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(E)-S-1-methyl-2-oxo-2-phenylethyl thiocinnamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 941568-95-2 Structure
  • Basic information

    1. Product Name: (E)-S-1-methyl-2-oxo-2-phenylethyl thiocinnamate
    2. Synonyms: (E)-S-1-methyl-2-oxo-2-phenylethyl thiocinnamate
    3. CAS NO:941568-95-2
    4. Molecular Formula:
    5. Molecular Weight: 296.39
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 941568-95-2.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: (E)-S-1-methyl-2-oxo-2-phenylethyl thiocinnamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-S-1-methyl-2-oxo-2-phenylethyl thiocinnamate(941568-95-2)
    11. EPA Substance Registry System: (E)-S-1-methyl-2-oxo-2-phenylethyl thiocinnamate(941568-95-2)
  • 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: 941568-95-2(Hazardous Substances Data)

941568-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 941568-95-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,1,5,6 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 941568-95:
(8*9)+(7*4)+(6*1)+(5*5)+(4*6)+(3*8)+(2*9)+(1*5)=202
202 % 10 = 2
So 941568-95-2 is a valid CAS Registry Number.

941568-95-2Downstream Products

941568-95-2Relevant articles and documents

Synthesis of multisubstituted furans, pyrroles, and thiophenes via ynolates

Shindo, Mitsuru,Yoshimura, Yutaka,Hayashi, Maiko,Soejima, Hiroe,Yoshikawa, Takashi,Matsumoto, Kenji,Shishido, Kozo

, p. 1963 - 1966 (2007)

An efficient synthetic method for the preparation of multisubstituted furans, thiophenes, and pyrroles using ynolates was developed. This novel formal [4 + 1] annulation by C2-C3 and C3-C4 bond formations Includes cycloaddition, cyclization, decarboxylati

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