CAS 37441-29-5

5-Amino-2,4,6-triiodo-1,3-benzenedicarbonyl dichloride

Description:

5-Amino-2,4,6-triiodo-1,3-benzenedicarbonyl dichloride, with the CAS number 37441-29-5, is a chemical compound characterized by its complex structure featuring multiple iodine substituents and functional groups. This compound is a derivative of benzenedicarbonyl dichloride, where three iodine atoms are attached to the benzene ring, enhancing its reactivity and potential applications in various fields. The presence of the amino group contributes to its ability to participate in further chemical reactions, such as nucleophilic substitutions. The dichloride functional groups indicate that it can act as a chlorinating agent or be involved in acylation reactions. Due to its iodine content, this compound may exhibit unique properties, including increased density and potential applications in imaging or as a contrast agent in medical diagnostics. Additionally, the presence of halogens often influences the compound's solubility and stability in different solvents. Overall, 5-Amino-2,4,6-triiodo-1,3-benzenedicarbonyl dichloride is a notable compound in organic chemistry with potential utility in pharmaceuticals and materials science.

Formula: C₈H₂Cl₂I₃NO₂

InChI: InChI=1S/C8H2Cl2I3NO2/c9-7(15)1-3(11)2(8(10)16)5(13)6(14)4(1)12/h14H2

InChI key: InChIKey=FBJVWRITWDYUAC-UHFFFAOYSA-N

SMILES: C(Cl)(=O)C1=C(I)C(C(Cl)=O)=C(I)C(N)=C1I

Synonyms:

• 1,3-Benzenedicarbonyl dichloride, 5-amino-2,4,6-triiodo-
• 5-Amino-2,4,6- triiodisophthaloyl acid
• 5-Amino-2,4,6- triiodisophthaloyl acid dichloride
• 5-Amino-2,4,6-Triiodobenzene-1,3-Dicarbonyl Dichloride
• 5-Amino-2,4,6-Triiodoisophtalic Acid Dichloride
• 5-Amino-2,4,6-triiodo-1,3-benzenedicarbonyl dichloride
• 5-Amino-2,4,6-triiodo-1,3-benzenedicarboxylic acid dichloride
• 5-Amino-2,4,6-triiodobenzene-1,3-dicarbonyl chloride
• 5-Amino-2,4,6-triiodoisophthalic acid dichloride
• 5-Amino-2,4,6-triiodoisophthaloy dichloride
• 5-Amino-2,4,6-triiodoisophthaloyl chloride
• 5-Amino-2,4,6-triiodoisophthaloyl dichloride
• 5-Aminotriiodoisophthaloyl dichloride

5-Amino-2,4,6-triiodoisophthaloyl Dichloride

CAS: 37441-29-5

Formula: C₈H₂Cl₂I₃NO₂

Purity: >96.0%(GC)

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

Molecular weight: 595.72

Ref: 3B-A2854

5-Amino-2,4,6-triiodoisophthaloyl dichloride

CAS: 37441-29-5

Formula: C₈H₂Cl₂I₃NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 595.7264

Ref: IN-DA0079QV

5-Amino-2,4,6-triiodoisophthaloyl dichloride

CAS: 37441-29-5

5-Amino-2,4,6-triiodoisophthaloyl dichloride

Purity: 98%

Molecular weight: 595.73g/mol

Ref: 54-OR1063178

Iohexol EP Impurity L

CAS: 37441-29-5

Formula: C₈H₂Cl₂I₃NO₂

Color and Shape: Yellow Solid

Molecular weight: 595.72

Ref: 4Z-I-3719

5-Amino-2,4,6,-triiodoisophthaloyl dichloride

CAS: 37441-29-5

5-Amino-2,4,6,-triiodoisophthaloyl dichloride is a triiodinated compound that has been shown to bind to the receptor for asialoglycoprotein. It is used in the diagnosis of liver and kidney diseases. 5-Amino-2,4,6,-triiodoisophthaloyl dichloride is taken up by tissues and organs and causes damage to these tissues. The chloride ion binds to the molecule, making it more water soluble. The lactobionic acid residue is then cleaved off by an enzyme in the cell called beta-galactosidase. This leaves a molecule containing iodine which can be detected with a diagnostic technique such as X-ray crystallography or nuclear magnetic resonance spectroscopy.

Formula: C₈H₂Cl₂I₃NO₂

Purity: Min. 95%

Color and Shape: Slightly Yellow Powder

Molecular weight: 595.73 g/mol

Ref: 3D-FA05533

Iohexol EP Impurity L

CAS: 37441-29-5

Formula: C₈H₂Cl₂I₃NO₂

Molecular weight: 595.72

Ref: ST-EA-CP-I67011