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1-(4-Phenylphenyl)isoquinoline, also known as PPIQ, is a heterocyclic chemical compound with a molecular formula of C25H17N. It features an isoquinoline core with a phenyl group attached at the 1-position and a 4-phenylphenyl group at the 4-position. PPIQ is recognized for its potential in medicinal chemistry, particularly in drug design and development, and has been investigated for its applications as an anti-cancer agent and a fluorescent probe for bioimaging. The unique structure and properties of PPIQ make it an intriguing and valuable compound for diverse research and development purposes.

110746-63-9

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110746-63-9 Usage

Uses

Used in Pharmaceutical Industry:
1-(4-Phenylphenyl)isoquinoline is used as a potential anti-cancer agent for its ability to target and disrupt cancer cell processes, thereby inhibiting tumor growth and progression.
Used in Bioimaging Applications:
1-(4-Phenylphenyl)isoquinoline is used as a fluorescent probe for its ability to bind with specific biological targets, enabling the visualization and monitoring of cellular processes and structures in real-time.
Used in Drug Design and Development:
1-(4-Phenylphenyl)isoquinoline is used as a key compound in the design and development of new drugs, leveraging its unique structure and properties to create novel therapeutic agents with improved efficacy and selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 110746-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,7,4 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 110746-63:
(8*1)+(7*1)+(6*0)+(5*7)+(4*4)+(3*6)+(2*6)+(1*3)=99
99 % 10 = 9
So 110746-63-9 is a valid CAS Registry Number.

110746-63-9SDS

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 1-(4-phenylphenyl)isoquinoline

1.2 Other means of identification

Product number -
Other names BIDD:GT0274

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:110746-63-9 SDS

110746-63-9Downstream Products

110746-63-9Relevant academic research and scientific papers

Visible Light Induced Rhodium(I)-Catalyzed C?H Borylation

Thongpaen, Jompol,Manguin, Romane,Dorcet, Vincent,Vives, Thomas,Duhayon, Carine,Mauduit, Marc,Baslé, Olivier

supporting information, p. 15244 - 15248 (2019/10/22)

An efficient visible light induced rhodium(I)-catalyzed regioselective borylation of aromatic C?H bonds is reported. The photocatalytic system is based on a single NHC?RhI complex capable of both harvesting visible light and enabling the bond breaking/forming at room temperature. The chelating nature of the NHC-carboxylate ligand was critical to ensure the stability of the RhI complex and to provide excellent photocatalytic activities. Experimental mechanistic studies evidenced a photooxidative ortho C?H bond addition upon irradiation with blue LEDs, leading to a cyclometalated RhIII-hydride intermediate.

Directed: Ortho C-H borylation catalyzed using Cp?Rh(iii)-NHC complexes

Thongpaen, Jompol,Schmid, Thibault E.,Toupet, Loic,Dorcet, Vincent,Mauduit, Marc,Baslé, Olivier

supporting information, p. 8202 - 8205 (2018/07/29)

Cp?Rh(NHC) complexes with bulky chiral bidentate NHC-carboxylate ligands were efficiently synthesized and fully characterized including solid-state structures. These unprecedented rhodium(iii) complexes demonstrated high selectivity in pyridine-directed ortho-C-H borylation of arenes under mild conditions.

Red emitter complexes of IR(III) and devices made with such compounds

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Page/Page column 13, (2008/06/13)

There are provided compounds of Formulae I and II: where: n is 1, 2 or 3;p is 0, 1 or 2;the sum of n +p is 3;R1 R2, R3 and R4 are each independently H, F, alkyl, trialkylsilyl, triarylsilyl, aryl or substituted

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