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  • 245664-92-0 Structure
  • Basic information

    1. Product Name: C71H13NO2
    2. Synonyms:
    3. CAS NO:245664-92-0
    4. Molecular Formula:
    5. Molecular Weight: 911.89
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 245664-92-0.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: C71H13NO2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C71H13NO2(245664-92-0)
    11. EPA Substance Registry System: C71H13NO2(245664-92-0)
  • 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: 245664-92-0(Hazardous Substances Data)

245664-92-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 245664-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,5,6,6 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 245664-92:
(8*2)+(7*4)+(6*5)+(5*6)+(4*6)+(3*4)+(2*9)+(1*2)=160
160 % 10 = 0
So 245664-92-0 is a valid CAS Registry Number.

245664-92-0Downstream Products

245664-92-0Relevant articles and documents

Study on the thermal reactions of [60]fullerene with amino acids and amino acid esters

Zhu, San-E,Cheng, Xin,Li, Yu-Jin,Mai, Cheng-Kang,Huang, Yong-Shun,Wang, Guan-Wu,Peng, Ru-Fang,Jin, Bo,Chu, Shi-Jin

, p. 8720 - 8729 (2012)

Thermal reactions of [60]fullerene with a series of amino acids and amino acid esters under aerobic and dark conditions have been investigated. Fulleropyrrolidines can be obtained from these reactions although an aldehyde is not added purposely. Possible reaction mechanisms involving uncommon C-N bond cleavages have been proposed to generate aldehydes, which then react with amino acids and amino acid esters to provide azomethine ylides, followed by 1,3-dipolar cycloaddition to [60]fullerene affording fulleropyrrolidines. Control experiments support our proposed mechanisms, and elucidate the innate nature of C-N bond cleavages of amino acids and amino acid esters.

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