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1H-Indol-5-amine,2,3-dihydro-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15918-80-6

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15918-80-6 Usage

Derivative of

Indole

Usage

Synthesis of drugs and medications (psychoactive and antidepressant properties), building block for synthesis of other complex molecules in organic chemistry research

Fields of application

Medicine, chemistry

Versatility

Wide range of potential applications

Check Digit Verification of cas no

The CAS Registry Mumber 15918-80-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,1 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15918-80:
(7*1)+(6*5)+(5*9)+(4*1)+(3*8)+(2*8)+(1*0)=126
126 % 10 = 6
So 15918-80-6 is a valid CAS Registry Number.

15918-80-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-amino indoline

1.2 Other means of identification

Product number -
Other names 5-aminoindoline

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:15918-80-6 SDS

15918-80-6Relevant academic research and scientific papers

Bicyclic oxazolidinones as antibacterial agents

-

, (2008/06/13)

The present invention provides compounds of formula I useful as antimicrobial agents wherein W, X, Y, R1, R2 and n are as defined in thereof.

N-GLUCOSYLATION OF AMINOINDOLINES AND THE BISGLUCOSIDES OF 5-AMINOINDOLE

Salekh, M. A.,Krasavina, L. S.,Vigdorchik, M. M.,Turchin, K. F.,Sapukova, A. A.,et al.

, p. 2348 - 2355 (2007/10/02)

The reaction of 1-acetyl-5- and 1-acetyl-6-aminoindolines with D-glucose gave the N-β-D-glucopyranosides of 1-acetyl-5- and 1-acetyl-6-aminoindolines, the β-configurations of which were preserved during conversion into the O-acetylated derivatives.The reaction of D-glucose with 5-aminoindoline followed by O-acetylation gave the O-acetylated bis-N1,N5-glucopyranoside of 5-aminoindoline as a mixture of the 1β,5β and 1β,5α anomers.Dehydrogenation followed by O-deacetylation led to the bis-N1,N5-glucopyranoside of 5-aminoindole also as a mixture of the 1β,5β and 1β,5α anomers.During the N-acetylation of the O-acetylated bis-N1,N5-glucoside of 5-aminoindoline the corresponding 5-acetamide derivative was obtained in the form of the individual 1β,5β anomer, which was converted after dehydrogenation and O-deacetylation into the individual 1β,5β anomer of the bis-N1,N5-glucopyranoside of 5-acetamidoindole.

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