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16571-53-2

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16571-53-2 Usage

Indole derivative

A derivative of the indole structure This compound is based on the indole framework, which is a common structural motif in many biologically active molecules.

Methyl group

A CH3 functional group The presence of a methyl group (a carbon atom bonded to three hydrogen atoms) may influence the compound's properties and reactivity.

Pyridine ring

Contains a six-membered nitrogen-containing aromatic ring The pyridine ring is an essential part of the compound's structure and contributes to its biological activity.

Ethyl group

A C2H5 functional group The ethyl group (two carbon atoms connected to three hydrogen atoms) is another functional group present in the compound, which can affect its properties and reactivity.

Organic chemistry and pharmaceutical applications

Utilized in the fields of organic chemistry and pharmaceuticals This compound is relevant in the synthesis and development of new organic compounds and drugs.

Potential drug development

Involved in drug development and research 1-methyl-3-[2-(4-pyridyl)ethyl]-1H-indole may be used as a starting point or building block for the development of new drugs.

Biological activities

Exhibits diverse biological activities The compound has been found to possess various biological activities, such as anti-inflammatory and analgesic properties.

Therapeutic potential

Studied for its potential therapeutic effects on various diseases and conditions Researchers are interested in the potential use of this compound in treating different diseases and medical conditions.

Importance in medical research

An important molecule in medical research and development 1-methyl-3-[2-(4-pyridyl)ethyl]-1H-indole is a significant compound due to its potential applications in drug development and understanding its biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 16571-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,7 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16571-53:
(7*1)+(6*6)+(5*5)+(4*7)+(3*1)+(2*5)+(1*3)=112
112 % 10 = 2
So 16571-53-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H16N2/c1-18-12-14(15-4-2-3-5-16(15)18)7-6-13-8-10-17-11-9-13/h2-5,8-12H,6-7H2,1H3

16571-53-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-3-(2-pyridin-4-ylethyl)indole

1.2 Other means of identification

Product number -
Other names 1-methyl-3-(2-(4-pyridyl)ethyl)indole

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:16571-53-2 SDS

16571-53-2Relevant articles and documents

PHARMACEUTICAL COMPOUNDS

-

Page/Page column 34-35, (2010/02/07)

The invention provides a compound for use in the prophylaxis or treatment of a disease state or condition mediated by a p38 MAP kinase such as rheumatoid arthritis and osteoarthritis; the compound being of the general formula (I): wherein U, T, V and W are each a nitrogen atom or a group CR4 provided that no more than three of U, T, V and W are nitrogen atoms; R0 is hydrogen, C1-4 hydrocarbyl, halogen or a group -A-R3; R1 is hydrogen, C1-4 hydrocarbyl or a group -A-R3; provided that only one of R0 and R1 is a group -A-R3; R2 is hydrogen, C1-4 hydrocarbyl or halogen; A is a carbon- or heteroatom-containing linker group having a linking chain length of one or two atoms; R3 is a monocyclic or bicyclic heteroaryl group containing from five to twelve ring members; each group R4 is independently selected from hydrogen, hydroxy, halogen, nitro, cyano, a monocyclic heterocyclic group having up to seven ring members, a group N(R5)2, a group C(O)N(R6)2, a group S02N(R6)2, a group Ra-Rb and a group Y; provided that no more than one group Y is present; Ra is a bond, O, S, SO, S02, NH or N-C1-4 hydrocarbyl; Rb is C1-8 hydrocarbyl optionally interrupted by O, S, SO, SO2, NH or N-C1- 4 hydrocarbyl and optionally substituted by one or more substitutents selected from hydroxy, amino, mono- or di-C1-4 hydrocarbylamino, C1 -4 hydrocarbyloxy, oxo, C1 -4 hydrocarbylthio and halogen; each group R5 is independently selected from hydrogen, C1-4 alkyl, C1-4 acyl and C 1-4 alkylsulphonyl; each group R6 is independently selected from hydrogen and C1-4 hydrocarbyl; Y is a group -N(R7)-C(O)-R8 or -N(R7)_SO2-R8; R7 is hydrogen, C1-4 hydrocarbyl or a group C(O)-R8 or S02-R8; R8 is selected from C1-l0 hydrocarbyl, CI-10hydrocarbylamino, CI-10 hydrocarbylthio, C1-l0 hydrocarbyloxy, and aryl, arylamino, arylthio and aryloxy groups, the aryl moieties of which are carbocyclic or heterocyclic and have from five to twelve ring members, each substituent group R8 being optionally substituted by one or more groups R4 other than Y; or R7 and R8 together with the nitrogen and carbon or sulphur atoms to which they are attached are linked to form a ring structure of 4 to 7 ring members; wherein R0 is other than a 2-(2,4-diamino-6-triazinyl)ethyl group when, in combination, U, T, V and W are all CH, and R1 and R2 are both hydrogen; and provided that when the group -A-R3 contains an acidic substitituent group selected from carboxylic, phosphonic and sulphonic acids and tetrazoles, or contains a -C(O)NSO2- group, or when -A- is -C(O)N- and the nitrogen atom of the group A is linked directly to a furan or thiophene ring, then either R1 is -A-R3 and both R0 and R2 are hydrogen, or R0 is-A-R3 and R1 is hydrogen.

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