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21917-86-2

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21917-86-2 Usage

General Description

7,8-dihydroisoquinolin-5(6H)-one is a chemical compound that belongs to the isoquinoline family. It is a white to off-white solid that is soluble in organic solvents such as chloroform and ethanol. 7,8-DIHYDROISOQUINOLIN-5(6H)-ONE has been studied for its potential pharmacological properties, including its use as a precursor in the synthesis of various pharmaceuticals and natural products. 7,8-dihydroisoquinolin-5(6H)-one has also been investigated for its role as an intermediate in the synthesis of various bioactive compounds and may have potential applications in medicinal chemistry and drug discovery. Its chemical structure contains a fused ring system, making it an interesting candidate for further study in the fields of organic chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 21917-86-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,1 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21917-86:
(7*2)+(6*1)+(5*9)+(4*1)+(3*7)+(2*8)+(1*6)=112
112 % 10 = 2
So 21917-86-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO/c11-9-3-1-2-7-6-10-5-4-8(7)9/h4-6H,1-3H2

21917-86-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 7,8-dihydro-6H-isoquinolin-5-one

1.2 Other means of identification

Product number -
Other names 5-oxo-5,6,7,8-tetrahydroisoquinoline

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:21917-86-2 SDS

21917-86-2Relevant articles and documents

Molecular solar thermal systems-control of light harvesting and energy storage by protonation/deprotonation

Kilde, Martin Dr?hse,Arroyo, Paloma Garcia,Gertsen, Anders S.,Mikkelsen, Kurt V.,Nielsen, Mogens Br?ndsted

, p. 6356 - 6364 (2018)

Molecular solar thermal (MOST) systems that undergo photoisomerizations to long-lived, high-energy forms present one approach of addressing the challenge of solar energy storage. For this approach to mature, photochromic molecules which can absorb at the right wavelengths and which can store a sufficient amount of energy in a controlled time period have to be developed. Here we show in a combined experimental and theoretical study that incorporation of a pyridyl substituent onto the dihydroazulene/vinylheptafulvene photo-/thermoswitch results in molecules whose optical properties, energy-releasing back-reactions and energy densities can be controlled by protonation/deprotonation. The work thus presents a proof-of-concept for using acid/base to control the properties of MOST systems.

Combined Iron/Hydroxytriazole Dual Catalytic System for Site Selective Oxidation Adjacent to Azaheterocycles

Cooper, Julian C.,Luo, Chaosheng,Kameyama, Ryohei,Van Humbeck, Jeffrey F.

supporting information, p. 1243 - 1246 (2018/02/09)

This report details a new method for site-selective methylene oxidation adjacent to azaheterocycles. A dual catalysis approach, utilizing both an iron Lewis acid and an organic hydroxylamine catalyst, proved highly effective. We demonstrate that this method provides complementary selectivity to other known catalytic approaches and represents an improvement over current heterocycle-selective reactions that rely on stoichiometric activation.

PYRAZOLOISOQUINOLINE DERIVATIVES

-

Page/Page column 33, (2010/11/27)

New compounds of formula I, wherein the meanings for the various substituents are as disclosed in the description. These compounds are useful as p38 kinase inhibitors. (I)

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