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7333-63-3

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7333-63-3 Usage

Description

(4-Bromobutyl)triphenylphosphonium bromide is a chemical compound that serves as a versatile reagent in various organic synthesis and chemical reactions. It is characterized by its bromoalkyl chain and triphenylphosphonium cation, which contribute to its unique properties and applications.

Uses

Used in Organic Synthesis:
(4-Bromobutyl)triphenylphosphonium bromide is used as a reactant in various organic synthesis processes, including azidification, C-H activation and β-elimination to produce an eight-membered ring system, and 1,3-dipolar cycloaddition of azides onto alkenes. Its reactivity and stability make it a valuable component in the synthesis of complex organic molecules.
Used in Stereoselective SmI2-mediated Coupling:
In the field of stereoselective reactions, (4-Bromobutyl)triphenylphosphonium bromide is used as a reactant in SmI2-mediated coupling of unsaturated carbonyl compounds and aldehydes. This application allows for the formation of specific stereoisomers, which is crucial in the development of enantioselective synthetic routes.
Used in Synthesis of D-labeled Methylenecyclobutane:
(4-Bromobutyl)triphenylphosphonium bromide is also utilized in the synthesis of D-labeled methylenecyclobutane, a valuable intermediate in the production of various pharmaceuticals and agrochemicals. Its involvement in this synthesis process highlights its versatility and importance in the field of organic chemistry.
Used in Coupling Reactions:
As a reactant in coupling reactions, (4-Bromobutyl)triphenylphosphonium bromide plays a crucial role in the formation of new chemical bonds and the synthesis of a wide range of compounds. Its ability to participate in various coupling reactions further demonstrates its utility in organic synthesis.
Used in the Synthesis of Cell-Penetrating Peptoids with Cationic Side Chains:
(4-Bromobutyl)triphenylphosphonium bromide is used in the synthesis of cell-penetrating peptoids with cationic side chains, which have potential applications in the delivery of therapeutic agents and diagnostic tools. Its role in the development of these peptoids underscores its importance in the field of medicinal chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 7333-63-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,3 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7333-63:
(6*7)+(5*3)+(4*3)+(3*3)+(2*6)+(1*3)=93
93 % 10 = 3
So 7333-63-3 is a valid CAS Registry Number.
InChI:InChI=1/C22H23BrP/c23-18-10-11-19-24(20-12-4-1-5-13-20,21-14-6-2-7-15-21)22-16-8-3-9-17-22/h1-9,12-17H,10-11,18-19H2/q+1

7333-63-3 Well-known Company Product Price

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  • Alfa Aesar

  • (B23040)  (4-Bromobutyl)triphenylphosphonium bromide, 98%   

  • 7333-63-3

  • 10g

  • 307.0CNY

  • Detail
  • Alfa Aesar

  • (B23040)  (4-Bromobutyl)triphenylphosphonium bromide, 98%   

  • 7333-63-3

  • 50g

  • 1039.0CNY

  • Detail

7333-63-3SDS

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 (4-Bromobutyl)triphenylphosphonium bromide

1.2 Other means of identification

Product number -
Other names Phosphonium, (4-bromobutyl)triphenyl-, bromide

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:7333-63-3 SDS

7333-63-3Relevant articles and documents

A diketopyrrolopyrrole-based fluorescent probe for investigating mitochondrial zinc ions

Du, Chenchen,Fu, Shibo,Ren, Xiaolei,Wang, Xiaohua,Wang, Zhong,Zhou, Juan,Wang, Hongyu

, p. 3493 - 3502 (2018)

We demonstrate a strategy to asymmetrically introduce a Zn2+ chelator (MeO-DPEN) and a mitochondrial-targeting group (TPP) at the N-positions of both lactam moieties of diketopyrrolopyrrole (DPP) fluorophore. And two probes DPP-Mito and DPP-C2

A mitochondria-targeted thiazoleorange-based photothermal agent for enhanced photothermal therapy for tumors

Bian, Wangqing,Pan, Zhenxing,Wang, Yakun,Long, Wei,Chen, Zefeng,Chen, Niping,Zeng, Yaoxun,Yuan, Jiongpeng,Liu, Xujie,Lu, Yu-Jing,He, Yan,Zhang, Kun

, (2021)

Organic small molecules with near-infrared (NIR) absorption hold great promise as the phototheranostic agents for clinical translation by virtue of their inherent merits such as well-defined chemical structure, high purity and good reproducibility. Probes

Fluorescent Probe HKSOX-1 for imaging and detection of endogenous superoxide in live cells and in vivo

Hu, Jun Jacob,Wong, Nai-Kei,Ye, Sen,Chen, Xingmiao,Lu, Ming-Yang,Zhao, Angela Qian,Guo, Yuhan,Ma, Alvin Chun-Hang,Leung, Anskar Yu-Hung,Shen, Jiangang,Yang, Dan

, p. 6837 - 6843 (2015)

Superoxide anion radical (O2-) is undoubtedly the most important primary reactive oxygen species (ROS) found in cells, whose formation and fate are intertwined with diverse physiological and pathological processes. Here we report a highly sensitive and selective O2- detecting strategy involving O2- cleavage of an aryl trifluoromethanesulfonate group to yield a free phenol. We have synthesized three new O2- fluorescent probes (HKSOX-1, HKSOX-1r for cellular retention, and HKSOX-1m for mitochondria-targeting) which exhibit excellent selectivity and sensitivity toward O2- over a broad range of pH, strong oxidants, and abundant reductants found in cells. In confocal imaging, flow cytometry, and 96-well microplate assay, HKSOX-1r has been robustly applied to detect O2- in multiple cellular models, such as inflammation and mitochondrial stress. Additionally, our probes can be efficiently applied to visualize O2- in intact live zebrafish embryos. These probes open up exciting opportunities for unmasking the roles of O2- in health and disease.

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

, (2020/05/06)

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.

A SET OF MITOCHONDRIA-TARGETED COMPOUNDS

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Page/Page column 11, (2019/01/17)

Here are described SkQ compounds containing cations of various types: alkyl(triphenyl)phosphonium cation, quaternary ammonium cations, including pH -dependent and permanent cations of rhodamines, berberine and palmatine alkaloids.

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