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CAS

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183728-64-5

Bicyclo[2.2.2]oct-2-ene-2-carboxylic acid, 1-(methoxyphenylmethoxy)-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 183728-64-5 Structure

  • Basic information

    1. Product Name: Bicyclo[2.2.2]oct-2-ene-2-carboxylic acid, 1-(methoxyphenylmethoxy)-4-methyl-
    2. Synonyms:
    3. CAS NO:183728-64-5
    4. Molecular Formula: C18H22O4
    5. Molecular Weight: 302.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 183728-64-5.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: Bicyclo[2.2.2]oct-2-ene-2-carboxylic acid, 1-(methoxyphenylmethoxy)-4-methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Bicyclo[2.2.2]oct-2-ene-2-carboxylic acid, 1-(methoxyphenylmethoxy)-4-methyl-(183728-64-5)
    11. EPA Substance Registry System: Bicyclo[2.2.2]oct-2-ene-2-carboxylic acid, 1-(methoxyphenylmethoxy)-4-methyl-(183728-64-5)

  • 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: 183728-64-5(Hazardous Substances Data)

183728-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183728-64-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,7,2 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 183728-64:
(8*1)+(7*8)+(6*3)+(5*7)+(4*2)+(3*8)+(2*6)+(1*4)=165
165 % 10 = 5
So 183728-64-5 is a valid CAS Registry Number.

183728-64-5Downstream Products

183728-64-5Relevant articles and documents

Efficient intramolecular general acid catalysis of the hydrolysis of a dialkyl acetal

Brown, Christopher J.,Kirby, Anthony J.

, p. 2355 - 2356 (1996)

The hydrolysis of benzaldehyde acetal 3, catalysed by the neighbouring carboxy group, is some 105 times faster than that of a comparable system 6, which does not form a strong intramolecular hydrogen bond in the transition state for the reaction.

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