Welcome to LookChem.com Sign In|Join Free

CAS

  • or
(6-PHTHALIMIDOHEXYL)TRIPHENYLPHOSPHONIUM BROMIDE, with the chemical formula C30H29BrNO2P, is a phosphonium salt that features a phthalimide group and a hexyl chain. (6-PHTHALIMIDOHEXYL)TRIPHENYLPHOSPHONIUM BROMIDE is recognized for its role as a phase transfer catalyst and as a reactant in organic synthesis, where it facilitates a range of reactions including nucleophilic substitution, alkylations, and Michael additions.

129789-59-9 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 129789-59-9 Structure
  • Basic information

    1. Product Name: (6-PHTHALIMIDOHEXYL)TRIPHENYLPHOSPHONIUM BROMIDE
    2. Synonyms: 6-(1,3-dioxoisoindolin-2-yl)hexyl-triphenyl-phosphonium bromide
    3. CAS NO:129789-59-9
    4. Molecular Formula: Br*C32H31NO2P
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 129789-59-9.mol
  • Chemical Properties

    1. Melting Point: 74-76°C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. Sensitive: Hygroscopic
    10. CAS DataBase Reference: (6-PHTHALIMIDOHEXYL)TRIPHENYLPHOSPHONIUM BROMIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: (6-PHTHALIMIDOHEXYL)TRIPHENYLPHOSPHONIUM BROMIDE(129789-59-9)
    12. EPA Substance Registry System: (6-PHTHALIMIDOHEXYL)TRIPHENYLPHOSPHONIUM BROMIDE(129789-59-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 129789-59-9(Hazardous Substances Data)

129789-59-9 Usage

Uses

Used in Organic Synthesis:
(6-PHTHALIMIDOHEXYL)TRIPHENYLPHOSPHONIUM BROMIDE is used as a reactant for its ability to participate in various organic reactions, such as nucleophilic substitutions, alkylations, and Michael additions. Its unique structure allows it to act as a catalyst, enhancing the efficiency and selectivity of these reactions.
Used in Pharmaceutical Preparation:
In the pharmaceutical industry, (6-PHTHALIMIDOHEXYL)TRIPHENYLPHOSPHONIUM BROMIDE is used as a reactant in the preparation of various organic compounds and pharmaceuticals. Its versatility in facilitating different types of chemical reactions makes it a valuable component in the synthesis of a wide array of medicinal compounds.
Used as a Phase Transfer Catalyst:
(6-PHTHALIMIDOHEXYL)TRIPHENYLPHOSPHONIUM BROMIDE is utilized as a phase transfer catalyst to expedite reactions between reactants in two immiscible phases, typically an aqueous and an organic phase. This property is particularly useful in industrial processes where efficient mixing and reaction rates are crucial for the production of desired compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 129789-59-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,7,8 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 129789-59:
(8*1)+(7*2)+(6*9)+(5*7)+(4*8)+(3*9)+(2*5)+(1*9)=189
189 % 10 = 9
So 129789-59-9 is a valid CAS Registry Number.
InChI:InChI=1/C32H31NO2P.BrH/c34-31-29-22-12-13-23-30(29)32(35)33(31)24-14-1-2-15-25-36(26-16-6-3-7-17-26,27-18-8-4-9-19-27)28-20-10-5-11-21-28;/h3-13,16-23H,1-2,14-15,24-25H2;1H/q+1;/p-1

129789-59-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (B25034)  (6-Phthalimidohexyl)triphenylphosphonium bromide, 94%   

  • 129789-59-9

  • 5g

  • 664.0CNY

  • Detail
  • Alfa Aesar

  • (B25034)  (6-Phthalimidohexyl)triphenylphosphonium bromide, 94%   

  • 129789-59-9

  • 25g

  • 2604.0CNY

  • Detail
  • Alfa Aesar

  • (B25034)  (6-Phthalimidohexyl)triphenylphosphonium bromide, 94%   

  • 129789-59-9

  • 100g

  • 7694.0CNY

  • Detail

129789-59-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (6-PHTHALIMIDOHEXYL)TRIPHENYLPHOSPHONIUM BROMIDE

1.2 Other means of identification

Product number -
Other names 6-(1,3-dioxoisoindol-2-yl)hexyl-triphenylphosphanium,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:129789-59-9 SDS

129789-59-9Relevant articles and documents

SYNERGISTIC INIHIBITION OF TUMOR CELL PROLIFERATION INDUCED BY COMBINED TREATMENT OF METFORMIN COMPOUNDS AND IRON CHELATORS

-

Paragraph 00106-00107, (2018/07/29)

The present invention is directed to combination therapy comprising metformin or mito-metformin compounds with at least one iron chelating agent for the treatment of cancer and pharmaceutical compositions thereof.

MODIFIED MITO-METFORMIN COMPOUNDS AND METHODS OF SYNTHESIS AND USE THEREOF

-

Paragraph 0088; 0089, (2016/02/29)

The present invention provides mito-metformin compounds, pharmaceutical compositions thereof, and methods of using the mito-metformin compounds in the treatment of cancer.

Phosphonium lipocations as antiparasitic agents

Long, Timothy E.,Lu, Xiao,Galizzi, Melina,Docampo, Roberto,Gut, Jiri,Rosenthal, Philip J.

scheme or table, p. 2976 - 2979 (2012/06/04)

Phosphonium lipocations were synthesized and evaluated for inhibition of the development of Plasmodium falciparum and Trypanosoma cruzi, etiological agents of malaria and Chagas disease, respectively. Optimal phthalimides and 1,4-naphthoquinone-based lipocations were active in vitro at mid-high nM concentrations against P. falciparum and low μM concentrations against T. cruzi.

ENZYME INHIBITORS AND THE USE THEREOF

-

Page/Page column 30; 31, (2010/04/03)

The present invention provides compounds and methods for the treatment of diseases or disorders such as heart failure, hyperlipidemia, hypercholesterolemia, gonadotropin deficiency, diabetes mellitus, metabolic syndrome, hyperglycemia, insulin resistance,

Synthesis of bridged dinucleosides

Agathocleous, Demetrios C.,Bulman Page, Philip C.,Cosstick, Richard,Galpin, Ian J.,McLennan, Alexander G.,Prescott, Mark

, p. 2047 - 2058 (2007/10/02)

A series of di-(adenosin-N6-yl) alkanes (1b) - (11) has been prepared by reaction of the appropriate diaminoalkanes with 6-chloro-9-β-D-(2,3,5-tri-O-acetyl)-ribofuranosyl-purine (2) followed by ammonolysis. Alternatively, an analogous reaction with 6-chloro-9-β-D-(2,3-O-isopropylidene)-ribofuranosylpurine (3) produced an intermediate which could be phosphorylated at the 5′-position prior to hydrolytic removal of the isopropylidene group. 4-(1,2,4-Triazolo)-1-(β-D-2,3,5-tri-O-acetyl ribofuranosyl)-2(1H)-pyrimidone (7) was an effective intermediate for the preparation of di-(cytidin-N4-yl) alkanes (8a), (8b), and (8c) from the appropriate diaminoalkanes. The longer chain di-(adenosin-N6-yl) alkanes are very effective inhibitors of adenosine kinase. In addition an approach to the di-(adenosin-N6-yl) alkanes is described which should allow tritium labelling of the alkyl chain.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 129789-59-9