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CAS

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132903-60-7

Bicyclo[4.1.0]heptane-1-carboxylic acid, methyl ester, (-)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132903-60-7 Structure

  • Basic information

    1. Product Name: Bicyclo[4.1.0]heptane-1-carboxylic acid, methyl ester, (-)- (9CI)
    2. Synonyms: Bicyclo[4.1.0]heptane-1-carboxylic acid, methyl ester, (-)- (9CI)
    3. CAS NO:132903-60-7
    4. Molecular Formula: C9H14O2
    5. Molecular Weight: 154.20626
    6. EINECS: N/A
    7. Product Categories: CARBOXYLICESTER
    8. Mol File: 132903-60-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 190.4±8.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.120±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Bicyclo[4.1.0]heptane-1-carboxylic acid, methyl ester, (-)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Bicyclo[4.1.0]heptane-1-carboxylic acid, methyl ester, (-)- (9CI)(132903-60-7)
    11. EPA Substance Registry System: Bicyclo[4.1.0]heptane-1-carboxylic acid, methyl ester, (-)- (9CI)(132903-60-7)

  • 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: 132903-60-7(Hazardous Substances Data)

132903-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132903-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,9,0 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132903-60:
(8*1)+(7*3)+(6*2)+(5*9)+(4*0)+(3*3)+(2*6)+(1*0)=107
107 % 10 = 7
So 132903-60-7 is a valid CAS Registry Number.

132903-60-7Downstream Products

132903-60-7Relevant articles and documents

Substituent Effects on Hydrogenation of Aromatic Rings: Hydrogenation vs. Hydrogenolysis in Cyclic Analogues of Benzyl Ethers.

Anzalone, Luigi,Hirsch, Jerry A.

, p. 2128 - 2133 (2007/10/02)

Carbalkoxy substituents are shown to retard the hydrogenation of aromatic rings over Rh/C catalyst.Hydrogenolysis predominates with acyclic (benzyloxy)acetates over this catalyst, but both hydrogenation and hydrogenolysis become sluggish with 2-isochroman-4-ones (1).However, phthalides may be cleanly hydrogenated in moderate to excellent yields without significant hydrogenolysis.Placing a benzyl ether in a ring system appears to greatly retard hydrogenolysis relative to the acyclic analogues.

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