CAS 2631-77-8

3,5-Diiodosalicylaldehyde

Description:

3,5-Diiodosalicylaldehyde is an organic compound characterized by the presence of two iodine atoms and an aldehyde functional group attached to a salicylic acid derivative. Its molecular structure features a benzene ring with hydroxyl (-OH) and aldehyde (-CHO) substituents, along with the two iodine atoms located at the 3 and 5 positions relative to the aldehyde group. This compound is typically a solid at room temperature and may exhibit a pale yellow to brown color. It is known for its reactivity, particularly in electrophilic aromatic substitution reactions due to the electron-withdrawing nature of the iodine substituents. Additionally, 3,5-Diiodosalicylaldehyde can participate in various chemical reactions, including condensation and complexation, making it useful in organic synthesis and as a potential precursor for other chemical compounds. Its iodine content also suggests potential applications in medicinal chemistry and materials science, particularly in the development of iodine-containing pharmaceuticals or functional materials. Safety precautions should be observed when handling this compound due to its potential toxicity and reactivity.

Formula: C₇H₄I₂O₂

InChI: InChI=1S/C7H4I2O2/c8-5-1-4(3-10)7(11)6(9)2-5/h1-3,11H

InChI key: InChIKey=MYWSBJKVOUZCIA-UHFFFAOYSA-N

SMILES: C(=O)C1=C(O)C(I)=CC(I)=C1

Synonyms:

• 2-Hydroxy-3,5-Diiodobenzaldehyde
• 3,5-Diiodo-2-hydroxybenzaldehyde
• 3,5-Diiodo-2-hydroxybenzaldehyde~2-Hydroxy-3,5-diiodobenzaldehyde
• 3,5-Iodosalicylaldehyde
• Benzaldehyde, 2-hydroxy-3,5-diiodo-
• Salicylaldehyde, 3,5-diiodo-
• 3,5-Diiodosalicylaldehyde

3,5-Diiodosalicylaldehyde

CAS: 2631-77-8

Formula: C₇H₄I₂O₂

Purity: >98.0%(GC)(T)

Color and Shape: White to Yellow to Green powder to crystal

Molecular weight: 373.92

Ref: 3B-D4848

3,5-Diiodosalicylaldehyde, 98+%

CAS: 2631-77-8

3,5-Diiodosalicylaldehyde is used to synthesize new Schiff bases, (2,4-diiodo-6-[(2-morpholin-4-yl-ethylimino)-methyl]-phenol and 2,4-diiodo-6-[(3-morpholin-4-yl-propylimino)-methyl]-phenol) and the new tridentate ligand, [(2-hydroxy-3,5-diiodo-benzylidene)-amino]-acetic acid (HDBA), 3-bromo-N?-(2-h

Formula: C₇H₄I₂O₂

Purity: 98+%

Color and Shape: Powder, Cream or pale yellow to yellow-green or yellow-brown

Molecular weight: 373.92

Ref: 02-L05783

Benzaldehyde, 2-hydroxy-3,5-diiodo-

CAS: 2631-77-8

Formula: C₇H₄I₂O₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 373.9144

Ref: IN-DA002SO4

3,5-Diiodo-2-hydroxybenzaldehyde

CAS: 2631-77-8

3,5-Diiodo-2-hydroxybenzaldehyde

Formula: C₇H₄I₂O₂

Purity: 98%

Color and Shape: cream (hint of yellow) powder

Molecular weight: 373.91g/mol

Ref: 54-OR8810

3,5-Diiodosalicylaldehyde

CAS: 2631-77-8

3,5-Diiodosalicylaldehyde is a chemical compound found in the mushroom E. cloacae. It has been used as a model system to study the enzymatic reaction of methylene transfer from active methylene to inactive methylene. FTIR spectroscopy was used to confirm this reaction and structural analysis revealed that 3,5-diiodosalicylaldehyde is an active methylene with a structure similar to coumarin derivatives. The crystal structure of 3,5-diiodosalicylaldehyde was determined by X-ray crystallography and it was found that the molecule adopts a monoclinic coordination geometry.

Formula: C₇H₄I₂O₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 373.91 g/mol

Ref: 3D-FD70973

2-Hydroxy-3,5-diiodobenzaldehyde

CAS: 2631-77-8

Formula: C₇H₄I₂O₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 373.916

Ref: 10-F336733