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91025-04-6

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91025-04-6 Usage

General Description

2-Phenyl-3-(pyridin-2-yl)-1H-indole, also known as PPI, is a chemical compound with the molecular formula C20H14N2. It is a heterocyclic compound that contains an indole ring substituted with a phenyl group and a pyridine group at the 2 and 3 positions, respectively. PPI is a versatile molecule that has shown potential in various biological and chemical applications, including as a pharmaceutical intermediate, a building block for drug discovery, and a fluorescent probe in biochemical studies. Its unique structure and properties make it a valuable tool for researchers and chemists in the development of new drugs and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 91025-04-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,2 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91025-04:
(7*9)+(6*1)+(5*0)+(4*2)+(3*5)+(2*0)+(1*4)=96
96 % 10 = 6
So 91025-04-6 is a valid CAS Registry Number.

91025-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-3-pyridin-2-yl-1H-indole

1.2 Other means of identification

Product number -
Other names 2-Phenyl-3-[2]pyridyl-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:91025-04-6 SDS

91025-04-6Relevant articles and documents

2,3-Disubstituted indoles through the palladium-catalyzed reaction of aryl chlorides with o-alkynyltrifluoroacetanilides

Cacchi, Sandro,Fabrizi, Giancarlo,Goggiamani, Antonella

, p. 1301 - 1305 (2007/10/03)

2,3-Disubstituted indoles can be prepared in moderate to excellent yields by reacting readily available o-alkynyltrifluoroacetanilides with aryl chlorides in MeCN at 120°C in the presence of Pd2(dba)3 and Xphos.

2-Substituted 3-aryl- and 3-heteroarylindoles by the palladium-catalyzed reaction of o-trifluoroacetanilides with aryl bromides and triflates

Cacchi, Sandro,Fabrizi, Giancarlo,Lamba, Doriano,Marinelli, Fabio,Parisi, Luca M.

, p. 728 - 734 (2007/10/03)

The palladium-catalyzed reaction of aryl and heteroaryl bromides and triflates with o-alkynyltrifluoroacetanilides affords 2-substituted 3-aryl- and heteroarylindoles usually in excellent yield. The procedure can be applied to the synthesis of 2-substituted indole-3-carboxaldehydes.

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