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1198151-82-4

methylthiophosphonic acid O-butyl-O-(3-diphenylthiophosphoryl)phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1198151-82-4 Structure

  • Basic information

    1. Product Name: methylthiophosphonic acid O-butyl-O-(3-diphenylthiophosphoryl)phenyl ester
    2. Synonyms: methylthiophosphonic acid O-butyl-O-(3-diphenylthiophosphoryl)phenyl ester
    3. CAS NO:1198151-82-4
    4. Molecular Formula:
    5. Molecular Weight: 460.538
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1198151-82-4.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: methylthiophosphonic acid O-butyl-O-(3-diphenylthiophosphoryl)phenyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: methylthiophosphonic acid O-butyl-O-(3-diphenylthiophosphoryl)phenyl ester(1198151-82-4)
    11. EPA Substance Registry System: methylthiophosphonic acid O-butyl-O-(3-diphenylthiophosphoryl)phenyl ester(1198151-82-4)

  • 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: 1198151-82-4(Hazardous Substances Data)

1198151-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1198151-82-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,1,5 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1198151-82:
(9*1)+(8*1)+(7*9)+(6*8)+(5*1)+(4*5)+(3*1)+(2*8)+(1*2)=174
174 % 10 = 4
So 1198151-82-4 is a valid CAS Registry Number.

1198151-82-4Relevant articles and documents

Thiophosphoryl-, thiophosphoryloxy-, and thiophosphorylamino-benzene derivatives as novel classes of hybrid pincer ligands

Kozlov, Vladimir A.,Aleksanyan, Diana V.,Vasilev, Andrei A.,Odinets, Irina L.

, p. 626 - 637 (2011/06/22)

The synthetic approaches to novel families of SCE (E = S',N,O) hybrid pincertype ligands bearing thophosphoryl, thiophosphoryloxy, and thiophosphorylamino groups in various combinations with thiophosphoryl-, thiocarbamoyl-, and imine- (including that of benzothiazole ring) donating functions have been developed. All of the ligands readily undergo direct cyclometallation (metal = Pd(II), Pt(II)) to afford 5,5- or 5,6-membered pincer complexes. Palladium complexes displayed from high to excellent catalytic performance in the Suzuki cross-coupling reaction of aryl bromides and phenylboronic acid and the higher asymmetry for a complex served as a factor of its higher catalytic activity. Copyright Taylor & Francis Group, LLC.

5,6-Membered palladium pincer complexes of 1-thiophosphoryloxy-3- thiophosphorylbenzenes. Synthesis, X-ray structure, and catalytic activity

Kozlov,Aleksanyan,Nelyubina, Yu. V.,Lyssenko,Gutsul,Vasil'Ev,Petrovskii,Odinets

, p. 8657 - 8666 (2011/01/08)

Novel unsymmetrical ligands, 1-thiophosphoryloxy-3-thiophosphorylbenzenes 3a-d, bearing phosphine sulfide and thiophosphoryloxy moieties as coordinating sites, were found to undergo cyclometalation at the C-2 position of the central benzene ring in a reac

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