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94210-62-5

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94210-62-5 Usage

Physical state

Yellow to orange powder

Usage

Organic synthesis, reagent in chemical reactions

Applications

Preparation of indole derivatives, pharmaceuticals and agrochemicals development

Structure

Aromatic, contains functional groups

Versatility

Building block for complex organic molecules synthesis

Biological activities

Potential implications for drug discovery and development

Check Digit Verification of cas no

The CAS Registry Mumber 94210-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,2,1 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 94210-62:
(7*9)+(6*4)+(5*2)+(4*1)+(3*0)+(2*6)+(1*2)=115
115 % 10 = 5
So 94210-62-5 is a valid CAS Registry Number.
InChI:InChI=1/C19H13NO/c21-12-17-16-7-3-4-8-18(16)20-19(17)15-10-9-13-5-1-2-6-14(13)11-15/h1-12,20H

94210-62-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-naphthalen-2-yl-1H-indole-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2-naphthalen-2-yl-indole-3-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:94210-62-5 SDS

94210-62-5Downstream Products

94210-62-5Relevant articles and documents

Synthesis of 11H-indolo[3,2-c]quinolines by SnCl4-catalyzed cyclization of indole-3-carbaldehyde oximes

Aksenov,Gasanova,Prokonov, F. Yu.,Aksenov,Abakarov,Aksenov

, p. 2262 - 2270 (2020/02/15)

A new method for synthesizing 11H-indolo[3,2-c]quinolines by SnCl4-catalyzed intramolecular electrophilic amination of 2-arylindole-3-carbaldehyde O-acetyl oximes was developed.

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