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62358-78-5

7-Methoxy-5-methyl-1-indanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 62358-78-5 Structure

  • Basic information

    1. Product Name: 7-Methoxy-5-methyl-1-indanone
    2. Synonyms: 7-Methoxy-5-methylindan-1-one;7-Methoxy-5-methyl-2,3-dihydroindene-1-one;
    3. CAS NO:62358-78-5
    4. Molecular Formula: C11H12O2
    5. Molecular Weight: 176.215
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 62358-78-5.mol

  • Chemical Properties

    1. Melting Point: 133 oC
    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: 7-Methoxy-5-methyl-1-indanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-Methoxy-5-methyl-1-indanone(62358-78-5)
    11. EPA Substance Registry System: 7-Methoxy-5-methyl-1-indanone(62358-78-5)

  • 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: 62358-78-5(Hazardous Substances Data)

62358-78-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62358-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,5 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62358-78:
(7*6)+(6*2)+(5*3)+(4*5)+(3*8)+(2*7)+(1*8)=135
135 % 10 = 5
So 62358-78-5 is a valid CAS Registry Number.

62358-78-5Downstream Products

62358-78-5Relevant articles and documents

The power of solvent in altering the course of photorearrangements

Sebej, Peter,Lim, Bum Hee,Park, Bong Ser,Givens, Richard S.,Klan, Petr

, p. 644 - 647 (2011/04/15)

A clean bifurcation between two important photochemical reactions through competition of a triplet state Type II H-abstraction reaction with a photo-Favorskii rearrangement for (o/p)-hydroxy-o-methylphenacyl esters that depends on the water content of the solvent has been established. The switch from the anhydrous Type II pathway that yields indanones to the aqueous-dependent pathway producing benzofuranones occurs abruptly at low water concentrations (～8%). The surprisingly clean yields suggest that such reactions are synthetically promising.

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