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CAS

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1377574-60-1

2-((E)-1,3-diphenylallyl)-3-ethyl-1H-indene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1377574-60-1 Structure

  • Basic information

    1. Product Name: 2-((E)-1,3-diphenylallyl)-3-ethyl-1H-indene
    2. Synonyms: 2-((E)-1,3-diphenylallyl)-3-ethyl-1H-indene
    3. CAS NO:1377574-60-1
    4. Molecular Formula:
    5. Molecular Weight: 336.477
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1377574-60-1.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: 2-((E)-1,3-diphenylallyl)-3-ethyl-1H-indene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-((E)-1,3-diphenylallyl)-3-ethyl-1H-indene(1377574-60-1)
    11. EPA Substance Registry System: 2-((E)-1,3-diphenylallyl)-3-ethyl-1H-indene(1377574-60-1)

  • 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: 1377574-60-1(Hazardous Substances Data)

1377574-60-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1377574-60-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,7,5,7 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1377574-60:
(9*1)+(8*3)+(7*7)+(6*7)+(5*5)+(4*7)+(3*4)+(2*6)+(1*0)=201
201 % 10 = 1
So 1377574-60-1 is a valid CAS Registry Number.

1377574-60-1Downstream Products

1377574-60-1Relevant articles and documents

A Gold(I)-Catalyzed Domino Coupling of Alcohols with Allenes Enables the Synthesis of Highly Substituted Indenes

Preinfalk, Alexander,Misale, Antonio,Maulide, Nuno

, p. 14471 - 14474 (2016)

The reaction of aryl-substituted allenes with alcohols under gold catalysis led to highly substituted indenes in good yields, with low catalyst loading and under mild conditions. During this domino transformation, two C?C bonds are formed with water as the only byproduct.

Carbon-carbon bond formation via the electrophilic addition of carbocations to allenes

Meng, Bo,Ma, Shengming

supporting information; experimental part, p. 2674 - 2677 (2012/07/14)

A novel electrophilic addition of aryl-substituted allenes and carbocations forming a carbon-carbon bond is described. Stereodefined allylic halides and indenes were furnished with excellent regio- and stereoselectivity depending on the structure of allenes.

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