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ethyl 2,2-diethoxy-3-{[(4-methylphenyl)sulfonyl]oxy}propanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1604814-03-0 Structure
  • Basic information

    1. Product Name: ethyl 2,2-diethoxy-3-{[(4-methylphenyl)sulfonyl]oxy}propanoate
    2. Synonyms: ethyl 2,2-diethoxy-3-{[(4-methylphenyl)sulfonyl]oxy}propanoate
    3. CAS NO:1604814-03-0
    4. Molecular Formula:
    5. Molecular Weight: 360.428
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1604814-03-0.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: ethyl 2,2-diethoxy-3-{[(4-methylphenyl)sulfonyl]oxy}propanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2,2-diethoxy-3-{[(4-methylphenyl)sulfonyl]oxy}propanoate(1604814-03-0)
    11. EPA Substance Registry System: ethyl 2,2-diethoxy-3-{[(4-methylphenyl)sulfonyl]oxy}propanoate(1604814-03-0)
  • 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: 1604814-03-0(Hazardous Substances Data)

1604814-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1604814-03-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,4,8,1 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1604814-03:
(9*1)+(8*6)+(7*0)+(6*4)+(5*8)+(4*1)+(3*4)+(2*0)+(1*3)=140
140 % 10 = 0
So 1604814-03-0 is a valid CAS Registry Number.

1604814-03-0Downstream Products

1604814-03-0Relevant articles and documents

[18F]Fluoropyruvate: Radiosynthesis and initial biological evaluation

Graham, Keith,Mueller, Andre,Lehmann, Lutz,Koglin, Norman,Dinkelborg, Ludger,Siebeneicher, Holger

, p. 164 - 171 (2014)

The radiosynthesis of [18F]fluoropyruvate was investigated using numerous precursors were synthesized from ethyl 2,2-diethoxy-3- hydroxypropanoate (5) containing different leaving groups: mesylate, tosylate, triflate, and nonaflate. These precursors were evaluated for [ 18F]fluoride incorporation with triflate being superior. The subsequent hydrolysis step was investigated, and an acidic hydrolysis was optimized. After establishing suitable purification and formulation methods, the [18F]fluoropyruvate could be isolated in ca. 50% d.c. yield. The [18F]fluoropyruvate was evaluated in vitro for its uptake into tumor cells using adenocarcinomic human alveolar basal epithelial cells (A549) and unfortunately showed an uptake of approximately 0.1% of the applied dose per 100,000 cells after 30 min. Initial pharmacokinetic properties were assessed in vivo using nude mice showed a high degree of bone uptake from defluorination, which will limit its potential as an imaging agent for metabolic processes. Copyright

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