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197314-10-6

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  • 197314-10-6 Structure

  • Basic information

    1. Product Name: 2-(3-benzoyl-phenyl)-thiopropionic acid S-methyl ester
    2. Synonyms: 2-(3-benzoyl-phenyl)-thiopropionic acid S-methyl ester
    3. CAS NO:197314-10-6
    4. Molecular Formula:
    5. Molecular Weight: 284.379
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 197314-10-6.mol
    9. Article Data: 1

  • 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-(3-benzoyl-phenyl)-thiopropionic acid S-methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(3-benzoyl-phenyl)-thiopropionic acid S-methyl ester(197314-10-6)
    11. EPA Substance Registry System: 2-(3-benzoyl-phenyl)-thiopropionic acid S-methyl ester(197314-10-6)

  • 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: 197314-10-6(Hazardous Substances Data)

197314-10-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 197314-10-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,3,1 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 197314-10:
(8*1)+(7*9)+(6*7)+(5*3)+(4*1)+(3*4)+(2*1)+(1*0)=146
146 % 10 = 6
So 197314-10-6 is a valid CAS Registry Number.

197314-10-6Downstream Products

197314-10-6Relevant articles and documents

An interesting synthetic application of S-alkyl (aryl)bis(alkylsulfanyl)thioacetates: General procedure for the preparation of (±)-α-arylpropionic acids

Clericuzio, Marco,Degani, Iacopo,Dughera, Stefano,Fochi, Rita

, p. 921 - 927 (2007/10/03)

Reported here is a new procedure for the synthesis of α-arylpropionic acids 1 in the racemic form, starting from derivatives of aromatic carboxylic acids 2 (i.e., esters), via 1-aryl-2,2,2-tris(alkylsulfanyl)ethanones 4-6, S-alkyl (aryl)bis(alkylsulfanyl)thioacetates 7-9, S-alkyl α-aryl-α-(alkylsulfanyl)thiopropionates 10-12 and S-alkyl α-arylthiopropionates 13-15. Each stage takes place easily and yields are always high.

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