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15582-97-5

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15582-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15582-97-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,8 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15582-97:
(7*1)+(6*5)+(5*5)+(4*8)+(3*2)+(2*9)+(1*7)=125
125 % 10 = 5
So 15582-97-5 is a valid CAS Registry Number.

15582-97-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-4,5,6,7-tetrahydro-1H-indole

1.2 Other means of identification

Product number -
Other names 2-Phenyl-4.5.6.7-tetrahydro-1H-benzo<b>pyrrol

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:15582-97-5 SDS

15582-97-5Relevant articles and documents

A Small-Molecule Inhibitor of Prion Replication and Mutant Prion Protein Toxicity

Massignan, Tania,Sangiovanni, Valeria,Biggi, Silvia,Stincardini, Claudia,Elezgarai, Saioa R.,Maietta, Giulia,Andreev, Ivan A.,Ratmanova, Nina K.,Belov, Dmitry S.,Lukyanenko, Evgeny R.,Belov, Grigory M.,Barreca, Maria Letizia,Altieri, Andrea,Kurkin, Alexander V.,Biasini, Emiliano

supporting information, p. 1286 - 1292 (2017/09/01)

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Efficient Trapping of 1,2-Cyclohexadienes with 1,3-Dipoles

Lofstrand, Verner A.,West, Frederick G.

supporting information, p. 10763 - 10767 (2016/07/27)

1,2-Cyclohexadienes are transient intermediates that undergo rapid dimerization and intermolecular trapping with activated olefins and heteroatomic nucleophiles. Fluoride-mediated desilylative elimination of readily accessible 6-silylcyclohexene-1-triflates allows the mild, chemoselective, and functional-group tolerant generation of cyclic allene intermediates, which undergo efficient trapping reactions with stable 1,3-dipoles. The reactions proceed with high levels of both regio- and diastereoselectivity. The reaction of cyclic allenes with azides is accompanied by the facile loss of dinitrogen, resulting in the formation of tetrahydroindoles or polycylic aziridines depending on the azide employed.

General and regioselective synthesis of pyrroles via ruthenium-catalyzed multicomponent reactions

Zhang, Min,Fang, Xianjie,Neumann, Helfried,Beller, Matthias

supporting information, p. 11384 - 11388 (2013/08/23)

A general and highly regioselective synthesis of pyrroles via ruthenium-catalyzed three-component reactions has been developed. A variety of ketones including less reactive aryl and alkyl substrates were efficiently converted in combination with different

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