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1526987-34-7

C26H26NO3P is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1526987-34-7 Structure

  • Basic information

    1. Product Name: C26H26NO3P
    2. Synonyms: C26H26NO3P
    3. CAS NO:1526987-34-7
    4. Molecular Formula:
    5. Molecular Weight: 431.471
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1526987-34-7.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: C26H26NO3P(CAS DataBase Reference)
    10. NIST Chemistry Reference: C26H26NO3P(1526987-34-7)
    11. EPA Substance Registry System: C26H26NO3P(1526987-34-7)

  • 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: 1526987-34-7(Hazardous Substances Data)

1526987-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1526987-34-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,2,6,9,8 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1526987-34:
(9*1)+(8*5)+(7*2)+(6*6)+(5*9)+(4*8)+(3*7)+(2*3)+(1*4)=207
207 % 10 = 7
So 1526987-34-7 is a valid CAS Registry Number.

1526987-34-7Downstream Products

1526987-34-7Relevant articles and documents

An expedient synthesis of pyrrole-2-phosphonates via direct oxidative phosphorylation and γ-hydroxy-γ-butyrolactams from pyrroles

Kim, Se Hee,Kim, Ko Hoon,Lim, Jin Woo,Kim, Jae Nyoung

, p. 531 - 534 (2014)

An expedient oxidative phosphorylation of pyrroles has been disclosed. The reaction of dialkyl phosphite and pyrrole in the presence of AgNO 3/K2S2O8 in DMF/H2O (8:1) produced pyrrole-2-phosphonates in good yields. In the absence of dialkyl phosphite, γ-hydroxy-γ-butyrolactam derivative was formed as a major product.

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