1036260-18-0

Basic information

• Product Name: (1S,3R)-3-Aminocyclopentanol
• Synonyms: (1S,3R)-3-Aminocyclopentanol;Cyclopentanol,3-amino-,(1S,3R)-;(1S,3R)-3-Aminocyclopentanol(WX600013)
• CAS NO: 1036260-18-0
• Molecular Formula: C₅H₁₁NO
• Molecular Weight: 101
• Mol File: 1036260-18-0.mol

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: (1S,3R)-3-Aminocyclopentanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,3R)-3-Aminocyclopentanol(1036260-18-0)
• EPA Substance Registry System: (1S,3R)-3-Aminocyclopentanol(1036260-18-0)

Safety Data

• Hazardous Substances Data: 1036260-18-0(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
(1S,3R)-3-Aminocyclopentanol is used as a key intermediate in the synthesis of complex organic molecules. Its unique stereochemistry allows for the creation of specific structural arrangements that are not possible with other isomers, making it a valuable component in the development of novel compounds.
Used in Pharmaceutical Production:
(1S,3R)-3-Aminocyclopentanol is used as a building block in the production of certain pharmaceuticals. Its presence in the molecular structure can influence the drug's activity, selectivity, and overall effectiveness, contributing to the development of new therapeutic agents.
Used in Research and Development:
(1S,3R)-3-Aminocyclopentanol is employed in research settings to study the effects of stereochemistry on molecular interactions and reactivity. Understanding these properties can lead to the discovery of new reaction pathways and the design of more efficient synthetic methods.
Safety Considerations:
The properties and effects of (1S,3R)-3-Aminocyclopentanol largely depend on specific conditions and concentrations. As with any chemical, it is essential to consider the potential hazards and take appropriate safety measures when handling and using this compound in various applications.

Upstream product

• 167298-58-0 (±)-cis-3-aminocyclopentanol 

Downstream Products

• 225641-84-9 tert-butyl N-[(1R,3S)-3-hydroxycyclopentyl]carbamate 
• 124555-33-5 (1S,3R)-3-aminocyclopentan-1-ol hydrochloride 
• 1616340-96-5 C₂₂H₂₁F₂N₃O₅ 
• 1656286-82-6 C₂₄H₂₃F₂N₃O₅ 
• 1616342-22-3 C₂₃H₂₄FN₃O₅ 
• 1616339-88-8 (2S,5R,13aS)-N-((S)-(4-fluorophenyl)ethyl)-8-hydroxy-7,9-dioxo-2,3,4,5,7,9,13,13a-octahydro-2,5-methanopyrido[1',2':4,5]pyrazino[2.1-b][1,3]oxazepine-10-carboxamide 
• 1616339-78-6 (2S,5R,13aS)-N-((R)-1-(2,4-difluorophenyl)ethyl)-8-hydroxy-7,9-dioxo-2,3,4,5,7,9,13,13a-octaliydro-2,5-methanopyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazepine-10-carboxamide 
• 1263371-46-5 (1S,3R)-3-(5'-chloro-6-(3-fluorobenzylamino)-2,4'-bipyridin-2'-yl-amino)cyclopentanol 

Relevant articles and documents

Preparation method of optically pure cyclic amino alcohol and salt thereof

The invention relates to the field of chemical pharmacy, particularly to a preparation method of optically pure cyclic amino alcohol and a salt thereof. The method comprises 1) hydrolysis: hydrolyzinga compound (12) to obtain a compound (13), and 2) catalytic hydrogenation: carrying out catalytic hydrogenation on the compound (13) obtained in the hydrolysis step to obtain a compound (1).

Method for preparing single-configuration 3-aminocyclopentanol through chiral resolution

The invention relates to a method for preparing a single-configuration 3- aminocyclopentanol through chiral resolution. Specifically, the invention discloses a chiral splitting method of 3-aminocyclopentanol. The preparation method is simple to operate, a

2-Substituted-1H-benz(de)-isoquinoline-1,3-(2H)-diones

Compounds of the following formula STR1 wherein R1 and R2 are independently selected from hydrogen, halogen, lower alkyl, lower alkoxy, lower alkylthio, nitro, cyano, and trifluoromethyl, and R is selected from a triacetyl substituted pentose, pentose, a tetraacetyl substituted hexose, hexose, a hydroxy substituted cycloalkyl of 5 to 7 carbons, STR2 wherein n is 1 or 2 and R3 is hydrogen, an alkali metal or alkaline earth metal ion; are disclosed. These compounds possess useful anti-inflammatory activity.