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[Ag{μ2-N,S-(1,3,5-triaza-7-phosphaadamantane)=NP(=S)(OPh)2}]x[SbF6]x is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1434146-62-9 Structure
  • Basic information

    1. Product Name: [Ag{μ2-N,S-(1,3,5-triaza-7-phosphaadamantane)=NP(=S)(OPh)2}]x[SbF6]x
    2. Synonyms:
    3. CAS NO:1434146-62-9
    4. Molecular Formula:
    5. Molecular Weight: 764.02
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1434146-62-9.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: [Ag{μ2-N,S-(1,3,5-triaza-7-phosphaadamantane)=NP(=S)(OPh)2}]x[SbF6]x(CAS DataBase Reference)
    10. NIST Chemistry Reference: [Ag{μ2-N,S-(1,3,5-triaza-7-phosphaadamantane)=NP(=S)(OPh)2}]x[SbF6]x(1434146-62-9)
    11. EPA Substance Registry System: [Ag{μ2-N,S-(1,3,5-triaza-7-phosphaadamantane)=NP(=S)(OPh)2}]x[SbF6]x(1434146-62-9)
  • 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: 1434146-62-9(Hazardous Substances Data)

1434146-62-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1434146-62-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,4,1,4 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1434146-62:
(9*1)+(8*4)+(7*3)+(6*4)+(5*1)+(4*4)+(3*6)+(2*6)+(1*2)=139
139 % 10 = 9
So 1434146-62-9 is a valid CAS Registry Number.

1434146-62-9Downstream Products

1434146-62-9Relevant articles and documents

New Ag(I)-iminophosphorane coordination polymers as efficient catalysts precursors for the MW-assisted meyer-schuster rearrangement of propargylic alcohols in water

Garcia-Alvarez, Joaquin,Diez, Josefina,Vidal, Cristian,Vicent, Cristian

, p. 6533 - 6542 (2013)

Treatment of the N-thiophosphorylated iminophosphorane ligands (PTA)=NP(=S)(OR)2 [PTA = 1,3,5-triaza-7-phosphaadamantane, 3a and 3b] and (DAPTA)=NP(=S)(OR)2 [DAPTA = 3,7-diacetyl-1,3,7-triaza-5- bicyclo[3.3.1]nonane, 4a and 4b] with an equimolecular amount of AgSbF 6 leads to high-yield formation of the new one-dimensional coordination polymers [Ag{μ2-N,S-(PTA)=NP(=S)(OR) 2}]x[SbF6]x (5a and 5b) and [Ag{μ2-O,S-(DAPTA)=NP(=S)(OR)2}]x[SbF 6]x (6a and 6b), respectively. These new (iminophosphorane)silver(I) coordination polymers are efficient catalyst precursors for the Meyer-Schuster isomerization of both terminal and internal alkynols. Reactions proceeded in water, under aerobic conditions and using microwave irradiation as heating source, to afford the corresponding α,β-unsaturated carbonyl compounds in excellent yields, without the addition of any cocatalyst. Remarkably, it should be noted that this catalytic system can be recycled up to 10 consecutive runs (1st cycle 45 min, 99%; 10th cycle 6 h, 97%). ESI-MS analysis of 5a in water has been carried out providing valuable insight into the monomeric active species responsible for catalytic activity in water.

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