Welcome to LookChem.com Sign In|Join Free

CAS

  • or
1H-phosphole, 1,2,3,4,5-pentaphenyl-, 1-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1641-63-0 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1641-63-0 Structure
  • Basic information

    1. Product Name: 1H-phosphole, 1,2,3,4,5-pentaphenyl-, 1-oxide
    2. Synonyms: 1,2,3,4,5-Pentaphenyl-1H-phosphole 1-oxide
    3. CAS NO:1641-63-0
    4. Molecular Formula: C34H25OP
    5. Molecular Weight: 480.5355
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1641-63-0.mol
    9. Article Data: 4
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 710.654°C at 760 mmHg
    3. Flash Point: 383.59°C
    4. Appearance: N/A
    5. Density: 1.246g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.692
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1H-phosphole, 1,2,3,4,5-pentaphenyl-, 1-oxide(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1H-phosphole, 1,2,3,4,5-pentaphenyl-, 1-oxide(1641-63-0)
    12. EPA Substance Registry System: 1H-phosphole, 1,2,3,4,5-pentaphenyl-, 1-oxide(1641-63-0)
  • 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: 1641-63-0(Hazardous Substances Data)

1641-63-0 Usage

Phosphole oxide

A five-membered ring containing one phosphorus and one oxygen atom

Aromaticity

Highly aromatic molecule

Reactivity

Reactive molecule

Applications

Potential applications in organic synthesis and as a ligand in coordination chemistry

Substitution

Pentaphenyl substitution on the phosphole ring

Structural features

Interesting due to the pentaphenyl substitution

Electronic properties

Potential electronic properties

Heterocycle

A ring structure containing at least one heteroatom

Optoelectronic devices

Studied for potential use in organic light-emitting diodes and other optoelectronic devices

Check Digit Verification of cas no

The CAS Registry Mumber 1641-63-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,4 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1641-63:
(6*1)+(5*6)+(4*4)+(3*1)+(2*6)+(1*3)=70
70 % 10 = 0
So 1641-63-0 is a valid CAS Registry Number.

1641-63-0SDS

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 1,2,3,4,5-pentakis-phenyl-1λ<sup>5</sup>-phosphole 1-oxide

1.2 Other means of identification

Product number -
Other names 1H-Phosphole,1,2,3,4,5-pentaphenyl-,1-oxide

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:1641-63-0 SDS

1641-63-0Relevant articles and documents

High-Performance Synthesis of Phosphorus-Doped Graphene Materials and Stabilization of Phosphoric Micro- and Nanodroplets

Galushko, Alexey S.,Gordeev, Evgeniy G.,Ananikov, Valentine P.

, p. 15739 - 15748 (2019/01/04)

A thermally induced cascade process leading to the formation of stable micro- and nanometer-size phosphoric droplets was developed starting from a molecular precursor. Microwave-induced pyrolysis of 1,2,3,4,5-pentaphenylphosphole oxide proceeded through a

Structural and theoretical insights into the AIE attributes of phosphindole oxide: The balance between rigidity and flexibility

Bu, Fan,Wang, Erjing,Peng, Qian,Hu, Rongrong,Qin, Anjun,Zhao, Zujin,Tang, Ben Zhong

, p. 4440 - 4449 (2015/03/14)

Multiple intramolecular motions consume the excited-state energy of luminogenic molecules upon photoexcitation and lower the emission efficiency. The low frequency rotational motion of aromatic rings can be facilely restricted by steric constraint in the

Intense fluorescence of 1-aryl-2,3,4,5-tetraphenylphosphole oxides in the crystalline state

Fukazawa, Aiko,Ichihashi, Yasunori,Yamaguchi, Shigehiro

supporting information; experimental part, p. 1537 - 1540 (2010/10/03)

A series of 2,3,4,5-tetraphenylphosphole oxides with various aryl groups on the phosphorus atoms were synthesized and their fluorescence properties in the crystalline state were investigated. Some of these compounds showed an intense fluorescence with the

Cobalt Metallacycles. 8. Preparative and Kinetic Studies on the Reactivity of Cobaltacyclopentadienes with Phosphites

Yasufuku, Katsutoshi,Hamada, Akihiko,Aoki, Katsuyuki,Yamazaki, Hiroshi

, p. 4363 - 4372 (2007/10/02)

(η5-Cyclopentadienyl)(triphenylphosphine)cobaltacyclopentadiene complexes, (CoCR1=CR2CR3=CR4)(η5-C5H5)(PPh3) (1), react with phosphites, P(OR5)3 (2), yielding in successive steps (η5-cyclopentadienyl)(phosphite)cobaltacyclopentadiene complexes, (CoCR1=CR2CR3=CR4)(η5-C5H5)5)3> (3) and isomeric 1-alkoxyphosphole oxide complexes (4).The structure of one isomer of the 1-methoxyphosphole oxide complex, 4ca-2, was determined by an X-ray crystallographic structural analysis.The complexes 4, when oxidized by Ce4+ ions, give 1-alkoxyphosphole oxides.Kinetic studies on the formation of 3 and the conversion of 3 to 4 have been carried out and a first-order reaction has been verified in the complex concentration for both steps.Activation parameters for the reaction of 1c (R1, R2, R3, R4 = Ph) with 2a (OR5 = OCH3) are determined as ΔH(excit.) = 31 kcal mol-1 and ΔS(excit.) = 4 eu for the substitution, and as ΔH(excit.) = 22 kcal mol-1 and ΔS(excit.) = -4 eu for the conversion step, respectively.The preparative and kinetic investigations show that (1) both steric and electronic factors of the substituents of the cobalt metallacycles govern the substitution step, and (2) the electronic factor chiefly governs the conversion step.The steric effect of the alkyl groups of 2 is very distinctive in the conversion step.

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 1641-63-0