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108861-20-7

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  • SAGECHEM/ 1,1'-[1,4-PHENYLENEBIS(METHYLENE)]BIS(4,4'-BIPYRIDINIUM) BIS(HEXAFLUOROPHOSPHATE) /Manufacturer in China

    Cas No: 108861-20-7

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  • 4-pyridin-4-yl-1-[[4-[(4-pyridin-4-ylpyridin-1-ium-1-yl)methyl]phenyl]methyl]pyridin-1-ium,dihexafluorophosphate

    Cas No: 108861-20-7

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108861-20-7 Usage

Description

1,1'-(P-XYLYLENE)BIS(4,4'-BIPYRIDINIUM) BIS(HEXAFLUOROPHOSPHATE), also known as 1,1''-[1,4-Phenylenebis(methylene)]bis(4,4''-bipyridinium) bis(Hexafluorophosphate), is a chemical compound that serves as a valuable reactant in various chemical synthesis processes. Its unique structure and properties make it suitable for a range of applications across different industries.

Uses

Used in Chemical Synthesis:
1,1'-(P-XYLYLENE)BIS(4,4'-BIPYRIDINIUM) BIS(HEXAFLUOROPHOSPHATE) is used as a reactant in chemical synthesis for its ability to facilitate the formation of new compounds and contribute to the development of innovative materials and products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,1'-(P-XYLYLENE)BIS(4,4'-BIPYRIDINIUM) BIS(HEXAFLUOROPHOSPHATE) is used as a reactant for the synthesis of various drug molecules. Its unique properties allow for the creation of new compounds with potential therapeutic applications, contributing to the advancement of medicine and healthcare.
Used in Material Science:
1,1'-(P-XYLYLENE)BIS(4,4'-BIPYRIDINIUM) BIS(HEXAFLUOROPHOSPHATE) is also used in material science as a reactant for the development of new materials with specific properties. Its role in chemical synthesis enables the creation of materials with improved characteristics, such as enhanced stability, reactivity, or selectivity, which can be applied in various fields, including electronics, energy, and environmental protection.
Used in Research and Development:
In research and development, 1,1'-(P-XYLYLENE)BIS(4,4'-BIPYRIDINIUM) BIS(HEXAFLUOROPHOSPHATE) is utilized as a reactant to explore new chemical reactions and pathways. Its involvement in chemical synthesis aids scientists in understanding the underlying mechanisms and developing new methodologies, which can lead to breakthroughs in various scientific disciplines.

Check Digit Verification of cas no

The CAS Registry Mumber 108861-20-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,8,6 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 108861-20:
(8*1)+(7*0)+(6*8)+(5*8)+(4*6)+(3*1)+(2*2)+(1*0)=127
127 % 10 = 7
So 108861-20-7 is a valid CAS Registry Number.

108861-20-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-pyridin-4-yl-1-[[4-[(4-pyridin-4-ylpyridin-1-ium-1-yl)methyl]phenyl]methyl]pyridin-1-ium,dihexafluorophosphate

1.2 Other means of identification

Product number -
Other names P1407

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:108861-20-7 SDS

108861-20-7Downstream Products

108861-20-7Relevant articles and documents

Blurring the Lines between Host and Guest: A Chimeric Receptor Derived from Cucurbituril and Triptycene

Lu, Xiaoyong,Samanta, Soumen K.,Zavalij, Peter Y.,Isaacs, Lyle

, p. 8073 - 8078 (2018)

We report the synthesis and X-ray crystal structure of a cucurbituril–triptycene chimeric receptor (1). Host 1 binds to guests typical of CB[6]–CB[8], but also binds to larger guests such as blue box (20) and the Fujita square (22). Intriguingly, the geom

1,8-Dioxyanthracene-Derived Crown Ethers: Synthesis, Complexation with Paraquat and Assembly of a Tetracationic Cyclophane-Crown Ether Based [2]Catenane

Tang, Bo,Yang, Hong-Mei,Hu, Wen-Jing,Ma, Ming-Liang,Liu, Yahu A.,Li, Jiu-Sheng,Jiang, Biao,Wen, Ke

, p. 6925 - 6934 (2014)

1,8-Dioxyanthracene-based bisarylene crown ethers, composed of ethylene glycol chains and aromatic moieties, have been synthesized. Complexation studies revealed that these crown ethers could form 1:1 complexes with methyl viologen dication (N,N′-dimethyl

Cyclotris(paraquat-p-phenylenes)

Anamimoghadam, Ommid,Cooper, James A.,Nguyen, Minh T.,Guo, Qing-Hui,Mosca, Lorenzo,Roy, Indranil,Sun, Junling,Stern, Charlotte L.,Redfern, Louis,Farha, Omar K.,Stoddart, J. Fraser

, p. 13778 - 13783 (2019)

Reported here is the synthesis, solid-state characterization, and redox properties of new triangular, threefold symmetric, viologen-containing macrocycles. Cyclotris(paraquat-p-phenylene) (CTPQT6+) and cyclotris(paraquat-p-1,4-dimethoxyphenylen

ANALYTE DETECTION USING NEAR-INFRARED FLUOROPHORES

-

, (2016/08/29)

Embodiments of compounds for selectively detecting an analyte are disclosed, along with methods and kits for detecting analytes with the compounds. The compounds are bridged viologen conjugates including at least one fluorophore according to the general structure At least one of R1/R2, R2/R3, R3/R4, R5/R6, R6/R7, and/or R7/R8 together form a substituted or unsubstituted cycloalkyl or aryl.

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