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131370-05-3

Bis(dimethylaminophenylthiophosphoryl)sulfan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 131370-05-3 Structure

  • Basic information

    1. Product Name: Bis(dimethylaminophenylthiophosphoryl)sulfan
    2. Synonyms:
    3. CAS NO:131370-05-3
    4. Molecular Formula:
    5. Molecular Weight: 400.51
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 131370-05-3.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: Bis(dimethylaminophenylthiophosphoryl)sulfan(CAS DataBase Reference)
    10. NIST Chemistry Reference: Bis(dimethylaminophenylthiophosphoryl)sulfan(131370-05-3)
    11. EPA Substance Registry System: Bis(dimethylaminophenylthiophosphoryl)sulfan(131370-05-3)

  • 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: 131370-05-3(Hazardous Substances Data)

131370-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131370-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,3,7 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 131370-05:
(8*1)+(7*3)+(6*1)+(5*3)+(4*7)+(3*0)+(2*0)+(1*5)=83
83 % 10 = 3
So 131370-05-3 is a valid CAS Registry Number.

131370-05-3Downstream Products

131370-05-3Relevant articles and documents

UEBER DIE INSERTION VON RPS2 IN DIE PN-BINDUNG VON AMINOPHOSPHINEN

Diemert, K.,Hein, G.,Janssen, A.,Kuchen, W.

, p. 339 - 356 (2007/10/02)

Aminophosphines RnP(NR'2)3-n (n = 2, 1, 0; R = Ph, c-Hex, (-)Men, t-Bu; R' = Me, Et, n-Bu) react with 2,4-Bis(aryl)-1,3,2,4-dithiadiphosphetane-2,4-disulfides (ArPS2) (Ar: Ph, 4-Methoxyphenyl = An, Naphthyl, Thienyl) under formal insertion of monomeric (ArPS2)-units in one or in two of the λ3-P-N-bonds to yield chiral organophosphorus compounds Ar(R'2N)P(S)-S-PRn(NR'2)2-n (n = 2, 1, 0) and 2PRn(NR'2)1-n (n = 1, 0).At room temperature chiefly the λ3-P-N and λ3-P-S bonds in these products are solvolyzed by H2O or methanol with formation of mixtures of compounds.With hydrogen chloride An(Et2N)P(S)-S-PPh(NEt2) is converted into An(Et2N)P(S)-S-PPh(Cl).Addition of sulfur yields Ar(R'2N)P(S)-S-P(S)Rn(NR'2)2-n (n = 2, 1).Stereoisomerism of the new compounds is discussed and their structures as well as the composition of reaction mixtures are deduced from 31P-NMR-spectra.

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