72704-51-9

Basic information

• Product Name: (2R,3R,4R,5S)-6-methylaminohexane-1,2,3,4,5-pentol
• Synonyms: 3-[[2-[2-[2-[(3-carboxy-2,4,6-triiodo-phenyl)carbamoylmethoxy]ethoxy]ethoxy]acetyl]amino]-2,4,6-triiodo-benzoic acid;2-[2-[carboxylatomethyl-[2-(carboxylatomethyl-(carboxymethyl)amino)ethyl]amino]ethyl-(carboxymethyl)amino]acetate;gadolinium(+3) cation;iotroxic acid meglumine salt
• CAS NO: 72704-51-9
• Molecular Formula: C29H35I6N3O14
• Molecular Weight: 1411.07
• Mol File: 72704-51-9.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (2R,3R,4R,5S)-6-methylaminohexane-1,2,3,4,5-pentol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R,4R,5S)-6-methylaminohexane-1,2,3,4,5-pentol(72704-51-9)
• EPA Substance Registry System: (2R,3R,4R,5S)-6-methylaminohexane-1,2,3,4,5-pentol(72704-51-9)

Safety Data

• Hazardous Substances Data: 72704-51-9(Hazardous Substances Data)

Usage

Description

(2R,3R,4R,5S)-6-methylaminohexane-1,2,3,4,5-pentol is a complex organic chemical compound characterized by its unique molecular structure. It features a pentol functional group and a methylamino substituent, along with four chiral centers that contribute to its multiple stereoisomers. (2R,3R,4R,5S)-6-methylaminohexane-1,2,3,4,5-pentol holds potential for use in pharmaceuticals and as a building block for synthesizing other organic compounds, with its intricate structure and chiral nature making it a subject of interest for further study and application in various chemical processes.

Uses

Used in Pharmaceutical Industry:
(2R,3R,4R,5S)-6-methylaminohexane-1,2,3,4,5-pentol is used as a potential building block for the synthesis of pharmaceutical compounds due to its complex molecular structure and chiral nature. Its unique properties may contribute to the development of new drugs and therapeutic agents.
Used in Chemical Research:
In the field of chemical research, (2R,3R,4R,5S)-6-methylaminohexane-1,2,3,4,5-pentol serves as an intriguing molecule for study. Its multiple stereoisomers and chiral centers provide opportunities for exploring the effects of stereochemistry on chemical reactions and properties, which can lead to advancements in understanding and manipulating molecular structures for specific applications.