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
• Article Data: 3

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

General Description

"(1S,3R)-3-Aminocyclopentanol" is a specific isomer of aminocyclopentanol, a type of cycloalcohol with an amino functional group. The "1S,3R" denotes the stereochemistry of the molecule, indicating the orientation of the hydroxyl (alcohol) and amino groups on the cyclopentane ring. This chemical, like other aminocyclopentanols, can be used in a variety of organic synthesis reactions and may serve as an intermediate in the production of some pharmaceuticals. In terms of safety, its properties and effects would largely depend on specific conditions and concentrations.

Upstream product

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

Downstream Products

• 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 
• 225641-84-9 tert-butyl N-[(1R,3S)-3-hydroxycyclopentyl]carbamate 

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).

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.