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30745-31-4

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

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  • 30745-31-4 Structure

  • Basic information

    1. Product Name: Cycleanin
    2. Synonyms:
    3. CAS NO:30745-31-4
    4. Molecular Formula:
    5. Molecular Weight: 622.761
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 30745-31-4.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: Cycleanin(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cycleanin(30745-31-4)
    11. EPA Substance Registry System: Cycleanin(30745-31-4)

  • 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: 30745-31-4(Hazardous Substances Data)

30745-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30745-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,4 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30745-31:
(7*3)+(6*0)+(5*7)+(4*4)+(3*5)+(2*3)+(1*1)=94
94 % 10 = 4
So 30745-31-4 is a valid CAS Registry Number.

30745-31-4Relevant articles and documents

Synthesis of cycleanine mono-N-oxides

Kashiwaba,Oho,Toda,Suzuki,Sano

, p. 253 - 255 (1998)

Oxidation of cycleanine (3) with m-chloroperbenzoic acid gave two diastereomeric N-oxides (1 and 2), and their stereochemistry was unambiguously determined on the basis of spectroscopic evidence. The NMR spectra of synthetic cycleanine mono-N-oxides 1 and 2 were significantly different from those of the natural product previously reported to be cycleanine N-oxide.

Alkaloidal constituents of the tubers of Stephania cepharantha cultivated in Japan: Structure of 3,4-dehydrocycleanine, a new bisbenzylisoquinoline alkaloid

Kashiwaba, Noriaki,Morooka, Shigeo,Kimura, Michiko,Murakoshi, Yoshie,Ono, Minoru,Toda, Jun,Suzuki, Hideki,Sano, Takehiro

, p. 470 - 475 (2007/10/03)

Full details of the isolation and characterization of 52 alkaloids obtained from the tubers of Stephania cepharantha Hayata (Menispermaceae) cultivated in Japan are presented, along with the structural determination of a new bisbenzylisoquinoline alkaloid, 3,4-dehydrocycleanine (8).

THE BIOSYNTHESIS OF THE ALKALOIDS OF CISSAMPELOS PAREIRA LINN

Bhakuni,Dewan S.,Jain,Sudha,Chaturvedi,Rekha

, p. 3975 - 3982 (2007/10/02)

Tracer experimets show that the bisbenzylisoqunoline alkaloid,(S,R)-hayatidin (10) is stereospecifically biosynthesized in young Cissampelos pareira Linn plants by intermolecular oxidativ coupling of (S)-(5)-and (R)-(3)-N-methylcoclaurines whereas (R,R)-isochondrodendrine (14) and (R,R)-bebeerine (12) are formed in the plants by oxidative dimerization of (R)-N-methyl-coclaurine (3).

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