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

53603-64-8

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53603-64-8 Usage

Type of compound

Nitroso compound

Structure

Nitroso group attached to the 3rd carbon and a phenyl group attached to the 2nd carbon of the indole ring

Usage

Building block in organic synthesis, potential applications in medicinal and pharmaceutical chemistry

Biological activities

Studied for potential activities, may be relevant in the development of new drugs or as a chemical intermediate in organic synthesis

Documentation

Specific properties, uses, and potential risks not widely documented in scientific literature.

Check Digit Verification of cas no

The CAS Registry Mumber 53603-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,0 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53603-64:
(7*5)+(6*3)+(5*6)+(4*0)+(3*3)+(2*6)+(1*4)=108
108 % 10 = 8
So 53603-64-8 is a valid CAS Registry Number.

53603-64-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethyl-3-nitroso-2-phenyl-indole

1.2 Other means of identification

Product number -
Other names 1-Aethyl-3-nitroso-2-phenyl-indol

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:53603-64-8 SDS

53603-64-8Relevant academic research and scientific papers

Rh(III)-Catalyzed Tandem Acylmethylation/Nitroso Migration/Cyclization of N-Nitrosoanilines with Sulfoxonium Ylides in One Pot: Approach to 3-Nitrosoindoles

Wu, Yingtao,Pi, Chao,Cui, Xiuling,Wu, Yangjie

supporting information, p. 361 - 364 (2020/02/04)

A novel synthesis of 3-nitrosoindoles starting from easily available N-nitrosoanilines and sulfoxonium ylides via Rh(III)-catalyzed acylmethylation and trifluoroacetic acid (TFA)-mediated nitroso transfer/cyclization cascade reaction in one pot has been d

Preparation method of 3-nitroso substituted indole derivative

-

Paragraph 0059-0062; 0158-0161, (2019/12/12)

The invention belongs to the technical field of organic synthesis and particularly relates to a preparation method of a 3-nitroso substituted indole derivative. The preparation method comprises the following steps: mixing N-nitrosoaniline as shown in a fo

N-nitrosodiphenylamine as an alternative nitrosating agent for indoles

Cardellini,Greci,Stipa

, p. 677 - 682 (2007/10/02)

N-nitrosodiphenylamine reacts in the presence of catalytic amounts of trichloroacetic acid with indoles forming the corresponding nitroso and isonitroso derivatives in good yields.

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