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4-vinylbenzyl 1,3-oxathiolane-2-thione-5-ylmethyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1414436-28-4 Structure
  • Basic information

    1. Product Name: 4-vinylbenzyl 1,3-oxathiolane-2-thione-5-ylmethyl ether
    2. Synonyms: 4-vinylbenzyl 1,3-oxathiolane-2-thione-5-ylmethyl ether
    3. CAS NO:1414436-28-4
    4. Molecular Formula:
    5. Molecular Weight: 266.385
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1414436-28-4.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: 4-vinylbenzyl 1,3-oxathiolane-2-thione-5-ylmethyl ether(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-vinylbenzyl 1,3-oxathiolane-2-thione-5-ylmethyl ether(1414436-28-4)
    11. EPA Substance Registry System: 4-vinylbenzyl 1,3-oxathiolane-2-thione-5-ylmethyl ether(1414436-28-4)
  • 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: 1414436-28-4(Hazardous Substances Data)

1414436-28-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1414436-28-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,4,4,3 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1414436-28:
(9*1)+(8*4)+(7*1)+(6*4)+(5*4)+(4*3)+(3*6)+(2*2)+(1*8)=134
134 % 10 = 4
So 1414436-28-4 is a valid CAS Registry Number.

1414436-28-4Downstream Products

1414436-28-4Relevant articles and documents

Synthesis and radical polymerization of styrene-based monomer having a five-membered cyclic dithiocarbonate structure

Miyata, Takahiro,Matsumoto, Kozo,Endo, Takeshi,Yonemori, Shigeaki,Watanabe, Shoji

, p. 1398 - 1404 (2013)

A styrene-based monomer having a five-membered cyclic dithiocarbonate structure, 4-vinylbenzyl 1,3-oxathiolane-2-thione-5-ylmethyl ether (VBTE), was synthesized from 4-vinylbenzyl glycidyl ether (VBGE) and carbon disulfide in the presence of lithium bromide in 86% yield. Radical polymerization of VBTE in dimethyl sulfoxide by 2,2′-azobisisobutyronitrile was carried out at 60 °C to afford the corresponding the polymer, polyVBTE, in 64% yield. PolyVBTE with number-averaged molecular weight higher than 31,000 was obtained. The glass transition temperature (Tg) and 5 wt % decomposition temperature (Td5) of the polyVBTE were evaluated to be 66 and 264 °C under nitrogen atmosphere by differential scanning calorimetry and thermal gravimetry analysis, respectively. It was confirmed that a polymer consisting of the same VBTE repeating unit could also be obtained via polymer reaction, that is, a lithium bromide-catalyzed addition of carbon disulfide to a polyVBGE prepared from a radical polymerization of VBGE. Copolymerization of VBTE and styrene with various compositions efficiently gave copolymers of VBTE and styrene.

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