60669-22-9

Basic information

• Product Name: (1-UNDECYL)TRIPHENYLPHOSPHONIUM BROMIDE, 98+%
• Synonyms: (1-UNDECYL)TRIPHENYLPHOSPHONIUM BROMIDE, 98+%;n-Undecyl triphenylphosphonium bromide;N-UNDECYL TRIPHENYLPHOSPONIUM BROMIDE;Undecyltriphenylphosphonium·bromide
• CAS NO: 60669-22-9
• Molecular Formula: Br*C₂₉H₃₈P
• Molecular Weight: 497.489781
• EINECS: 262-363-3
• Mol File: 60669-22-9.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (1-UNDECYL)TRIPHENYLPHOSPHONIUM BROMIDE, 98+%(CAS DataBase Reference)
• NIST Chemistry Reference: (1-UNDECYL)TRIPHENYLPHOSPHONIUM BROMIDE, 98+%(60669-22-9)
• EPA Substance Registry System: (1-UNDECYL)TRIPHENYLPHOSPHONIUM BROMIDE, 98+%(60669-22-9)

Safety Data

• Statements: R36/37/38:Irritating to eyes, respiratory system and skin.
• Safety Statements: S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.; S36:Wear suitable prot
• Hazardous Substances Data: 60669-22-9(Hazardous Substances Data)

Usage

Description

(1-Undecyl)triphenylphosphonium bromide, 98+% is a high purity organic compound that features a phosphonium cation and a bromide anion. It is widely recognized for its applications in various fields, including organic synthesis, pharmaceutical research, material development, and organic electronics.
Used in Organic Synthesis:
(1-Undecyl)triphenylphosphonium bromide, 98+% is used as a phase-transfer catalyst for facilitating reactions in organic synthesis. Its ability to transfer reactants between different phases improves reaction efficiency and product yields.
Used in Pharmaceutical Research:
In pharmaceutical research, (1-Undecyl)triphenylphosphonium bromide, 98+% is utilized as an antimicrobial agent. Its effectiveness against various microorganisms makes it a valuable component in the development of new antimicrobial drugs and treatments.
Used in Material Development:
(1-Undecyl)triphenylphosphonium bromide, 98+% is used as a component in the development of new materials. Its unique properties contribute to the creation of innovative materials with potential applications in various industries.
Used in Organic Electronics:
In the field of organic electronics, (1-Undecyl)triphenylphosphonium bromide, 98+% is used for its potential applications in the development of electronic devices and components. Its properties make it a promising candidate for enhancing the performance of organic electronic systems.
Overall, the high purity of (1-Undecyl)triphenylphosphonium bromide, 98+% makes it an ideal choice for research and industrial applications where precise and consistent results are essential.

InChI:InChI=1/C29H38P.BrH/c1-2-3-4-5-6-7-8-9-19-26-30(27-20-13-10-14-21-27,28-22-15-11-16-23-28)29-24-17-12-18-25-29;/h10-18,20-25H,2-9,19,26H2,1H3;1H/q+1;/p-1

Upstream product

• 693-67-4 bromoundecane 
• 603-35-0 triphenylphosphine 

Downstream Products

• 87269-78-1 undecylidenetriphenylphosphorane 
• 161615-36-7 (4Z,2R,3R)-2,3-O-Isopropylidene-4-pentadecen-1-ol benzyl ether 
• 123-08-0 4-hydroxy-benzaldehyde 
• 92991-44-1 (Z)-methyl 3-<4-(1-dodecenyl)phenoxy>propanoate 
• 92991-43-0 (E)-methyl 3-<4-(1-dodecenyl)phenoxy>propanoate 
• 172339-02-5 (S)-2-Benzoylamino-2-[(4R,5R)-2,2-dimethyl-5-((Z)-tridec-2-enyl)-[1,3]dioxolan-4-yl]-3-methoxymethoxy-propionic acid methyl ester 
• 172339-01-4 (S)-2-Benzoylamino-2-[(4R,5R)-2,2-dimethyl-5-((E)-tridec-2-enyl)-[1,3]dioxolan-4-yl]-3-methoxymethoxy-propionic acid methyl ester 
• 181863-88-7 ethyl (1)-4-(1-dodecenyl)-α-phenyl-1H-pyrazole-1-acetate 
• 1530-29-6 1,1-diphenyl-dodec-1-ene 
• 1026489-01-9 tert-Butyl-[((E)-hexadec-5-enyl)oxy]-diphenyl-silane 

Relevant articles and documents

Parallel, stereoselective syntheses of both enantiomers of muricatacin and their sulfur and nitrogen relatives using the silyloxy diene-based methodology

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A yellow star longicorn pheromone preparation method (by machine translation)

The present invention provides a preparation method of huang xing longicorn pheromone, the present invention relates to chiral compound compound 1 as the initial reactant, and selecting different quaternary phosphonium salt, can be efficient and rapid growth of the aliphatic, obtained with high stereo specific hued rectangle which bears longicorn pheromone. The present invention provides a preparation method of the operation is simple, short synthetic route, and the goal overall yield of the product is high, up to 20% (as the compound 1 is calculated as the initiator), is suitable for the large scale synthesis, the beetles of the pheromone huang xing active research, biological experiment, agricultural applications and pest control of important significance. (by machine translation)

Development of sulfonamide AKT PH domain inhibitors

Disruption of the phosphatidylinositol 3-kinase/AKT signaling pathway can lead to apoptosis in cancer cells. Previously we identified a lead sulfonamide that selectively bound to the pleckstrin homology (PH) domain of AKT and induced apoptosis when present at low micromolar concentrations. To examine the effects of structural modification, a set of sulfonamides related to the lead compound was designed, synthesized, and tested for binding to the expressed PH domain of AKT using a surface plasmon resonance-based competitive binding assay. Cellular activity was determined by means of an assay for pAKT production and a cell killing assay using BxPC-3 cells. The most active compounds in the set are lipophilic and possess an aliphatic chain of the proper length. Results were interpreted with the aid of computational modeling. This paper represents the first structure-activity relationship (SAR) study of a large family of AKT PH domain inhibitors. Information obtained will be used in the design of the next generation of inhibitors of AKT PH domain function.