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1(2H)-Isoquinolinone, 3,4-dihydro-3-phenyl-2-(phenylmethyl)is a chemical compound with the molecular formula C24H21NO. It is a derivative of isoquinolinone featuring a phenylmethyl substitution at the 2-position and a phenyl group at the 3-position. 1(2H)-Isoquinolinone, 3,4-dihydro-3-phenyl-2-(phenylmethyl)is known for its potential biological and pharmacological activities, making it a subject of interest in pharmaceutical research and drug development.

108762-64-7

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108762-64-7 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
1(2H)-Isoquinolinone, 3,4-dihydro-3-phenyl-2-(phenylmethyl)is utilized as a compound in pharmaceutical research and drug development due to its potential biological and pharmacological properties. Its unique structure and activity make it a promising candidate for the development of new therapeutic agents.
Used in Pain Relief and Neurological Disorders:
In the medical field, 1(2H)-Isoquinolinone, 3,4-dihydro-3-phenyl-2-(phenylmethyl)is used as a potential therapeutic agent for pain relief and neurological disorders. Its analgesic and neuroprotective properties are being investigated for their effectiveness in treating various conditions related to pain and neurological damage.
Used in Insecticidal and Pest Control Applications:
1(2H)-Isoquinolinone, 3,4-dihydro-3-phenyl-2-(phenylmethyl)also has potential applications in the agricultural industry as an insecticide or pest control agent. Its insecticidal and pest control properties are being studied for their effectiveness in managing and controlling pests that can damage crops and affect agricultural productivity.
Used in Chemical Synthesis:
In the chemical industry, 1(2H)-Isoquinolinone, 3,4-dihydro-3-phenyl-2-(phenylmethyl)may be used as a starting material or intermediate in the synthesis of various other compounds with different applications, such as pharmaceuticals, agrochemicals, or specialty chemicals. Its unique structure and reactivity make it a valuable component in the development of new chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 108762-64-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,7,6 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108762-64:
(8*1)+(7*0)+(6*8)+(5*7)+(4*6)+(3*2)+(2*6)+(1*4)=137
137 % 10 = 7
So 108762-64-7 is a valid CAS Registry Number.

108762-64-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-3-phenyl-3,4-dihydroisoquinolin-1-one

1.2 Other means of identification

Product number -
Other names 1(2H)-Isoquinolinone,3,4-dihydro-3-phenyl-2-(phenylmethyl)

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:108762-64-7 SDS

108762-64-7Downstream Products

108762-64-7Relevant academic research and scientific papers

Synthesis of 3-Substituted and 3,4-Disubstituted 3,4-Dihydro-1(2H)-isoquinolones by Condensation of Lithiated N,N-Diethyl-o-toluamide with Imines

Clark, Robin D.,Jahangir

, p. 5378 - 5382 (2007/10/02)

Lithiated N,N-diethyl-o-toluamide was condensed with imines to afford 3,4-dihydro-1(2H)-isoquinolones.The products were deprotonated under the reaction conditions, and electrophilic trapping afforded trans-2,3,4-trisubstituted-2,3-dihydro-1(2H)-isoquinolones.This methodology was also applied to the synthesis of 7-substituted 7,8-dihydro-1,6-naphthyridin-5(6H)-ones.

Enamide Photochemistry. A Convenient Synthesis of 3-Aryl-1-oxotetrahydro- and dihydro-Isoquinolines (Isocarbostyrils)

Couture, Axel,Grandclaudon, Pierre

, p. 576 - 578 (2007/10/02)

Irradiation of enamides 1 gave 3-aryl-1-oxotetrahydroisoquinolines 3 in good yields.Use of iodine led to the formation of dihydroisoquinolines 4.

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