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8-methyl-8-azabicyclo[3.2.1]oct-3-yl 1H-indole-3-carboxylate is a complex organic compound with a molecular formula of C16H20N2O2. It is characterized by a bicyclic structure, with an 8-azabicyclo[3.2.1]octane ring fused to an indole-3-carboxylate group. The compound features a methyl group at the 8-position of the azabicyclo ring and a carboxylate group attached to the indole moiety. This chemical is known for its potential applications in medicinal chemistry, particularly in the development of drugs targeting the serotonin receptor, due to its structural similarity to certain psychoactive substances. Its synthesis and biological activity are of interest to researchers in the field of drug discovery and development.

156-45-6

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156-45-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156-45-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,5 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 156-45:
(5*1)+(4*5)+(3*6)+(2*4)+(1*5)=56
56 % 10 = 6
So 156-45-6 is a valid CAS Registry Number.

156-45-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-Methyl-8-azabicyclo[3.2.1]oct-3-yl 1H-indole-3-carboxylate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:156-45-6 SDS

156-45-6Downstream Products

156-45-6Relevant academic research and scientific papers

Antibacterial action of (5-nitrofurfuryl)-derived aminophosphonates and their parent imines

Lewkowski, Jaros?aw,Morawska, Marta,Kowalczyk, Aleksandra

, p. 365 - 374 (2019)

Abstract: Ten aminophosphonates bearing 2-nitrofuran moiety and two N-aryl 5-nitro-furfuralaldimines, namely, N-(2-nitrofurfurylidene)-p-toluidine and N-(2-nitrofurfurylidene)-p-anisidine, were tested in aspect of their antibacterial action. O,O′-diphenyl

SOME DATA ON THE CHEMISTRY OF 5-NITRO-2-FURALDEHYDE, V. ANILINE DERIVATIVES

Csaszar, Jozsef

, p. 245 - 258 (2007/10/02)

UV, IR and 1H-NMR spectra of Schiff bases of 5-nitro-2-furaldehyde with mono- and disubstituted anilines have been investigated.The spectra measured in methanol, in acidic and basic media and in concentrated sulfuric acid are discussed in conne

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