CAS 29668-44-8

1,4-Benzodioxan-6-carboxaldehyde

Description:

1,4-Benzodioxan-6-carboxaldehyde, with the CAS number 29668-44-8, is an organic compound characterized by its bicyclic structure, which includes a benzene ring fused to a dioxane ring. This compound features a carboxaldehyde functional group (-CHO) at the 6-position of the dioxan ring, contributing to its reactivity and potential applications in organic synthesis. It is typically a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. The presence of the aldehyde group makes it susceptible to oxidation and nucleophilic attack, allowing it to participate in various chemical reactions, such as condensation and addition reactions. Additionally, 1,4-benzodioxan derivatives are of interest in medicinal chemistry and materials science due to their unique structural properties. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if inhaled or ingested. Proper storage and handling protocols are essential to ensure safety in laboratory environments.

Formula: C₉H₈O₃

InChI: InChI=1S/C9H8O3/c10-6-7-1-2-8-9(5-7)12-4-3-11-8/h1-2,5-6H,3-4H2

InChI key: InChIKey=CWKXDPPQCVWXAG-UHFFFAOYSA-N

SMILES: C(=O)C=1C=C2C(=CC1)OCCO2

Synonyms:

• 1,4-Benzodioxan-7-formaldehyde
• 1,4-Benzodioxane-6-aldehyde
• 1,4-Benzodioxane-6-carboxaldehyde
• 1,4-Benzodioxin-6-carboxaldehyde
• 1,4-Benzodioxin-6-carboxaldehyde, 2,3-dihydro-
• 2,3-Dihydro-1,4-benzodioxan-6-carboxaldehyde
• 2,3-Dihydro-1,4-benzodioxin-6-aldehyde
• 2,3-Dihydro-1,4-benzodioxin-6-carboxaldehyde
• 2,3-Dihydro-1,4-benzodioxine-6-carbaldehyde
• 2,3-Dihydro-benzo[1,4]dioxine-6-carbaldehyde
• 2,3-Dihydrobenzo[1,4]dioxine-6-carboxaldehyde
• 2,3-Dihydrobenzo[B][1,4]Dioxine-6-Carbaldehyde
• 2,3-Dihydrobenzo[b][1,4]dioxin-6-carboxaldehyde
• 2,3-Dihydrobenzo[b][1,4]dioxine-6-carboxaldehyde
• 3,4-Ethylenedioxybenzaldehyde
• 4H-1,3-benzodioxine-6-carbaldehyde

1,4-Benzodioxane-6-carboxaldehyde, 99%

CAS: 29668-44-8

1,4-Benzodioxan-6-carboxaldehyde finds its uses as building block in the synthesis of tetrahydroisoquinolinones, in the preparation of benzofuran analog, a potential inhibitor of CAMP-specific phosphodiesterase type IV, in the synthesis of (5Z)-5-(2,3-dihydro-1,4-benzodioxan-6-ylmethylene)-1-methyl-

Formula: C₉H₈O₃

Purity: 99%

Color and Shape: Pale cream to pale brown, Crystals or powder or crystalline powder

Molecular weight: 164.16

Ref: 02-A18696

1,4-Benzodioxin-6-carboxaldehyde, 2,3-dihydro-

CAS: 29668-44-8

Formula: C₉H₈O₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 164.1580

Ref: IN-DA002Z1A

3,4-Ethylenedioxybenzaldehyde

CAS: 29668-44-8

Formula: C₉H₈O₃

Purity: >98.0%(GC)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 164.16

Ref: 3B-B2019

1,4-Benzodioxan-6-carboxaldehyde

CAS: 29668-44-8

1,4-Benzodioxan-6-carboxaldehyde

Purity: 98%

Molecular weight: 164.16g/mol

Ref: 54-OR9850

3,4-Ethylenedioxybenzaldehyde

CAS: 29668-44-8

Intermediate in the synthesis of eliglustat

Formula: C₉H₈O₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 164.16 g/mol

Ref: 3D-FE59858

2,3-Dihydro-1,4-benzodioxine-6-carbaldehyde

CAS: 29668-44-8

Formula: C₉H₈O₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 164.16

Ref: 10-F065323