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9H-Pyrido[3,4-b]indole, 1-ethyl-3-methyl-(9CI) is a chemical compound belonging to the pyridoindole family, characterized by a fused pyridine and indole ring system. This specific compound features an ethyl group at the 1-position and a methyl group at the 3-position, which are both substituents on the indole ring. It is an alkaloid, a type of naturally occurring organic compound that contains basic nitrogen atoms, and is often found in plants. The compound is represented by the chemical formula C12H12N2, indicating that it consists of 12 carbon atoms, 12 hydrogen atoms, and 2 nitrogen atoms. This particular compound is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or as a research tool due to its unique structure and properties.

401462-17-7

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401462-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 401462-17-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,1,4,6 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 401462-17:
(8*4)+(7*0)+(6*1)+(5*4)+(4*6)+(3*2)+(2*1)+(1*7)=97
97 % 10 = 7
So 401462-17-7 is a valid CAS Registry Number.

401462-17-7SDS

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 1-ethyl-3-methyl-9H-pyrido[3,4-b]indole

1.2 Other means of identification

Product number -
Other names -

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

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More Details:401462-17-7 SDS

401462-17-7Downstream Products

401462-17-7Relevant academic research and scientific papers

A short divergent approach to highly substituted carbazoles and β-carbolines via in situ-generated diketoindoles

Untergehrer, Martin,Bracher, Franz

, (2020)

Based on an aza-alkylation/Michael addition cascade reaction developed by Kim and co-workers we have developed divergent cascade reactions leading to either highly substituted 1-hydroxycarbazoles, 3-hydroxycarbazoles or β-carbolines, starting from readily

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