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(E)-methyl 3-(2-fluorophenyl)-2-((3-methyl-1H-indol-1-yl)methyl)acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1609258-03-8 Structure
  • Basic information

    1. Product Name: (E)-methyl 3-(2-fluorophenyl)-2-((3-methyl-1H-indol-1-yl)methyl)acrylate
    2. Synonyms: (E)-methyl 3-(2-fluorophenyl)-2-((3-methyl-1H-indol-1-yl)methyl)acrylate
    3. CAS NO:1609258-03-8
    4. Molecular Formula:
    5. Molecular Weight: 323.367
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1609258-03-8.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: (E)-methyl 3-(2-fluorophenyl)-2-((3-methyl-1H-indol-1-yl)methyl)acrylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-methyl 3-(2-fluorophenyl)-2-((3-methyl-1H-indol-1-yl)methyl)acrylate(1609258-03-8)
    11. EPA Substance Registry System: (E)-methyl 3-(2-fluorophenyl)-2-((3-methyl-1H-indol-1-yl)methyl)acrylate(1609258-03-8)
  • 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: 1609258-03-8(Hazardous Substances Data)

1609258-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1609258-03-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,2,5 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1609258-03:
(9*1)+(8*6)+(7*0)+(6*9)+(5*2)+(4*5)+(3*8)+(2*0)+(1*3)=168
168 % 10 = 8
So 1609258-03-8 is a valid CAS Registry Number.

1609258-03-8Upstream product

1609258-03-8Relevant articles and documents

Microwave-assisted facile synthesis of [a]-annelated pyrazolopyrroloindoles via intramolecular azomethine imine 1,3-dipolar cycloaddition

Shinde, Anand H.,Vidyacharan, Shinde,Sharada, Duddu S.

, p. 3064 - 3069 (2014)

The synthesis of [a]-annelated pyrazolopyrroloindoles via intramolecular 1,3-dipolar cycloaddition of in situ generated azomethine imine from N-allylated indole-2-carboxaldehyde, in regio- and stereoselective manner by using microwave irradiation is described. A one-pot strategy for the expedient synthesis of pyrazolopyrroloindoles has been developed.

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