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CAS

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137725-05-4

2-Butenamide, 4-cyclohexylidene-4-(2-methoxyphenoxy)-N,N-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 137725-05-4 Structure

  • Basic information

    1. Product Name: 2-Butenamide, 4-cyclohexylidene-4-(2-methoxyphenoxy)-N,N-dimethyl-
    2. Synonyms:
    3. CAS NO:137725-05-4
    4. Molecular Formula: C19H25NO3
    5. Molecular Weight: 315.412
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 137725-05-4.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: 2-Butenamide, 4-cyclohexylidene-4-(2-methoxyphenoxy)-N,N-dimethyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Butenamide, 4-cyclohexylidene-4-(2-methoxyphenoxy)-N,N-dimethyl-(137725-05-4)
    11. EPA Substance Registry System: 2-Butenamide, 4-cyclohexylidene-4-(2-methoxyphenoxy)-N,N-dimethyl-(137725-05-4)

  • 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: 137725-05-4(Hazardous Substances Data)

137725-05-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137725-05-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,7,2 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 137725-05:
(8*1)+(7*3)+(6*7)+(5*7)+(4*2)+(3*5)+(2*0)+(1*5)=134
134 % 10 = 4
So 137725-05-4 is a valid CAS Registry Number.

137725-05-4Downstream Products

137725-05-4Relevant articles and documents

Synthesis of 1,3-dienes bearing both electron-donor and acceptor substituents

Moreau,Al Neirabeyeh,Guillaumet,Coudert

, p. 5525 - 5528 (2007/10/02)

Allylic benzodioxinic alcohols were prepared from 1,4-benzodioxin and then submitted to the orhoester Claisen rearrangement and Eschenmoser procedure leading to 3-substituted-2-alkylidene-1,4-benzodioxans. Di-and trisubstituted 1,3-dienes bearing both electron-donor and acceptor substituents were obtained in good yields from these compounds.

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