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(E)-5-(4-methylthiostyryl)dihydrofuran-2(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1429328-73-3 Structure
  • Basic information

    1. Product Name: (E)-5-(4-methylthiostyryl)dihydrofuran-2(3H)-one
    2. Synonyms:
    3. CAS NO:1429328-73-3
    4. Molecular Formula:
    5. Molecular Weight: 234.319
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1429328-73-3.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)-5-(4-methylthiostyryl)dihydrofuran-2(3H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-5-(4-methylthiostyryl)dihydrofuran-2(3H)-one(1429328-73-3)
    11. EPA Substance Registry System: (E)-5-(4-methylthiostyryl)dihydrofuran-2(3H)-one(1429328-73-3)
  • 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: 1429328-73-3(Hazardous Substances Data)

1429328-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1429328-73-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,9,3,2 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1429328-73:
(9*1)+(8*4)+(7*2)+(6*9)+(5*3)+(4*2)+(3*8)+(2*7)+(1*3)=173
173 % 10 = 3
So 1429328-73-3 is a valid CAS Registry Number.

1429328-73-3Downstream Products

1429328-73-3Relevant articles and documents

Design, synthesis, in vitro cytotoxicity evaluation and structure-activity relationship of Goniothalamin analogs

Mohideen, Mazlin,Zulkepli, Suraya,Nik-Salleh, Nik-Salmah,Zulkefeli, Mohd,Weber, Jean-Frédéric Faizal Abdullah,Rahman, A. F. M. Motiur

, p. 812 - 831 (2013/07/26)

A series of six/five member (E/Z)-Goniothalamin analogs were synthesized from commercially available (3,4-dihydro-2H-pyran-2-yl)methanol/5- (hydroxymethyl)dihydrofuran-2(3H)-one in three steps with good to moderate overall yields and their cytotoxicity against lymphoblastic leukemic T cell line (Jurkat E6.1) have been evaluated. Among the synthesized analogs, (Z)-Goniothalamin appeared to be the most active in cytotoxicity (IC 50 = 12 μM). Structure-activity relationship study indicates that introducing substituent in phenyl ring or replacing phenyl ring by pyridine/naphthalene, or decreasing the ring size of lactones (from six to five member) do not increase the cytotoxicity.

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