CAS 22323-80-4

(4S)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde

Description:

(4S)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde is a chemical compound characterized by its unique dioxolane ring structure, which contributes to its reactivity and potential applications in organic synthesis. This compound features a carboxaldehyde functional group, making it an aldehyde, which is known for its reactivity in nucleophilic addition reactions. The presence of two methyl groups at the 2-position of the dioxolane ring enhances its steric properties and can influence its chemical behavior, including its boiling point and solubility. The specific stereochemistry indicated by the (4S) designation suggests that the compound has a defined spatial arrangement, which can affect its interactions with biological systems and other chemical species. Typically, compounds like this may be utilized in the synthesis of more complex organic molecules, including pharmaceuticals and agrochemicals, due to their functional groups and structural features. Safety data and handling precautions should be considered, as with all chemical substances, to ensure proper laboratory practices.

Formula: C₆H₁₀O₃

InChI: InChI=1/C6H10O3/c1-6(2)8-4-5(3-7)9-6/h3,5H,4H2,1-2H3/t5-/m1/s1

InChI key: InChIKey=YSGPYVWACGYQDJ-RXMQYKEDSA-N

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

Synonyms:

• (4S)-2,2-Dimethyl-1,3-dioxolan-4-carboxaldehyde
• (4S)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde
• (4S)-2,2-dimethyl-1,3-dioxolane-4-carbaldehyde
• (S)-2,2-Dimethyl-1,3-Dioxolane-4-Carbaldehyde
• (S)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde
• (S)-2,3-(Isopropylidenedioxy)propionaldehyde
• (S)-2,3-O-Isopropylideneglyceraldehyde
• (S)-Glyceraldehyde Acetonide
• (S)-Glyceraldehyde isopropylidene acetal
• (S)-Isopropylideneglyceraldehyde
• 1,3-Dioxolane-4-carboxaldehyde 2,2-dimethyl-, (4S)-
• 1,3-Dioxolane-4-carboxaldehyde, 2,2-dimethyl-, (S)-
• 1,3-Dioxolane-4-carboxaldehyde, 2,2-dimethyl-, <span class="text-smallcaps">L</span>-
• 2,3-O-Isopropylidene-<span class="text-smallcaps">L</span>-glyceraldehyde
• <span class="text-smallcaps">L</span>-Glyceraldehyde acetonide
• 2,3-O-Isopropylidene-L-glyceraldehyde
• 1,3-Dioxolane-4-carboxaldehyde, 2,2-dimethyl-, L-
• 2,3-O-ISOPROPYLIDENE-L-GLYCERALDEHYDE ((S)-GLYCERALDEHYDE ACETONIDE)
• L-isopropylidene glyceraldehyde)
• S-2,3-O-isopropylidene-glyceraldehyde
• (S)-2,3-ISOPROPYLIDENE GLYCERALDEHYDE
• L-GLYCERALDEHYDE ACETONIDE

(S)-2,2-Dimethyl-1,3-dioxolane-4-carbaldehyde

CAS: 22323-80-4

Formula: C₆H₁₀O₃

Color and Shape: Liquid

Molecular weight: 130.1418

Ref: IN-DA0032GO

2,3-O-Isopropylidene-L-glyceraldehyde

CAS: 22323-80-4

Ref: 7W-GC5272

(S)-Glyceraldehyde acetonide, 50% DCM

CAS: 22323-80-4

(S)-Glyceraldehyde acetonide, 50% DCM

Formula: C₆H₁₀O₃

Purity: 97%

Color and Shape: clear. colourless liquid

Molecular weight: 130.14g/mol

Ref: 54-OR912490

Nintedanib Impurity 31

CAS: 22323-80-4

Formula: C₆H₁₀O₃

Molecular weight: 130.14

Ref: 4Z-N-066048

Nintedanib Impurity 111

CAS: 22323-80-4

Formula: C₆H₁₀O₃

Molecular weight: 130.14

Ref: ST-EA-CP-N24079

2,3-O-Isopropylidene-L-glyceraldehyde - 50% DCM solution

CAS: 22323-80-4

2,3-O-Isopropylidene-L-glyceraldehyde (2,3-OIPA) is a synthetic compound that was developed as an alternative to paraformaldehyde for the synthesis of enantiopure compounds. It has been used in metathesis reactions and catalysed the conversion of β-unsaturated ketones to enantiopure products. 2,3-OIPA also has significant cytotoxic activity against a range of human cancer cell lines. This compound can be used in asymmetric syntheses to produce chiral molecules with a high degree of optical purity.

Formula: C₆H₁₀O₃

Purity: Min. 95%

Color and Shape: Colorless Powder

Molecular weight: 130.14 g/mol

Ref: 3D-MI13896