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59108-53-1

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59108-53-1 Usage

General Description

CHROMAN-3-YLAMINE, also known as 1-amino-2,3-dihydro-1H-indene, is a chemical compound with the molecular formula C9H11NO. It belongs to the class of organic compounds known as chromanes, which are a group of compounds containing a chromane moiety, which consists of a benzene ring fused to an oxygen-containing six-membered aliphatic ring. CHROMAN-3-YLAMINE is commonly used as a building block in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It has also been studied for its potential pharmacological properties, including as an anti-inflammatory and antioxidant agent. Additionally, CHROMAN-3-YLAMINE has been investigated for its potential role in treating neurodegenerative diseases such as Parkinson's and Alzheimer's.

Check Digit Verification of cas no

The CAS Registry Mumber 59108-53-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,0 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 59108-53:
(7*5)+(6*9)+(5*1)+(4*0)+(3*8)+(2*5)+(1*3)=131
131 % 10 = 1
So 59108-53-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO/c10-8-5-7-3-1-2-4-9(7)11-6-8/h1-4,8H,5-6,10H2/t8-/m1/s1

59108-53-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-Chroman-3-amine hydrochloride

1.2 Other means of identification

Product number -
Other names (3R)-3,4-dihydro-2H-chromen-3-amine,hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:59108-53-1 SDS

59108-53-1Upstream product

59108-53-1Downstream Products

59108-53-1Relevant articles and documents

Asymmetric amination of tetralone and chromanone derivatives employing ω-transaminases

Pressnitz, Desiree,Fuchs, Christine S.,Sattler, Johann H.,Knaus, Tanja,Macheroux, Peter,Mutti, Francesco G.,Kroutil, Wolfgang

, p. 555 - 559 (2013)

Various (S)-selective and (R)-selective ω-transaminases were investigated for the amination of 1- and 2-tetralone and derivatives as well as of 3- and 4-chromanone. All ketones tested were aminated to give the corresponding enantiopure amines (ee > 99%) employing at least one of the enzymes investigated. In most of the cases the (S)- as well as the (R)-enantiomer was obtained in optically pure form. The amination of 3-chromanone was performed on a 100 mg scale leading to optically pure (R)-3-aminochromane (ee > 99%) with complete conversion and 78% isolated yield.

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