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5-broMo-3-((S)-1-Methylpyrrolidin-3-yl)-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1266317-80-9 Structure
  • Basic information

    1. Product Name: 5-broMo-3-((S)-1-Methylpyrrolidin-3-yl)-1H-indole
    2. Synonyms: 5-broMo-3-((S)-1-Methylpyrrolidin-3-yl)-1H-indole
    3. CAS NO:1266317-80-9
    4. Molecular Formula: C13H15BrN2
    5. Molecular Weight: 279.1756
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1266317-80-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-broMo-3-((S)-1-Methylpyrrolidin-3-yl)-1H-indole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-broMo-3-((S)-1-Methylpyrrolidin-3-yl)-1H-indole(1266317-80-9)
    11. EPA Substance Registry System: 5-broMo-3-((S)-1-Methylpyrrolidin-3-yl)-1H-indole(1266317-80-9)
  • 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: 1266317-80-9(Hazardous Substances Data)

1266317-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1266317-80-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,6,3,1 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1266317-80:
(9*1)+(8*2)+(7*6)+(6*6)+(5*3)+(4*1)+(3*7)+(2*8)+(1*0)=159
159 % 10 = 9
So 1266317-80-9 is a valid CAS Registry Number.

1266317-80-9Downstream Products

1266317-80-9Relevant articles and documents

Enantioselective synthesis of 3-substituted tryptamines as core components of central nervous system drugs and indole natural products

Hanessian, Stephen,Stoffman, Elia J.L.

, p. 13 - 20 (2013/03/13)

Application of the MacMillan iminium ion Michael and Friedel-Crafts type reactions to γ-amino α,β-unsaturated butanals led to the corresponding β-substituted butanals in good yields and high enantioselectivities. The products could be useful intermediates

Applications of organocatalytic asymmetric synthesis to drug prototypes-dual action and selective inhibitors of n -nitric oxide synthase with activity against the 5-HT1D/1B subreceptors

Hanessian, Stephen,Stoffman, Eli,Mi, Xueling,Renton, Paul

scheme or table, p. 840 - 843 (2011/04/27)

The scope of MacMillan's organocatalytic asymmetric conjugate addition reaction of indoles and electron-rich aromatics to α,β-unsaturated aldehydes has been extended to the use of 3-amino crotonaldehydes as substrates. The aromatics used include indoles a

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