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17952-63-5

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17952-63-5 Usage

Description

6-METHOXY-1 2 3 4-TETRAHYDRO-9H-PYRIDO-&, also known as 6-Methoxy-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-1-carboxylic Acid, is a chemical compound with a unique molecular structure. It is characterized by its tetrahydro-9H-pyrido[3,4-b]indole framework and a methoxy group at the 6th position. 6-METHOXY-1 2 3 4-TETRAHYDRO-9H-PYRIDO-& is known for its ability to act as a stain or dye, making it a valuable asset in various applications.

Uses

Used in Staining and Dyeing Applications:
6-METHOXY-1 2 3 4-TETRAHYDRO-9H-PYRIDO-& is used as a stain/dye for its ability to impart color to various materials. The compound's chemical structure allows it to bind with other molecules, making it an effective coloring agent in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 6-METHOXY-1 2 3 4-TETRAHYDRO-9H-PYRIDO-& is used as a metabolite for research and development purposes. Its unique chemical properties make it a valuable compound for studying various biological processes and developing new drugs.
Used in Research and Development:
6-METHOXY-1 2 3 4-TETRAHYDRO-9H-PYRIDO-& is also used in research and development for its potential applications in various fields. Its chemical properties and reactivity make it an interesting subject for further study and potential use in the development of new materials, compounds, or processes.

Check Digit Verification of cas no

The CAS Registry Mumber 17952-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,5 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17952-63:
(7*1)+(6*7)+(5*9)+(4*5)+(3*2)+(2*6)+(1*3)=135
135 % 10 = 5
So 17952-63-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H14N2O3/c1-18-7-2-3-10-9(6-7)8-4-5-14-12(13(16)17)11(8)15-10/h2-3,6,12,14-15H,4-5H2,1H3,(H,16,17)

17952-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methoxy-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6-methoxy-1,2,3,4-tetrahydronorharman-1-carboxylic acid

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:17952-63-5 SDS

17952-63-5Relevant articles and documents

Peganumine A alkaloid structure simplifier and application thereof

-

Paragraph 0037-0041; 0056-0058, (2021/06/26)

The invention discloses a Peganumine A alkaloid structure simplifier, a stereoisomer or a pharmaceutical salt thereof. The structure is shown in the following general formula: each substituent group is defined in the specification. The simplified structure of the Peganumine A alkaloid provided by the invention has a relatively obvious proliferation inhibition effect on liver cancer HepG2, lung cancer A549 and intestinal cancer HCT116, and the anti-tumor activity of part of compounds is higher than the anti-liver cancer HepG2 activity of Peganumine A reported in literatures.

6-Hydroxy- and 6-methoxy-β-carbolines as acetyl- and butyrylcholinesterase inhibitors

Schott, Yvonne,Decker, Michael,Rommelspacher, Hans,Lehmann, Jochen

, p. 5840 - 5843 (2007/10/03)

In the course of studies directed toward the discovery of novel acetyl- and butyrylcholinesterase (AChE and BChE) inhibitors for the treatment of Alzheimer's disease, we focused on β-carbolines (BCs). 6-Oxygenated β-carboline and β-carbolinium derivatives based on the serotonin template were synthesized and tested in vitro for their ability to inhibit AChE and BChE, respectively. Particularly the carbolinium salts, which can be formed by intracerebral methylation out of the tertiary-BC prodrugs, show inhibitory activity levels reaching those of galantamine, physostigmine, and rivastigmine.

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