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3-(4-methoxybenzyl)-1H-pyrrolo[3,2-b]pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1060718-09-3 Structure
  • Basic information

    1. Product Name: 3-(4-methoxybenzyl)-1H-pyrrolo[3,2-b]pyridine
    2. Synonyms: 3-(4-methoxybenzyl)-1H-pyrrolo[3,2-b]pyridine
    3. CAS NO:1060718-09-3
    4. Molecular Formula:
    5. Molecular Weight: 238.289
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1060718-09-3.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: 3-(4-methoxybenzyl)-1H-pyrrolo[3,2-b]pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-methoxybenzyl)-1H-pyrrolo[3,2-b]pyridine(1060718-09-3)
    11. EPA Substance Registry System: 3-(4-methoxybenzyl)-1H-pyrrolo[3,2-b]pyridine(1060718-09-3)
  • 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: 1060718-09-3(Hazardous Substances Data)

1060718-09-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1060718-09-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,0,7,1 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1060718-09:
(9*1)+(8*0)+(7*6)+(6*0)+(5*7)+(4*1)+(3*8)+(2*0)+(1*9)=123
123 % 10 = 3
So 1060718-09-3 is a valid CAS Registry Number.

1060718-09-3Downstream Products

1060718-09-3Relevant articles and documents

Synthesis of C3-substituted 4-azaindoles: An easy access to 4-azamelatonin and protected 4-azatryptophan

Jeanty, Matthieu,Suzenet, Franck,Guillaumet, Gerald

, p. 7390 - 7393 (2008)

(Chemical Equation Presented) C3-Substituted-4-azaindoles were synthesized from pyridylacetonitriles in a two-step sequence allowing the easy introduction of a range of substituents. This strategy permits the rapid synthesis of 4-azamelatonin and a protec

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