Benzodioxoles

Aromatic organic heterocyclic compounds that consist of a benzene containing the methylenedioxy functional group; methylenedioxy functional groups have two oxygen atoms connected to a methylene bridge.

Search Within Results

361 – 375 of 400 results

361

eMolecules S-2-9H-FLUOREN-9-YLM 5G

5000188510 S-2-9H-FLUOREN-9-YLM 5G

Pricing & Availability

362

eMolecules EMOLECULES INC

5000472679 S-2-9H-FLUOREN-9-YLM 1G

Pricing & Availability

363

eMolecules EMOLECULES INC

5000473780 1R 2R-2-9H-FLUOREN-9-Y 25MG

Pricing & Availability

364

eMolecules EMOLECULES INC

5000473781 1R 2R-2-9H-FLUOREN-9-Y 50MG

Pricing & Availability

365

eMolecules EMOLECULES INC

5000482668 S-2-9H-FLUOREN-9-YL 10G

Pricing & Availability

366

eMolecules EMOLECULES INC

5000483098 2 2-DIFLUORO-1 3-BENZODIOXO 5G

Pricing & Availability

367

eMolecules 2-Hydroxymethyl-1,4-benzodioxane | 3663-82-9 | MFCD00006822 | 1g

Combi-Blocks | 2-Hydroxymethyl-1,4-benzodioxane | 1g | 448006101 | SS-9039 | 97.000 | 3663-82-9 | MFCD00006822 | 166.176 | C9H10O3

If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link:
eMolecules Building Block Tool

Pricing & Availability

368

Chemical Diversity Labs Inc 4-(1,3-BENZODIOXOL-5-YLOXY)1G

[4-(1,3-BENZODIOXOL-5-YLOXY)PHENYL]AMINE, 117401-33-9, MFCD02663332

Pricing & Availability

369

Cambridge Isotope Laboratories N-(3-Amino-3-oxopropyl)-val-FTH (valine-13C5 99%) 100 ug/mL in acetonitrile H2O (1 1) 1 2 mL

N-(3-Amino-3-oxopropyl)-val-FTH (valine-13C5 99%) 100 ug/mL in acetonitrile H2O (1 1) 1 2 mL

Pricing & Availability

370

Medchemexpress LLC Piperonylic acid | 94-53-1 | 99.9% | 166.13 | 100 G

Piperonylic acid is a natural molecule that structurally mimics trans-cinnamic acid due to its methylenedioxy function. It acts as a selective, mechanism-based inactivator of trans-cinnamate 4-Hydroxylase. This compound possesses anticancer, antioxidant, and antibacterial properties.

Mimics the structure of trans-cinnamic acid.
Functions as a selective, mechanism-based inactivator of trans-cinnamate 4-Hydroxylase.
Exhibits anticancer, antioxidant, and antibacterial activities.
Promotes growth and survival of HaCaT cells.
Accelerates wound healing in mice.