includes a dioxolane ring and a hydroxymethyl group. This compound is a chiral molecule, meaning it has non-superimposable mirror images, with the (S) designation indicating its specific stereochemistry. It typically appears as a colorless to pale yellow liquid and is soluble in polar solvents due to the presence of the hydroxyl group. The dioxolane ring contributes to its stability and reactivity, making it useful in various chemical syntheses and applications. Its properties may include moderate volatility and a relatively low boiling point, which are common for similar organic compounds. Additionally, it may exhibit interesting reactivity patterns, such as participating in nucleophilic substitutions or serving as a precursor in the synthesis of more complex molecules. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₆H₁₂O₃

InChI: InChI=1/C6H12O3/c1-6(2)8-4-5(3-7)9-6/h5,7H,3-4H2,1-2H3

InChI key: InChIKey=RNVYQYLELCKWAN-YFKPBYRVSA-N

SMILES: C(O)[C@@H]1OC(C)(C)OC1

Synonyms:

• ((4S)-2,2-Dimethyl-1,3-dioxolan-4-yl)methanol
• (+)-2,2-Dimethyl-1,3-dioxolane-4-methanol
• (+)-2,3-O-Isopropylidene-sn-glycerol
• (+)-Glycerol acetonide
• (+)-Solketal
• (+)-α,β-Isopropylideneglycerol
• (2S)-Glycerol 1,2-acetonide
• (4S)-2,2-Dimethyl-1,3-dioxolan-4-ylmethanol
• (4S)-2,2-Dimethyl-1,3-dioxolane-4-methanol
• (S)-(+)-1,2-Isopropylideneglycerol
• (S)-(+)-1,2-O-Isopropylideneglycerol
• (S)-(+)-2,2-Dimethyl-1,3-dioxolan-4-methanol
• (S)-(+)-2,2-Dimethyl-4-hydroxymethyl-1,3-Dioxolane
• (S)-(+)-Solketal
• (S)-2,2-Dimethyl4-hydroxymethyl-1,3-Dioxolane
• (S)-2,3-Isopropylidene Glycerol
• (S)-Glycerol Acetonide
• (S)-Isopropylideneglycerol
• 1,2-Isopropylidene-SN-Glycerol
• 1,2-O-Isopropylidene-(S)-glycerol
• 1,2-O-Isopropylidene-SN-Glycerol
• 1,3-Dioxolane-4-methanol, 2,2-dimethyl-, (4S)-
• 1,3-Dioxolane-4-methanol, 2,2-dimethyl-, (S)-
• 1,3-Dioxolane-4-methanol, 2,2-dimethyl-, <span class="text-smallcaps">L</span>-
• 2,3-O-Isopropylidene-<span class="text-smallcaps">D</span>-glycerol
• <span class="text-smallcaps">L</span>-(+)-2,2-Dimethyl-1,3-dioxolane-4-methanol
• D-(+)-1,2-Isopropylideneglycerol
• D-1,2-O-Isopropylidene-SN-Glycerol
• D-ALPHA,BETA-Isopropylideneglycerol
• D-Glycerol-acetonide
• Isopropylideneglycerol (S)-(+)-1,2-O-
• S-(+)-(2,2-Dimethyl-[1,3]dioxolan-4-YL)-methanol
• S-(-)-2,3-O-Isopropylideneglycerol
• S-Glycerol
• (S)-(+)-2,2'-Dimethyl-1,3-dioxolane-4-methanol
• 1,3-Dioxolane-4-methanol, 2,2-dimethyl-, L-
• (S)-(+)-2,2-Dimethyl-1,3-dioxolane-4-methanol
• S(+)-2,2'-dimethyl-1,3-dioxolane-4-methanol
• L-(+)-2,2-Dimethyl-1,3-dioxolane-4-methanol

(S)-(+)-2,2-Dimethyl-1,3-dioxolane-4-methanol

CAS: 22323-82-6

Formula: C₆H₁₂O₃

Purity: >98.0%(GC)

Color and Shape: Colorless to Light yellow clear liquid

Molecular weight: 132.16

Ref: 3B-D1691

(S)-(+)-2,3-O-Isopropylideneglycerol, 98%

CAS: 22323-82-6

(S)-(+)-2,3-O-Isopropylideneglycerol acts as a MEK inhibitor with antitumor activity. It is also employed in the preparation of a chiral allylic triol through extrusion of sulfur dioxide from an alfa,beta-epoxysulfone. This Thermo Scientific Chemicals brand product was originally part of the Alfa Ae

Formula: C₆H₁₂O₃

Purity: 98%

Color and Shape: Clear colorless to pale yellow, Liquid

Molecular weight: 132.16

Ref: 02-B24488

(S)-(+)-2,2-Dimethyl-1,3-dioxolane-4-methanol

CAS: 22323-82-6

Formula: C₆H₁₂O₃

Purity: 96%

Color and Shape: Liquid

Molecular weight: 132.1577

Ref: IN-DA0032FZ

(4S)-(+)-2,2-Dimethyl-4-(hydroxymethyl)-1,3-dioxolane

CAS: 22323-82-6

(4S)-(+)-2,2-Dimethyl-4-(hydroxymethyl)-1,3-dioxolane

Formula: C₆H₁₂O₃

Purity: 98%

Color and Shape: clear. colourless liquid

Molecular weight: 132.16g/mol

Ref: 54-OR40067

(+)-Solketal

CAS: 22323-82-6

(+)-Solketal is a product of glycerol acetalisation and is widely used in research and experiments in the field of life sciences.

Formula: C₆H₁₂O₃

Color and Shape: Solid

Molecular weight: 132.16

Ref: TM-TYD-00297

(S)-(+)-2,2-Dimethyl-1,3-dioxolane-4-methanol

Controlled Product

CAS: 22323-82-6

Applications A MEK inhibitor with antitumor activity.
References Lee, W., et al.: Bioorg. Med. Chem. Lett., 15, 3573 (2005), Normanno, N., et al.: J. Cell. Physiology, 207, 420 (2006), Narlawar, R., et al.: J. Med. Chem., 49, 7588 (2006),

Formula: C₆H₁₂O₃

Color and Shape: Neat

Molecular weight: 132.16

Ref: TR-D472635

1,2-O-Isopropylidene-sn-glycerol

CAS: 22323-82-6

1,2-O-Isopropylidene-sn-glycerol is a versatile building block that can be used in the synthesis of complex compounds. It is a useful scaffold for the construction of new molecules and has been used in the synthesis of several drugs. 1,2-O-Isopropylidene-sn-glycerol is also a reagent for organic synthesis and has been found to have high quality. CAS No. 22323-82-6

Formula: C₆H₁₂O₃

Molecular weight: 132.16 g/mol

Ref: 3D-I-8360

(S)-(+)-2,2-Dimethyl-1,3-dioxolane-4-methanol

CAS: 22323-82-6

Formula: C₆H₁₂O₃

Purity: 96%

Color and Shape: Liquid, Clear

Molecular weight: 132.159

Ref: 10-F024785

1,2-O-Isopropylidene-sn-glycerol

CAS: 22323-82-6

1,2-O-Isopropylidene-sn-glycerol (1,2-OIPG) is a synthetic molecule. It is synthesized from potassium thioacetate and chloride in an organic solvent with hexadecyl methanesulfonate as the catalyst. The product is obtained by intramolecular hydrogenation of the glyceride to produce 1,2-OIPG. This compound has been used as a strategy to generate hydrogen bonds in asymmetric synthesis, for example in the formation of d-mannitol with activated hydrogen bonds. The compound also has potential applications in the production of fatty acids.

Formula: C₆H₁₂O₃

Purity: Min. 98 Area-%

Color and Shape: Colorless Clear Liquid

Molecular weight: 132.15 g/mol

Ref: 3D-FI07166