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CAS

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102148-88-9

ethyl octyl phthalate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 102148-88-9 Structure

  • Basic information

    1. Product Name: ethyl octyl phthalate
    2. Synonyms: ethyl octyl phthalate
    3. CAS NO:102148-88-9
    4. Molecular Formula:
    5. Molecular Weight: 306.402
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102148-88-9.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 octyl phthalate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl octyl phthalate(102148-88-9)
    11. EPA Substance Registry System: ethyl octyl phthalate(102148-88-9)

  • 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: 102148-88-9(Hazardous Substances Data)

102148-88-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102148-88-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,1,4 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 102148-88:
(8*1)+(7*0)+(6*2)+(5*1)+(4*4)+(3*8)+(2*8)+(1*8)=89
89 % 10 = 9
So 102148-88-9 is a valid CAS Registry Number.

102148-88-9Downstream Products

102148-88-9Relevant articles and documents

Mucor miehei lipase catalyzed transesterifications on aromatic and heteroaromatic substrates. A general survey

Martin-Munoz, Maria Gema,Fierros, Maria,Rodriguez-Franco, Maria Isabel,Conde, Santiago

, p. 6999 - 7008 (1994)

An investigation on Mucor miehei lipase-catalyzed transesterifications of 16 aromatic and heteroaromatic esters in organic solvents is described. The points studied were the activity and regioselectivity of the enzyme-catalyzed reaction of either one or two ester groups situated in different positions on several heterocyclic systems with an aliphatic alcohol. The reactions took place in moderate to good yields and, in some cases, regioselectively.

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