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1H-Indole-2-carboxaldehyde, 5-methyl-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41019-01-6

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41019-01-6 Usage

Derivative of indole

A heterocyclic aromatic organic compound

Used in synthesis

Various pharmaceuticals and agrochemicals, including potential anti-cancer agents

Potential applications

Organic chemistry building block for the production of more complex chemical compounds

Versatility

Highly versatile compound with potential applications in various industries

Check Digit Verification of cas no

The CAS Registry Mumber 41019-01-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,1 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 41019-01:
(7*4)+(6*1)+(5*0)+(4*1)+(3*9)+(2*0)+(1*1)=66
66 % 10 = 6
So 41019-01-6 is a valid CAS Registry Number.

41019-01-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-3-phenyl-indole-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5-Methyl-3-phenyl-1H-indole-2-carbaldehyde

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:41019-01-6 SDS

41019-01-6Relevant academic research and scientific papers

Synthesis of Substituted 7H-INdoloisoquinolines

Hiremath, Shiva Yogi P.,Badami, Prema S.,Purohit, Muralidhar G.

, p. 1235 - 1238 (2007/10/02)

Various substituted ethyl 3-phenylindole-2-carbamates (4a-f) have been synthesised through the intermediacy of carboxyhydrazides (2a-f) and carboxyazides (3a-f) and converted into 5,6-dihydro-7H-indoloisoquinolin-5(6H)-ones (5a-f) by refluxing in d

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