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92294-81-0

trans-4-Chlor-α-Methyl-zimtsaeure-butylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 92294-81-0 Structure

  • Basic information

    1. Product Name: trans-4-Chlor-α-Methyl-zimtsaeure-butylester
    2. Synonyms:
    3. CAS NO:92294-81-0
    4. Molecular Formula:
    5. Molecular Weight: 252.741
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92294-81-0.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: trans-4-Chlor-α-Methyl-zimtsaeure-butylester(CAS DataBase Reference)
    10. NIST Chemistry Reference: trans-4-Chlor-α-Methyl-zimtsaeure-butylester(92294-81-0)
    11. EPA Substance Registry System: trans-4-Chlor-α-Methyl-zimtsaeure-butylester(92294-81-0)

  • 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: 92294-81-0(Hazardous Substances Data)

92294-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92294-81-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,9 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 92294-81:
(7*9)+(6*2)+(5*2)+(4*9)+(3*4)+(2*8)+(1*1)=150
150 % 10 = 0
So 92294-81-0 is a valid CAS Registry Number.

92294-81-0Downstream Products

92294-81-0Relevant articles and documents

First efficient palladium-catalyzed Heck reactions of aryl bromides with alkyl methacrylate

Beller, Matthias,Riermeier, Thomas H.

, p. 6535 - 6538 (1996)

An efficient palladium-catalyzed coupling reactions of aryl bromides with butyl methacrylate has been developed. Depending on the reaction conditions various amounts of butyl 3-aryl-2-methylpropenoate and butyl 3-aryl-2-methyliden-propenoate as well as do

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