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90199-05-6

4-tetrahydrofuran-2-yl-but-3-en-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 90199-05-6 Structure

  • Basic information

    1. Product Name: 4-tetrahydrofuran-2-yl-but-3-en-2-one
    2. Synonyms: 4-tetrahydrofuran-2-yl-but-3-en-2-one
    3. CAS NO:90199-05-6
    4. Molecular Formula:
    5. Molecular Weight: 140.182
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 90199-05-6.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-tetrahydrofuran-2-yl-but-3-en-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-tetrahydrofuran-2-yl-but-3-en-2-one(90199-05-6)
    11. EPA Substance Registry System: 4-tetrahydrofuran-2-yl-but-3-en-2-one(90199-05-6)

  • 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: 90199-05-6(Hazardous Substances Data)

90199-05-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90199-05-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,9 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90199-05:
(7*9)+(6*0)+(5*1)+(4*9)+(3*9)+(2*0)+(1*5)=136
136 % 10 = 6
So 90199-05-6 is a valid CAS Registry Number.

90199-05-6Downstream Products

90199-05-6Relevant articles and documents

Method for synthesizing functionalized 1,3-butadiene based on biomass chemicals

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Page/Page column 0207-0209, (2019/04/26)

The invention provides a method for synthesizing functionalized 1,3-butadiene based on biomass chemicals. The method includes the following steps that under the effect of a condensation catalyst, acetone and a furfural compound are subjected to a condensation reaction, and then a condensation product is obtained; the furfural compound comprises furfural or derivatives of the furfural; then under the effect of a reduction catalyst, the condensation product obtained in the step is subjected to a reduction reaction, and then a reduction product is obtained; under the effect of a catalyst, the reduction product obtained in the step is subjected to a dehydration reaction, and then the functionalized 1,3-butadiene is obtained. According to the method, the acetone and the furfural compound whichare low in cost and easily obtained can be used as raw materials, the functionalized 1,3-butadiene is compounded, experiment conditions are mild, operation is easy, and the method has large-scale synthetic prospects.

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