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1610337-95-5

(E)-benzyl 3-(1-(2-aminophenyl)-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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  • (E)-benzyl 3-(1-(2-aminophenyl)-1H-indol-2-yl)acrylate

    Cas No: 1610337-95-5

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  • 1610337-95-5 Structure

  • Basic information

    1. Product Name: (E)-benzyl 3-(1-(2-aminophenyl)-1H-indol-2-yl)acrylate
    2. Synonyms: (E)-benzyl 3-(1-(2-aminophenyl)-1H-indol-2-yl)acrylate
    3. CAS NO:1610337-95-5
    4. Molecular Formula:
    5. Molecular Weight: 368.435
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1610337-95-5.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: (E)-benzyl 3-(1-(2-aminophenyl)-1H-indol-2-yl)acrylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-benzyl 3-(1-(2-aminophenyl)-1H-indol-2-yl)acrylate(1610337-95-5)
    11. EPA Substance Registry System: (E)-benzyl 3-(1-(2-aminophenyl)-1H-indol-2-yl)acrylate(1610337-95-5)

  • 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: 1610337-95-5(Hazardous Substances Data)

1610337-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1610337-95-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,0,3,3 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1610337-95:
(9*1)+(8*6)+(7*1)+(6*0)+(5*3)+(4*3)+(3*7)+(2*9)+(1*5)=135
135 % 10 = 5
So 1610337-95-5 is a valid CAS Registry Number.

1610337-95-5Downstream Products

1610337-95-5Relevant articles and documents

Rhodium(III)-catalyzed direct C-2 olefination of unactivated indoles utilizing OH/NH2 as directing group

Tang, Chen-Yu,Tao, Yuan,Wu, Xin-Yan,Sha, Feng

, p. 609 - 615 (2014)

Oxidative C-2 olefination of indoles/pyrrole via rhodium(III)-catalyzed direct C-H bond activation is reported. Phenolic OH and aniline NH2 units were revealed to be effective chelating groups to activate the aryl C-H bond. The reactions proceeded with ex

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