785039-57-8

Basic information

• Product Name: 1,2-Cyclopentanediol,4-amino-3-(hydroxymethyl)-5-methoxy-,(1R,2R,3R,4S,5R)-rel-(9CI)
• Synonyms: 1,2-Cyclopentanediol,4-amino-3-(hydroxymethyl)-5-methoxy-,(1R,2R,3R,4S,5R)-rel-(9CI)
• CAS NO: 785039-57-8
• Molecular Formula: C7H15NO4
• Molecular Weight: 177.1983
• Product Categories: METHOXY
• Mol File: 785039-57-8.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2-Cyclopentanediol,4-amino-3-(hydroxymethyl)-5-methoxy-,(1R,2R,3R,4S,5R)-rel-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Cyclopentanediol,4-amino-3-(hydroxymethyl)-5-methoxy-,(1R,2R,3R,4S,5R)-rel-(9CI)(785039-57-8)
• EPA Substance Registry System: 1,2-Cyclopentanediol,4-amino-3-(hydroxymethyl)-5-methoxy-,(1R,2R,3R,4S,5R)-rel-(9CI)(785039-57-8)

Safety Data

• Hazardous Substances Data: 785039-57-8(Hazardous Substances Data)

Usage

Chemical classification

Amino alcohol
It contains both an amino group (-NH2) and hydroxyl groups (-OH), making it an amino alcohol.

Derivative

Cyclopentane
The compound is derived from cyclopentane, a five-membered ring with five carbon atoms.

Hydroxymethyl and methoxy groups

Present
The compound contains a hydroxymethyl (-CH2OH) group and a methoxy (-OCH3) group, which contribute to its reactivity and properties.

Stereochemistry

(1R,2R,3R,4S,5R)-rel-(9CI)
The compound has a specific stereochemistry, with the (1R,2R,3R,4S,5R) configuration, which defines the spatial arrangement of its atoms.

Application

Organic synthesis and drug research
It is used as a building block for creating complex molecules in organic synthesis and drug research.

Potential reactivity

Hydroxymethyl group
The hydroxymethyl group may serve as a potential source of reactivity for chemical reactions, allowing for further functionalization and modification.

Further research

Required
More research and testing are needed to fully understand the properties and potential applications of this compound.