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1779-51-7

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1779-51-7 Usage

Chemical Properties

white crystalline powder

Uses

Different sources of media describe the Uses of 1779-51-7 differently. You can refer to the following data:
1. suzuki reaction
2. Reactant for: Free radical 5-exo-dig cyclization Intramolecular hydroacylalkoxylation Wittig reactions for stereoselective synthesis of alkenes Dimerization of α-olefins Alkylidenation of hydrazides for synthesis of indoles Tandem cyclization and 1,2-thiolate shift of nitrogen ylides
3. n-Butyltriphenylphosphonium Bromide is used in the synthesis of inhibitors of tubulin polymerization thus expressing antimitotic and antitubulin properties. Also used in the synthesis of 3-phenylpropanoic acids as peroxisome proliferator-activated receptor dual agonists affecting the mitochondrial carnitine system.

Check Digit Verification of cas no

The CAS Registry Mumber 1779-51-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,7 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1779-51:
(6*1)+(5*7)+(4*7)+(3*9)+(2*5)+(1*1)=107
107 % 10 = 7
So 1779-51-7 is a valid CAS Registry Number.
InChI:InChI=1/C22H25P.BrH/c1-2-3-19-23(20-13-7-4-8-14-20,21-15-9-5-10-16-21)22-17-11-6-12-18-22;/h4-18,23H,2-3,19H2,1H3;1H

1779-51-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (B0970)  Butyltriphenylphosphonium Bromide  >98.0%(HPLC)(T)

  • 1779-51-7

  • 25g

  • 290.00CNY

  • Detail
  • TCI America

  • (B0970)  Butyltriphenylphosphonium Bromide  >98.0%(HPLC)(T)

  • 1779-51-7

  • 250g

  • 1,690.00CNY

  • Detail
  • Alfa Aesar

  • (A10504)  (1-Butyl)triphenylphosphonium bromide, 99%   

  • 1779-51-7

  • 25g

  • 234.0CNY

  • Detail
  • Alfa Aesar

  • (A10504)  (1-Butyl)triphenylphosphonium bromide, 99%   

  • 1779-51-7

  • 100g

  • 736.0CNY

  • Detail
  • Alfa Aesar

  • (A10504)  (1-Butyl)triphenylphosphonium bromide, 99%   

  • 1779-51-7

  • 500g

  • 3378.0CNY

  • Detail
  • Aldrich

  • (B102806)  Butyltriphenylphosphoniumbromide  99%

  • 1779-51-7

  • B102806-100G

  • 983.97CNY

  • Detail

1779-51-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name butyl(triphenyl)phosphanium,bromide

1.2 Other means of identification

Product number -
Other names butyl(triphenyl)phosphoniumbromid

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:1779-51-7 SDS

1779-51-7Relevant articles and documents

Two Are Better Than One: A Design Principle for Ultralong-Persistent Luminescence of Pure Organics

Alam, Parvej,Leung, Nelson L. C.,Liu, Junkai,Cheung, Tsz Shing,Zhang, Xuepeng,He, Zikai,Kwok, Ryan T. K.,Lam, Jacky W. Y.,Sung, Herman H. Y.,Williams, Ian D.,Chan, Christopher C. S.,Wong, Kam Sing,Peng, Qian,Tang, Ben Zhong

, (2020)

Because of their innate ability to store and then release energy, long-persistent luminescence (LPL) materials have garnered strong research interest in a wide range of multidisciplinary fields, such as biomedical sciences, theranostics, and photonic devices. Although many inorganic LPL systems with afterglow durations of up to hours and days have been reported, organic systems have had difficulties reaching similar timescales. In this work, a design principle based on the successes of inorganic systems to produce an organic LPL (OLPL) system through the use of a strong organic electron trap is proposed. The resulting system generates detectable afterglow for up to 7 h, significantly longer than any other reported OLPL system. The design strategy demonstrates an easy methodology to develop organic long-persistent phosphors, opening the door to new OLPL materials.

-

Yamamoto,Oku

, p. 509,511 (1954)

-

Lipophilic ion aromaticity is not important for permeability across lipid membranes

Aleksandrova, Ekaterina V.,Antonenko, Yuri N.,Kirsanov, Roman S.,Korshunova, Galina A.,Kotova, Elena A.,Luzhkov, Victor B.,Rokitskaya, Tatyana I.,Tashlitsky, Vadim N.

, (2021)

To clarify the contribution of charge delocalization in a lipophilic ion to the efficacy of its permeation through a lipid membrane, we compared the behavior of alkyl derivatives of triphenylphosphonium, tricyclohexylphosphonium and trihexylphosphonium bo

Phosphonium-based ionic liquids: Economic and efficient catalysts for the solvent-free cycloaddition of CO2 to epoxidized soybean vegetable oil to obtain potential bio-based polymers precursors

Centeno-Pedrazo, A.,Freixa, Z.,Garcia-Suarez, E. J.,Perez-Arce, J.,Prieto-Fernandez, S.

, (2021/10/01)

A series of phosphonium-based ionic liquids have been prepared in one step in a simple way from inexpensive feedstocks. The prepared ionic liquids have been successfully tested as catalysts in the solvent-free cycloaddition reaction of CO2 to an epoxidized soybean oil to obtain carbonated soybean oil that can be potentially employed as bio-monomer in the synthesis for bio-based polymers. The catalytic performance of these ionic liquids was compared to the widely used and benchmark catalyst in CO2 cycloaddition to epoxides reaction, namely tetrabutylammonium bromide at different reaction conditions. The influence of some reaction parameters such as temperature, CO2 pressure, reaction time and catalyst amount was studied. It has been found that the solubility of the prepared ionic liquids in the reaction media (epoxidized soybean oil) is a key factor that limits the catalytic performance of some of the synthesized ionic liquids. All prepared ionic liquids have shown higher thermal stability that the benchmark catalyst and three of them have shown superior catalytic performance. The best results in terms of conversion and selectivity have been obtained with dodecyltriphenylphosphonium bromide (5) achieving almost full conversion (99.8%) and excellent selectivity (84.0%) after 5 h reaction at 160 oC and 40 bar of CO2. Outstanding results compared to those reported in the literature with similar catalysts in the solvent-free CO2 cycloaddtion to an epoxidized soybean oil to obtain the corresponding carbonated oil have been achieved. Considering the facile synthesis of catalyst 5, the large availability and non-expensive of the feedstocks and its catalytic performance it can be considered a valuable and green alternative for CO2 fixation to epoxidized vegetable oil.

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