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63985-67-1

(3-phenoxypropyl)(triphenyl)phosphonium is a chemical compound that consists of a phosphonium cation with three phenyl groups attached to it, along with a 3-phenoxypropyl group. It is known for its ability to facilitate the transfer of reactants between different phases, making it a versatile component in various chemical processes.

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  • 63985-67-1 Structure

  • Basic information

    1. Product Name: (3-phenoxypropyl)(triphenyl)phosphonium
    2. Synonyms:
    3. CAS NO:63985-67-1
    4. Molecular Formula: Br*C27H26OP
    5. Molecular Weight: 397.468
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 63985-67-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (3-phenoxypropyl)(triphenyl)phosphonium(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3-phenoxypropyl)(triphenyl)phosphonium(63985-67-1)
    11. EPA Substance Registry System: (3-phenoxypropyl)(triphenyl)phosphonium(63985-67-1)

  • 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: 63985-67-1(Hazardous Substances Data)

63985-67-1 Usage

Uses

Used in Organic Synthesis:
(3-phenoxypropyl)(triphenyl)phosphonium is used as a phase-transfer catalyst for facilitating the transfer of reactants from one phase to another in organic synthesis. This enhances the efficiency and effectiveness of a variety of reactions, including nucleophilic substitution, oxidation, and Wittig reactions.
Used in Pharmaceutical Research:
In the field of pharmaceutical research, (3-phenoxypropyl)(triphenyl)phosphonium is utilized in the design and synthesis of potential antimicrobial and antitumor agents. Its unique properties allow for the development of new compounds with therapeutic potential, contributing to advancements in medicine and healthcare.

Check Digit Verification of cas no

The CAS Registry Mumber 63985-67-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,9,8 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63985-67:
(7*6)+(6*3)+(5*9)+(4*8)+(3*5)+(2*6)+(1*7)=171
171 % 10 = 1
So 63985-67-1 is a valid CAS Registry Number.

63985-67-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenoxypropyl(triphenyl)phosphanium,bromide

1.2 Other means of identification

Product number -
Other names Phosphonium,(3-phenoxypropyl)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:63985-67-1 SDS

63985-67-1Relevant articles and documents

Improved cyclobutyl nabilone analogs as potent CB1 receptor agonists

Papanastasiou, Ioannis P.,Georgiadis, Markos-Orestis,Iliopoulos-Tsoutsouvas, Christos,Paronis, Carol A.,Brust, Christina A.,Tran, Ngan K.,Ji, Lipin,Ma, Xiaoyu,Wood, JodiAnne T.,Zvonok, Nikolai,Tong, Fei,Bohn, Laura M.,Nikas, Spyros P.,Makriyannis, Alexandros

supporting information, (2022/01/20)

In earlier work, we explored the SAR for the C3 side chain pharmacophore in the hexahydrocannabinol template represented by the drug nabilone, which resulted in the development of AM2389. In an effort for further optimization, we have merged features of n

2-CYCLOALKYL RESORCINOL CANNABINERGIC LIGANDS

-

Paragraph 0179, (2014/05/07)

The present invention relates to novel 2-cycloalkyl resorcinol compounds; to pharmaceutical compositions comprising the compounds; and to methods of preparing the compounds and uses thereof. The disclosed compounds can bind to and modulate the cannabinoid

Novel 1′,1′-chain substituted hexahydrocannabinols: 9β-hydroxy-3-(1-hexyl-cyclobut-1-yl)-hexahydrocannabinol (AM2389) a highly potent cannabinoid receptor 1 (CB1) agonist

Nikas, Spyros P.,Alapafuja, Shakiru O.,Papanastasiou, Ioannis,Paronis, Carol A.,Shukla, Vidyanand G.,Papahatjis, Demetris P.,Bowman, Anna L.,Halikhedkar, Aneetha,Han, Xiuwen,Makriyannis, Alexandros

experimental part, p. 6996 - 7010 (2010/12/18)

In pursuit of a more detailed understanding of the structural requirements for the key side chain cannabinoid pharmacophore, we have extended our SAR to cover a variety of conformationally modified side chains within the 9-keto and 9-hydroxyl tricyclic st

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