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Benzamide, N-[2-(2,2-di-1H-indol-3-ylethyl)-phenyl]- is a complex organic compound with the chemical formula C26H22N2O. It is a derivative of benzamide, featuring a phenyl group connected to a benzamide moiety through an ethyl bridge. The ethyl bridge is substituted with two indole rings, each containing a nitrogen atom. Benzamide,N-[2-(2,2-di-1H-indol-3-ylethyl)- phenyl]- is known for its potential applications in pharmaceutical research, particularly in the development of drugs targeting the serotonin receptor system. Its structure allows it to interact with biological targets, making it a subject of interest for scientists exploring new therapeutic avenues.

52831-33-1

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52831-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52831-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,3 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52831-33:
(7*5)+(6*2)+(5*8)+(4*3)+(3*1)+(2*3)+(1*3)=111
111 % 10 = 1
So 52831-33-1 is a valid CAS Registry Number.

52831-33-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-7-dimethylamino-phenothiazinylium betaine

1.2 Other means of identification

Product number -
Other names N.N-Dimethyl-thionin

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:52831-33-1 SDS

52831-33-1Downstream Products

52831-33-1Relevant academic research and scientific papers

NAPHTHYRIDES IN HETARYLATION REACTIONS

Sheinkman, A. K.,Nezdiiminoga, T. N.,Chmilenko, T. S.,Klyuev, N. A.

, p. 986 - 990 (2007/10/02)

The reaction of indole (2-methylindole) with 1,5-, 1,6-, and 1,8-naphthyridines at 20 deg C, in the presence of benzoyl chloride, leads to the preferential formation of dihydro structures with one indolyl substituent at the α-position to the hetero atom.W

Reactions entre l'indole et les chlorures d'acides, en milieu basique: Synthese d'amides de l'ortho -2 ethyl, aniline

Bourgeois, Paul,Mesdouze, Jean,Philogene, Emile

, p. 1043 - 1046 (2007/10/02)

Acid chlorides react with indole in alkaline aqueous medium and yield amides of o-aniline which is in fact a trimer of indole.Their formation can be understood as follows: autocondensation of indole to give 2,3-diindole; acylatio

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