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1373884-02-6

2-iodo-7-methoxy-4-methyl-3-phenyl-4H-spiro[cyclopenta-[b]indole-1,9′-fluorene] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1373884-02-6 Structure

  • Basic information

    1. Product Name: 2-iodo-7-methoxy-4-methyl-3-phenyl-4H-spiro[cyclopenta-[b]indole-1,9′-fluorene]
    2. Synonyms:
    3. CAS NO:1373884-02-6
    4. Molecular Formula:
    5. Molecular Weight: 551.426
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1373884-02-6.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: 2-iodo-7-methoxy-4-methyl-3-phenyl-4H-spiro[cyclopenta-[b]indole-1,9′-fluorene](CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-iodo-7-methoxy-4-methyl-3-phenyl-4H-spiro[cyclopenta-[b]indole-1,9′-fluorene](1373884-02-6)
    11. EPA Substance Registry System: 2-iodo-7-methoxy-4-methyl-3-phenyl-4H-spiro[cyclopenta-[b]indole-1,9′-fluorene](1373884-02-6)

  • 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: 1373884-02-6(Hazardous Substances Data)

1373884-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1373884-02-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,8,8 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1373884-02:
(9*1)+(8*3)+(7*7)+(6*3)+(5*8)+(4*8)+(3*4)+(2*0)+(1*2)=186
186 % 10 = 6
So 1373884-02-6 is a valid CAS Registry Number.

1373884-02-6Downstream Products

1373884-02-6Relevant articles and documents

3-alkenylation or 3-alkylation of indole with propargylic alcohols: Construction of 3,4-dihydrocyclopenta[ b ]indole and 1,4-dihydrocyclopenta[ b ]indole in the presence of different catalysts

Zhang, Li,Zhu, Yuanxun,Yin, Guangwei,Lu, Ping,Wang, Yanguang

, p. 9510 - 9520 (2012)

3-Alkenylation or 3-alkylation of indole with propargylic alcohols could be efficiently controlled by the catalyst. In the presence of triflic acid, 3-alkenylation of indole occurred and a 3,4-dihydrocyclopenta[b]indole skeleton was effectively constructed in moderate to excellent yields via a cascade process. In the presence of Cu(OTf)2, 3-alkylation of indole resulted in the formation of 3-propargylic indole, which could be further converted into 2-iodo-1,4-dihydrocyclopenta[b]indoles in the presence of N-iodosuccinimide and boron trifluoride etherate. Possible mechanisms related to the 3-alkenylation or 3-alkylation of indole and their extension to the formation of 3,4-dihydrocyclopenta[b]indoles or 1,4-dihydrocyclopenta[b]indoles are postulated and discussed.

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