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104090-73-5

2-biphenylylacetothiomorpholide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104090-73-5 Structure

  • Basic information

    1. Product Name: 2-biphenylylacetothiomorpholide
    2. Synonyms: 2-biphenylylacetothiomorpholide
    3. CAS NO:104090-73-5
    4. Molecular Formula:
    5. Molecular Weight: 297.421
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104090-73-5.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: 2-biphenylylacetothiomorpholide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-biphenylylacetothiomorpholide(104090-73-5)
    11. EPA Substance Registry System: 2-biphenylylacetothiomorpholide(104090-73-5)

  • 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: 104090-73-5(Hazardous Substances Data)

104090-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104090-73-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,0,9 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104090-73:
(8*1)+(7*0)+(6*4)+(5*0)+(4*9)+(3*0)+(2*7)+(1*3)=85
85 % 10 = 5
So 104090-73-5 is a valid CAS Registry Number.

104090-73-5Downstream Products

104090-73-5Relevant articles and documents

Substituted 1,3,4-Thiadiazoles with Anticonvulsant Activity. 2. Aminoalkyl Derivatives

Stillings, Michael R.,Welbourn, Anthony P.,Walter, Donald S.

, p. 2280 - 2284 (2007/10/02)

This paper describes the synthesis and pharmacological evaluation of a number of substituted 1,3,4-thiadiazoles.The first member of the series, 2-(aminomethyl)-5-(2-biphenylyl)-1,3,4-thiadiazole (7) was found to possess potent anticonvulsant properties in rats and mice and compared favorably with the standard anticonvulsant drugs phenytoin, phenobarbital, and carbamazepine in a number of test situations.The potency of compound 7 was maintained on alkylation of the side-chain nitrogen atom; however, aryl substitution or chain lengthening caused a drop in potency.Replacement of the 2-biphenylyl group by phenyl or benzyl also lead to inactive compounds.

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