CAS 76820-34-3
:N1,N3-Bis(2,3-dihydroxypropyl)-5-nitro-1,3-benzenedicarboxamide
Description:
N1,N3-Bis(2,3-dihydroxypropyl)-5-nitro-1,3-benzenedicarboxamide, identified by its CAS number 76820-34-3, is a synthetic organic compound characterized by its complex molecular structure, which includes two hydroxyl groups and a nitro group attached to a benzene ring. This compound features a bis-amide functional group, indicating the presence of two amide linkages, which contribute to its potential solubility in polar solvents. The dihydroxypropyl substituents enhance its hydrophilicity, making it more soluble in aqueous environments. The nitro group introduces electron-withdrawing characteristics, which can influence the compound's reactivity and stability. This substance may exhibit biological activity, making it of interest in pharmaceutical and biochemical research. Its specific applications and interactions would depend on further studies, including its behavior in various chemical environments and its potential effects on biological systems. As with many chemical substances, safety data and handling precautions should be reviewed before use, given the presence of functional groups that may pose hazards.
Formula:C14H19N3O8
InChI:InChI=1S/C14H19N3O8/c18-6-11(20)4-15-13(22)8-1-9(3-10(2-8)17(24)25)14(23)16-5-12(21)7-19/h1-3,11-12,18-21H,4-7H2,(H,15,22)(H,16,23)
InChI key:InChIKey=LJEBHEAPZMNBSI-UHFFFAOYSA-N
SMILES:C(NCC(CO)O)(=O)C1=CC(C(NCC(CO)O)=O)=CC(N(=O)=O)=C1
Synonyms:- 1,3-Benzenedicarboxamide, N,N′-bis(2,3-dihydroxypropyl)-5-nitro-
- 1,3-Benzenedicarboxamide, N<sup>1</sup>,N<sup>3</sup>-bis(2,3-dihydroxypropyl)-5-nitro-
- 1-N,3-N-Bis(2,3-dihydroxypropyl)-5-nitrobenzene-1,3-dicarboxamide
- N,N'-bis(2,3-dihydroxypropyl)-5-nitrobenzene-1,3-dicarboxamide
- N1,N3-Bis(2,3-dihydroxypropyl)-5-nitroisophthalamide
- N<sup>1</sup>,N<sup>3</sup>-Bis(2,3-dihydroxypropyl)-5-nitro-1,3-benzenedicarboxamide
- 1,3-Benzenedicarboxamide, N1,N3-bis(2,3-dihydroxypropyl)-5-nitro-
- N1,N3-Bis(2,3-dihydroxypropyl)-5-nitro-1,3-benzenedicarboxamide
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Found 9 products.
Iohexol Related Compound C (N,N'-Bis(2,3-dihydroxypropyl)-5-nitro-1,3- benzenedicarboxamide)
CAS:Aromatic cyclic amides (including cyclic carbamates) and their derivatives; salts thereofFormula:C14H19N3O8Color and Shape:White PowderMolecular weight:357.11721N1,N3-bis(2,3-dihydroxypropyl)-5-nitroisophthalamide
CAS:Formula:C14H19N3O8Purity:98%Color and Shape:SolidMolecular weight:357.3160N1,N3-bis(2,3-dihydroxypropyl)-5-nitroisophthalamide
CAS:N1,N3-bis(2,3-dihydroxypropyl)-5-nitroisophthalamidePurity:98%N,N'-Bis(2,3-dihydroxypropyl)-5-nitro-1,3-benzenedicarboxamide
CAS:Controlled ProductFormula:C14H19N3O8Color and Shape:NeatMolecular weight:357.32N,N’-Bis(2,3-dihydroxypropyl)-5-nitro-1,3-benzenedicarboxamide
CAS:Controlled Product<p>Impurity Iohexol USP Related Compound C<br>Applications N,N'-Bis(2,3-dihydroxypropyl)-5-nitro-1,3-benzenedicarboxamide is used in the preparation of X-ray contrast agents.<br>References Haavaldsen, J. et al.: Acta Pharmac. Sue., 20, 219 (1983);<br></p>Formula:C14H19N3O8Color and Shape:White To Off-WhiteMolecular weight:357.32N,N’-BIS(2,3-DIHYDROXYPROPYL)-5-NITRO-1,3-BENZENEDICARBOXAMIDE
CAS:Purity:98%Molecular weight:357.3190002Iohexol impurity C
CAS:<p>Iohexol impurity C is a non-ionic organic compound that can be used as a reaction intermediate for the preparation of amidated iodinated x-ray contrast media. The amidation reaction is typically carried out in aqueous solution with an acid catalyst at room temperature for up to 24 hours. The amidation reaction condition and time can be optimized depending on the desired end product. Industrial preparation of iohexol typically involves the use of an x-ray generator and iopamidol, which is synthesized from diethylene triamine and ethylenediamine. Iohexol is marketed under the trade name Omnipaque, which contains iohexol impurity C as one of its components.</p>Formula:C14H19N3O8Purity:Min. 95%Molecular weight:357.32 g/mol








