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Triphenyl(2-quinolinylmethyl)-phosphoniumbromide is a versatile chemical compound used in organic synthesis, featuring a phosphonium cation with three phenyl groups and a 2-quinolinylmethyl group. It is typically found as a white crystalline solid, soluble in polar solvents like water and ethanol, and is renowned for its capacity to facilitate a range of organic reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds.

73870-26-5

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73870-26-5 Usage

Uses

Used in Organic Synthesis:
Triphenyl(2-quinolinylmethyl)-phosphoniumbromide is used as a catalyst or reagent for promoting various organic reactions, such as the formation of carbon-carbon and carbon-heteroatom bonds, due to its ability to enhance reaction rates and selectivity.
Used in Academic Research:
In academic research laboratories, Triphenyl(2-quinolinylmethyl)-phosphoniumbromide is utilized as a valuable tool for exploring new reaction pathways and mechanisms, contributing to the advancement of organic chemistry.
Used in Industrial Research:
Similarly, in industrial research settings, Triphenyl(2-quinolinylmethyl)-phosphoniumbromide is employed for its potential to improve the efficiency and effectiveness of chemical processes, leading to the development of new products and technologies in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 73870-26-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,7 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73870-26:
(7*7)+(6*3)+(5*8)+(4*7)+(3*0)+(2*2)+(1*6)=145
145 % 10 = 5
So 73870-26-5 is a valid CAS Registry Number.

73870-26-5SDS

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 triphenyl(quinolin-2-ylmethyl)phosphanium,bromide

1.2 Other means of identification

Product number -
Other names TRIPHENYL(2-QUINOLINYLMETHYL)-PHOSPHONIUMBROMIDE

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:73870-26-5 SDS

73870-26-5Relevant academic research and scientific papers

Phosphonium Ylide-Mediated Programmable Fluorination to Access Mono- And Difluoromethylarenes

Zheng, Yu,Xie, Zhen-Zhen,He, Xian-Chen,Chen, Yan-Shan,Cheng, Wen-Shuo,Chen, Kai,Xiang, Hao-Yue,Chen, Xiao-Qing,Yang, Hua

supporting information, p. 2538 - 2542 (2021/04/13)

Compounds bearing fluorinated moieties are pervasive in a wide range of pharmaceuticals and agrochemicals. The installation of fluorinated units is a persistently vital task in synthetic chemistry, where facile and manipulable assays are highly demanding.

CYCLOPENTYLBENZAMIDE DERIVATIVES AND THEIR USE FOR THE TREATMENT OF PSYCHOTIC AND COGNITIVE DISORDERS

-

, (2015/05/05)

The present invention provides compounds of formula (I) and pharmaceutically acceptable salts thereof, wherein n, L, X, Ra, Rb, R1, R2 and R3 their preparation, pharmaceutical compositions containing them and their use in therapy.

SUBSITUTED CYCLOPENTANES, TETRAHYDROFURANES AND PYRROLIDINES AS OREXIN RECEPTOR ANTAGONISTS

-

, (2015/09/28)

The present invention provides compounds of formula (I) and pharmaceutically acceptable salts thereof, Formula (I) wherein L,X, Ra, Rb, R 1, R2 and R3 are as defined in the specification, processes fo

Efficient synthesis of cis-2,6-di-(2-quinolylpiperidine)

Ding, Derong,Dwoskin, Linda P.,Crooks, Peter A.

, p. 5211 - 5213 (2013/09/02)

An efficient synthesis of cis-2,6-di-(2-quinolylpiperidine) has been developed. The key steps involve Wittig reaction of N-Cbz-protected cis-piperidine-2,6-dicarboxaldehyde (3) with 2-(triphenylphosphinyl-methyl) quinoline bromide (4) and sequential removal of the N-Cbz group and double bond reduction. This synthetic procedure provides an efficient preparation for this useful norlobelane analogue.

HETEROARYL COMPOUNDS AND METHODS OF USE THEREOF

-

Page/Page column 135, (2011/12/14)

Provided herein are heteroaryl compounds, methods of their synthesis, pharmaceutical compositions comprising the compounds, and methods of their use. In one embodiment, the compounds provided herein are useful for the treatment, prevention, and/or management of various disorders, such as CNS disorders and metabolic disorders, including, but not limited to, e.g., neurological disorders, psychosis, schizophrenia, obesity, and diabetes

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