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109391-44-8

C30H46O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 109391-44-8 Structure

  • Basic information

    1. Product Name: C30H46O2
    2. Synonyms: C30H46O2
    3. CAS NO:109391-44-8
    4. Molecular Formula:
    5. Molecular Weight: 438.694
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 109391-44-8.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: C30H46O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C30H46O2(109391-44-8)
    11. EPA Substance Registry System: C30H46O2(109391-44-8)

  • 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: 109391-44-8(Hazardous Substances Data)

109391-44-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109391-44-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,3,9 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 109391-44:
(8*1)+(7*0)+(6*9)+(5*3)+(4*9)+(3*1)+(2*4)+(1*4)=128
128 % 10 = 8
So 109391-44-8 is a valid CAS Registry Number.

109391-44-8Upstream product

109391-44-8Downstream Products

109391-44-8Relevant articles and documents

Alkali ion exchanged nafion as a confining medium for photochemical reactions

Arumugam, Selvanathan,Kaanumalle, Lakshmi S.,Ramamurthy

, p. 139 - 145 (2006)

Methanol-swollen Nafion beads were used as microreactors to control the photochemical reaction pathways. Product selectivity in three unimolecular reactions, namely, the photo-Fries rearrangement of naphthyl esters, Norrish Type I reaction of 1-phenyl-3-p-tolyl-propan-2-one and Norrish Type I and Type II reactions of benzoin alkyl ethers were examined. The influence of cations over the photodimerization of acenaphthylene and cross-photodimerization between acenaphthylene and N-benzyl maleimide included within Nafion were also examined. The photochemical behaviors of the above substrates were significantly altered within Nafion compared with their solution photochemistry. Of particular interest, the product distributions were found to depend on the counter cations of Nafion.

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