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3-(1-Methyl-2-pyrrolidinyl)-1H-indole is a chemical compound with the molecular formula C13H16N2. It is a derivative of indole, a heterocyclic aromatic organic compound, and features a pyrrolidine ring attached to the indole structure. 3-(1-Methyl-2-pyrrolidinyl)-1H-indole is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various indole-based drugs and bioactive molecules. Its unique structure allows for the exploration of its properties and potential interactions with biological targets, making it a subject of interest in medicinal chemistry research.

7236-83-1

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7236-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7236-83-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,3 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7236-83:
(6*7)+(5*2)+(4*3)+(3*6)+(2*8)+(1*3)=101
101 % 10 = 1
So 7236-83-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H16N2/c1-15-8-4-7-13(15)11-9-14-12-6-3-2-5-10(11)12/h2-3,5-6,9,13-14H,4,7-8H2,1H3

7236-83-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1-methylpyrrolidin-2-yl)-1H-indole

1.2 Other means of identification

Product number -
Other names INDOLE,3-(1-METHYL-2-PYRROLIDINYL)

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:7236-83-1 SDS

7236-83-1Downstream Products

7236-83-1Relevant academic research and scientific papers

Selective Inhibition of Histone Deacetylase 10: Hydrogen Bonding to the Gatekeeper Residue is Implicated

Géraldy, Magalie,Morgen, Michael,Sehr, Peter,Steimbach, Raphael R.,Moi, Davide,Ridinger, Johannes,Oehme, Ina,Witt, Olaf,Malz, Mona,Nogueira, Mauro S.,Koch, Oliver,Gunkel, Nikolas,Miller, Aubry K.

, p. 4426 - 4443 (2019/05/17)

The discovery of isozyme-selective histone deacetylase (HDAC) inhibitors is critical for understanding the biological functions of individual HDACs and for validating HDACs as drug targets. The isozyme HDAC10 contributes to chemotherapy resistance and has

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