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78428-92-9

3-ethyl-4-(phenylthio)butyric acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 78428-92-9 Structure

  • Basic information

    1. Product Name: 3-ethyl-4-(phenylthio)butyric acid
    2. Synonyms:
    3. CAS NO:78428-92-9
    4. Molecular Formula:
    5. Molecular Weight: 224.324
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 78428-92-9.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: 3-ethyl-4-(phenylthio)butyric acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-ethyl-4-(phenylthio)butyric acid(78428-92-9)
    11. EPA Substance Registry System: 3-ethyl-4-(phenylthio)butyric acid(78428-92-9)

  • 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: 78428-92-9(Hazardous Substances Data)

78428-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78428-92-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,2 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78428-92:
(7*7)+(6*8)+(5*4)+(4*2)+(3*8)+(2*9)+(1*2)=169
169 % 10 = 9
So 78428-92-9 is a valid CAS Registry Number.

78428-92-9Relevant articles and documents

New Synthetic Route for the Preparation of 4-Phenylthio-4-butanolide Derivatives by the Use of the Pummerer Rearrangement

Watanabe, Mikio,Nakamori, Seijin,Hasegawa, Hatsue,Shirai, Kozo,Kumamoto, Takanobu

, p. 817 - 821 (2007/10/02)

The Pummerer rearrangement reaction of 2- or 3-substituted 4-(phenylsulfinyl)butyric acids in the presence of an excess amount of acetic anhydride and a catalytic amount of p-toluenesulfonic acid in refluxing toluene for 1 h afforded 2- or 3-substituted 4-phenylthio-4-butanolide (17a-f).Thermolysis in pyridine of 4-phenylsulfinyl 4-butanolides, which were prepared by oxidation of 17a-f, afforded 2- or 3-substituted 2- or 3-buten-4-olides.

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