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1H,1'H-3,3'-(1-pyridin-3-yl-ethane-1,1-diyl)-bis-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37707-64-5

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37707-64-5 Usage

Chemical Structure

A bis-indole derivative containing a pyridine group

Type of Compound

Synthetic chemical compound

Pharmacological Properties

Being studied for potential applications in medicine

Therapeutic Potential

Possible use as a therapeutic agent for various medical conditions

Cancer

YL-109 may have potential anti-cancer properties

Neurological Disorders

The compound may also be useful in treating certain neurological conditions

Research Interest

YL-109 has attracted attention from researchers due to its unique chemical structure and potential applications

Current Status

More research is needed to fully understand the mechanisms of action and potential applications of YL-109

Drug Development

YL-109 is a promising candidate for further investigation and potential development as a pharmaceutical agent

Check Digit Verification of cas no

The CAS Registry Mumber 37707-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,0 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 37707-64:
(7*3)+(6*7)+(5*7)+(4*0)+(3*7)+(2*6)+(1*4)=135
135 % 10 = 5
So 37707-64-5 is a valid CAS Registry Number.

37707-64-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[1-(1H-indol-3-yl)-1-pyridin-3-ylethyl]-1H-indole

1.2 Other means of identification

Product number -
Other names 1,1-Di-indol-3-yl-1-<3-pyridyl>-ethan

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:37707-64-5 SDS

37707-64-5Downstream Products

37707-64-5Relevant academic research and scientific papers

Synthesis of Novel Indolo-Spirocyclic Compounds

El-Sayed, Mardia T.,Mahmoud, Kazem,Hilgeroth, Andreas,Fakhr, Issa M. I.

, p. 188 - 196 (2016)

(Chemical Equation Presented) In the present work, we succeeded to synthesize the novel indolo-spirocyclic compounds (4, 5, 6, 7 and 11) via electrophilic condensation reactions of indoles with carbonyl compounds including different types of ketones, for

Synthesis, anti-methicillin-resistant S. aureus (MRSA) evaluation, quantitative structure-activity relationship and molecular modeling studies of some novel bis-indoles as prospective MRSA pyruvate kinase

El Sayed, Inhibitors Mardia T.,Sabry, Nermien M.,Hamdy, Nehal A.,Voronkov, Andrey,Ogungbe, Ifedayo V.,Balakin, Konstantin,Abdel-Aziz, Mohamed S.

, p. 336 - 346 (2018/04/20)

Background: MRSA is a gram positive pathogen resistant to methicillin and other betalactam antibiotics, including penicillin, oxacillin, and declooxacillin. Statistical data suggest that as many as 19,000 people per year die from MRSA in the USA. Methods:

Silica-supported LiHSO4 as a highly efficient, mild, heterogeneous, and reusable catalytic system for the solvent-free synthesis of bis(indolyl)methanes

Hasaninejad, Alireza,Zare, Abdolkarim,Sharghi, Hashem,Khalifeh, Reza,Shekouhy, Mohsen

experimental part, p. 2508 - 2515 (2010/04/26)

Silica-supported LiHSO4 (LiHSO4/SiO2) is used as a green, cheap, and efficient catalytic system for the synthesis of bis(indolyl)methanes via the condensation of indoles with carbonyl compounds under solvent-free condition

Trityl chloride as a novel and efficient organic catalyst for room temperature preparation of bis(indolyl)methanes under solvent-free conditions in neutral media

Khalafi-Nezhad,Parhami,Zare,Moosavi Zare,Hasaninejad,Panahi

, p. 617 - 621 (2008/12/21)

A simple, clean, and highly efficient solvent-free procedure for the preparation of bis(1H-indol-3-yl)methanes is described from the reaction of carbonyl compounds (aldehydes and ketones) with 1H-indole in the presence of trityl chloride as a catalyst. Th

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