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1-AMINO-6-NITROINDAN is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62658-54-2

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62658-54-2 Usage

Type of Compound

Organic compound

Functional Groups

Amino group and nitro group

Applications

a. Synthesis of pharmaceuticals
b. Synthesis of other organic compounds

Field of Interest

a. Medicinal chemistry
b. Development of new materials

Potential Biological Activities

Studied for its properties that may be useful in various applications in the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 62658-54-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,5 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62658-54:
(7*6)+(6*2)+(5*6)+(4*5)+(3*8)+(2*5)+(1*4)=142
142 % 10 = 2
So 62658-54-2 is a valid CAS Registry Number.

62658-54-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-nitro-2,3-dihydro-1H-inden-1-amine

1.2 Other means of identification

Product number -
Other names 6-nitro-indan-1-ylamine

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:62658-54-2 SDS

62658-54-2Relevant academic research and scientific papers

Aryl sulfonamido indane inhibitors of the Kv1.5 ion channel

Gross, Michael F.,Beaudoin, Serge,McNaughton-Smith, Grant,Amato, George S.,Castle, Neil A.,Huang, Christine,Zou, Anruo,Yu, Weifeng

, p. 2849 - 2853 (2008/02/11)

A collection of aryl sulfonamido indanes based on the lead compound 1 was synthesized and evaluated for Kv1.5 inhibitory activity. Kv1.5 inhibitors have the potential to be atrium-selective agents for treatment of atrial fibrillation. (1R,2R)-1 has an IC50 of 0.033 μM against Kv1.5 and is selective against other cardiac ion channels, including hERG.

Diamino thiazoloindan derivatives and their use

-

Page/Page column 18, (2008/06/13)

The subject invention provides a compound having the structure: wherein Y is O, NR3R4 or NOR6; R3 is H, alkyl, aralkyl, alkynyl, trifluoroacetyl, t-butoxycarbonyl or an acyl group; R4 is H, alkyl, aralkyl, or alkynyl; R6 is H or C1-C4 alkyl; R1 and R2 are each independently H, alkyl, aralkyl, or alkynyl; the curved line drawn from S to the center of the phenyl ring and the straight line drawn from N to the center of the ring indicate that S and N are part of a 5 membered ring which shares two carbons with the phenyl ring; and the dashed line drawn from the carbon atom on the cyclopentyl ring to Y represents a bond when Y is O or NOR6 and is absent when Y is NR3R4, and wherein wherein X is H or O; and R5 is H, alkyl, trifluoroacetyl, t-butoxycarbonyl or an acyl group, or an enantiomer, or a tautomer, or a pharmaceutically acceptable salt thereof, a process for preparing the compounds and a method of treating Parknison''s disease, multiple sclerosis or depression with the compounds of the invention.

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