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CAS

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141351-76-0

C35H51NO7 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 141351-76-0 Structure

  • Basic information

    1. Product Name: C35H51NO7
    2. Synonyms: C35H51NO7
    3. CAS NO:141351-76-0
    4. Molecular Formula:
    5. Molecular Weight: 597.792
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 141351-76-0.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: C35H51NO7(CAS DataBase Reference)
    10. NIST Chemistry Reference: C35H51NO7(141351-76-0)
    11. EPA Substance Registry System: C35H51NO7(141351-76-0)

  • 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: 141351-76-0(Hazardous Substances Data)

141351-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141351-76-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,3,5 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 141351-76:
(8*1)+(7*4)+(6*1)+(5*3)+(4*5)+(3*1)+(2*7)+(1*6)=100
100 % 10 = 0
So 141351-76-0 is a valid CAS Registry Number.

141351-76-0Downstream Products

141351-76-0Relevant articles and documents

Studies on cardiac ingredients of plants. IX. Chemical transformation of proscillaridin by utilizing its 1,4-cycloadducts as key compounds and biological activities of their derivatives

Tanase,Murakami,Nagai,Ueda,Sakakibara,Ando,Hotta,Takeya

, p. 327 - 332 (2007/10/02)

Three aromatic compounds (2-4) possessing a carbomethoxyl group or a dimethoxyphthaloyl group, prepared by the Diels-Alder reaction of the cardiac glycoside, proscillaridin (1), with dimethyl acetylenedicarboxylate and methyl propiolate, were transformed

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