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95671-22-0

cis-nemorensic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 95671-22-0 Structure

  • Basic information

    1. Product Name: cis-nemorensic acid
    2. Synonyms:
    3. CAS NO:95671-22-0
    4. Molecular Formula:
    5. Molecular Weight: 216.234
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 95671-22-0.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: cis-nemorensic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: cis-nemorensic acid(95671-22-0)
    11. EPA Substance Registry System: cis-nemorensic acid(95671-22-0)

  • 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: 95671-22-0(Hazardous Substances Data)

95671-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95671-22-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,7 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 95671-22:
(7*9)+(6*5)+(5*6)+(4*7)+(3*1)+(2*2)+(1*2)=160
160 % 10 = 0
So 95671-22-0 is a valid CAS Registry Number.

95671-22-0Downstream Products

95671-22-0Relevant articles and documents

OXYNEMORENSINE, AN ALKALOID FROM Senecio nemorensis L., VAR. subdecurrens GRISEB.

Klasek, Antonin,Sedmera, Petr,Vokoun, Jindrich,Boeva, Anna,Dvorackova, Svatava,Santavy, Frantisek

, p. 548 - 558 (2007/10/02)

From S. nemorensis L., var. subdecurrens GRISEB. there were isolated the previously obtained alkaloids nemorensine (I), retroisosenine (II), bulgarsenine (III) and, in addition, the alkaloid oxynemorensine which was assigned the structure VIII on the basis of the interpretation of the 1H-NMR, 13C-NMR, mass spectra, and on that of the identification of the products of hydrolysis and reduction.Furthemore, the isolation of the cis-nemorensic acid (V) as well as that of the unsaturated acid IV, and the transformation of bulgarsenine (III) to nemorensine (I) were described.

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