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CAS

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61680-00-0

O,O-dipropyl phosphoroisothiocyanatidothioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 61680-00-0 Structure

  • Basic information

    1. Product Name: O,O-dipropyl phosphoroisothiocyanatidothioate
    2. Synonyms: O,O-dipropyl phosphoroisothiocyanatidothioate
    3. CAS NO:61680-00-0
    4. Molecular Formula:
    5. Molecular Weight: 239.299
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 61680-00-0.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: O,O-dipropyl phosphoroisothiocyanatidothioate(CAS DataBase Reference)
    10. NIST Chemistry Reference: O,O-dipropyl phosphoroisothiocyanatidothioate(61680-00-0)
    11. EPA Substance Registry System: O,O-dipropyl phosphoroisothiocyanatidothioate(61680-00-0)

  • 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: 61680-00-0(Hazardous Substances Data)

61680-00-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61680-00-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,8 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61680-00:
(7*6)+(6*1)+(5*6)+(4*8)+(3*0)+(2*0)+(1*0)=110
110 % 10 = 0
So 61680-00-0 is a valid CAS Registry Number.

61680-00-0Relevant articles and documents

REACTIONS OF DIALKYL DITHIOPHOSPHORIC AND DIPHENYLDITHIOPHOSPHORIC ACIDS WITH THIOCYANATES

Zimin, M. G.,Kamalov, R. M.,Cherkasov, R. A.,Pudovik, A. N.

, p. 371 - 378 (2007/10/02)

The interaction between phosphorus(IV) dithio acid partial esters and thiocyanates proceeds with initial formation of addition products to the CN bond.These adducts are either split by the second molecule of dithio acid to S-alkyl dithiocarbamates and tetraalkyl trithiophosphates or rearrange into dialkyl N-thiophosphoryldithiocarbamates.The latter easily split off the thiols and convert to isothiocyanatothiophosphates.A number of thiophosphorylated and diphosphorylated thioureas were synthesized by the reaction of isothiocyanatothiophosphates with amines and α-aminoalkylphosphonates.

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