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CAS

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1361029-67-5

(Z)-methyl 3-(4-methoxyphenyl)-2-methyl-3-(3-methyl-1H-indol-2-yl)acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1361029-67-5 Structure

  • Basic information

    1. Product Name: (Z)-methyl 3-(4-methoxyphenyl)-2-methyl-3-(3-methyl-1H-indol-2-yl)acrylate
    2. Synonyms:
    3. CAS NO:1361029-67-5
    4. Molecular Formula:
    5. Molecular Weight: 335.403
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1361029-67-5.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: (Z)-methyl 3-(4-methoxyphenyl)-2-methyl-3-(3-methyl-1H-indol-2-yl)acrylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-methyl 3-(4-methoxyphenyl)-2-methyl-3-(3-methyl-1H-indol-2-yl)acrylate(1361029-67-5)
    11. EPA Substance Registry System: (Z)-methyl 3-(4-methoxyphenyl)-2-methyl-3-(3-methyl-1H-indol-2-yl)acrylate(1361029-67-5)

  • 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: 1361029-67-5(Hazardous Substances Data)

1361029-67-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1361029-67-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,1,0,2 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1361029-67:
(9*1)+(8*3)+(7*6)+(6*1)+(5*0)+(4*2)+(3*9)+(2*6)+(1*7)=135
135 % 10 = 5
So 1361029-67-5 is a valid CAS Registry Number.

1361029-67-5Downstream Products

1361029-67-5Relevant articles and documents

Aerobic palladium(II)-catalyzed 5-endo-trig cyclization: An entry into the diastereoselective C-2 alkenylation of indoles with tri- and tetrasubstituted double bonds

Kandukuri, Sandeep R.,Schiffner, Julia A.,Oestreich, Martin

, p. 1265 - 1269 (2012/03/08)

The endo trick: An endo ring closure onto the trigonal β carbon atom of α,β-unsaturated acceptors that are tethered to the indole nitrogen atom followed by amide cleavage enables the diastereoselective C-2 alkenylation of indoles with fully substituted double bonds. The carboxy group functions as a synthetically useful temporary tether (see scheme). Copyright

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