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3-(2-diphenylphosphanylethylthio)phenylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1580443-44-2 Structure
  • Basic information

    1. Product Name: 3-(2-diphenylphosphanylethylthio)phenylamine
    2. Synonyms:
    3. CAS NO:1580443-44-2
    4. Molecular Formula:
    5. Molecular Weight: 337.425
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1580443-44-2.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-(2-diphenylphosphanylethylthio)phenylamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(2-diphenylphosphanylethylthio)phenylamine(1580443-44-2)
    11. EPA Substance Registry System: 3-(2-diphenylphosphanylethylthio)phenylamine(1580443-44-2)
  • 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: 1580443-44-2(Hazardous Substances Data)

1580443-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1580443-44-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,0,4,4 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1580443-44:
(9*1)+(8*5)+(7*8)+(6*0)+(5*4)+(4*4)+(3*3)+(2*4)+(1*4)=162
162 % 10 = 2
So 1580443-44-2 is a valid CAS Registry Number.

1580443-44-2Relevant articles and documents

Small molecule regulation of self-association and catalytic activity in a supramolecular coordination complex

McGuirk, C. Michael,Stern, Charlotte L.,Mirkin, Chad A.

, p. 4689 - 4696 (2014)

Herein, we report the synthesis and characterization of the first weak-link approach (WLA) supramolecular construct that employs the small molecule regulation of intermolecular hydrogen bonding interactions for the in situ control of catalytic activity. A biaryl urea group, prone to self-aggregation, was functionalized with a phosphinoalkyl thioether (P,S) hemilabile moiety and incorporated into a homoligated Pt(II) tweezer WLA complex. This urea-containing construct, which has been characterized by a single crystal X-ray diffraction study, can be switched in situ from a rigid fully closed state to a flexible semiopen state via Cl- induced changes in the coordination mode at the Pt(II) structural node. FT-IR and 1H NMR spectroscopy studies were used to demonstrate that while extensive urea self-association persists in the flexible semiopen complex, these interactions are deterred in the rigid, fully closed complex because of geometric and steric restraints. Consequently, the urea moieties in the fully closed complex are able to catalyze a Diels-Alder reaction between cyclopentadiene and methyl vinyl ketone to generate 2-acetyl-5-norbornene. The free urea ligand and the semiopen complex show no such activity. The successful incorporation and regulation of a hydrogen bond donating catalyst in a WLA construct open the doors to a vast and rapidly growing catalogue of allosteric catalysts for applications in the detection and amplification of organic analytes.

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