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CAS

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849360-69-6

(-)-3a-methylfuroindoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 849360-69-6 Structure

  • Basic information

    1. Product Name: (-)-3a-methylfuroindoline
    2. Synonyms: (-)-3a-methylfuroindoline
    3. CAS NO:849360-69-6
    4. Molecular Formula:
    5. Molecular Weight: 309.365
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 849360-69-6.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: (-)-3a-methylfuroindoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: (-)-3a-methylfuroindoline(849360-69-6)
    11. EPA Substance Registry System: (-)-3a-methylfuroindoline(849360-69-6)

  • 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: 849360-69-6(Hazardous Substances Data)

849360-69-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 849360-69-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,3,6 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 849360-69:
(8*8)+(7*4)+(6*9)+(5*3)+(4*6)+(3*0)+(2*6)+(1*9)=206
206 % 10 = 6
So 849360-69-6 is a valid CAS Registry Number.

849360-69-6Relevant articles and documents

Total synthesis of (-)-physovenine from (-)-3a-hydroxyfuroindoline

Sunazuka, Toshiaki,Yoshida, Kiminari,Kojima, Naoto,Shirahata, Tatsuya,Hirose, Tomoyasu,Handa, Masaki,Yamamoto, Daisuke,Harigaya, Yoshihiro,Kuwajima, Isao,Omura, Satoshi

, p. 1459 - 1461 (2007/10/03)

Total synthesis of calabar bean alkaloid (-)-physovenine (-)-3 has been achieved in a concise manner starting from optically active (-)-3a- hydroxyfuroindoline (-)-2, synthesized via modified Sharpless epoxidation of tryptophol 1. Our strategy involved a

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