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125117-25-1

ethyl 1-cyano-2-carbomethoxycyclopropanecarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 125117-25-1 Structure

  • Basic information

    1. Product Name: ethyl 1-cyano-2-carbomethoxycyclopropanecarboxylate
    2. Synonyms: ethyl 1-cyano-2-carbomethoxycyclopropanecarboxylate
    3. CAS NO:125117-25-1
    4. Molecular Formula:
    5. Molecular Weight: 197.191
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 125117-25-1.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: ethyl 1-cyano-2-carbomethoxycyclopropanecarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 1-cyano-2-carbomethoxycyclopropanecarboxylate(125117-25-1)
    11. EPA Substance Registry System: ethyl 1-cyano-2-carbomethoxycyclopropanecarboxylate(125117-25-1)

  • 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: 125117-25-1(Hazardous Substances Data)

125117-25-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125117-25-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,1,1 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 125117-25:
(8*1)+(7*2)+(6*5)+(5*1)+(4*1)+(3*7)+(2*2)+(1*5)=91
91 % 10 = 1
So 125117-25-1 is a valid CAS Registry Number.

125117-25-1Downstream Products

125117-25-1Relevant articles and documents

TRIBUTYLSTIBINE MEDIATED SYNTHESIS OF 1,1,2-TRI-SUBSTITUTED CYCLOPROPANES

Chen, Chen,Liao, Yi,Huang, Yao-Zeng

, p. 3011 - 3020 (2007/10/02)

A novel method for the synthesis of 1,1,2-tri-substituted cyclopropanes is reported which involves the reaction of electron-deficient olefins with dibromomalonic ester, dibromocyanoacetic or dibromobenzeneacetic ester promoted by tri-n-butylstibine.The reaction was carried out under mild conditions to give the cyclopropane derivatives in moderate to good yields.Other R3M (M= As,Sb,Bi) reagents as promoter for this reaction have been studied and seem to be less effective than tributylstibine.

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