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phenyl-3 propanedithioate de methyle is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104681-54-1 Structure
  • Basic information

    1. Product Name: phenyl-3 propanedithioate de methyle
    2. Synonyms: phenyl-3 propanedithioate de methyle
    3. CAS NO:104681-54-1
    4. Molecular Formula:
    5. Molecular Weight: 196.337
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104681-54-1.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: phenyl-3 propanedithioate de methyle(CAS DataBase Reference)
    10. NIST Chemistry Reference: phenyl-3 propanedithioate de methyle(104681-54-1)
    11. EPA Substance Registry System: phenyl-3 propanedithioate de methyle(104681-54-1)
  • 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: 104681-54-1(Hazardous Substances Data)

104681-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104681-54-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,6,8 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 104681-54:
(8*1)+(7*0)+(6*4)+(5*6)+(4*8)+(3*1)+(2*5)+(1*4)=111
111 % 10 = 1
So 104681-54-1 is a valid CAS Registry Number.

104681-54-1Relevant articles and documents

ANTIFUNGAL AGENTS

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Page/Page column 37, (2010/02/14)

Compounds of formula (I), and pharmaceutically acceptable salts thereof, may be used in therapy, for example as antifungal agents, wherein: R1, R2 and R3 are as defined herein. Certain compounds of formula (I) are also provided. Compounds of formula (I), and agriculturally acceptable salts thereof, may also be used as agricultural fungicides.

A new route to 1,1-difluoroolefins from carboxylic acids

Kim, Kyung-Il,McCarthy, James R.

, p. 3223 - 3226 (2007/10/03)

Methodology is described for the conversions of carboxylic acids to 1,1-difluoroolefins via α,α-difluorothioethers (3).

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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