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1038610-02-4

diethyl 5-ethoxycarbonyl-6-phenyl-1H-indene-2,2(3H)-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1038610-02-4 Structure

  • Basic information

    1. Product Name: diethyl 5-ethoxycarbonyl-6-phenyl-1H-indene-2,2(3H)-dicarboxylate
    2. Synonyms: diethyl 5-ethoxycarbonyl-6-phenyl-1H-indene-2,2(3H)-dicarboxylate
    3. CAS NO:1038610-02-4
    4. Molecular Formula:
    5. Molecular Weight: 410.467
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1038610-02-4.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: diethyl 5-ethoxycarbonyl-6-phenyl-1H-indene-2,2(3H)-dicarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: diethyl 5-ethoxycarbonyl-6-phenyl-1H-indene-2,2(3H)-dicarboxylate(1038610-02-4)
    11. EPA Substance Registry System: diethyl 5-ethoxycarbonyl-6-phenyl-1H-indene-2,2(3H)-dicarboxylate(1038610-02-4)

  • 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: 1038610-02-4(Hazardous Substances Data)

1038610-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1038610-02-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,8,6,1 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1038610-02:
(9*1)+(8*0)+(7*3)+(6*8)+(5*6)+(4*1)+(3*0)+(2*0)+(1*2)=114
114 % 10 = 4
So 1038610-02-4 is a valid CAS Registry Number.

1038610-02-4Downstream Products

1038610-02-4Relevant articles and documents

RhCl3/amine-catalyzed [2+2+2] cyclization of alkynes

Yoshida, Kenta,Morimoto, Ichiro,Mitsudo, Koichi,Tanaka, Hideo

, p. 5800 - 5807 (2008)

The RhCl3·3H2O/i-Pr2NEt-catalyzed [2+2+2] cyclotrimerization of alkynes has been achieved. The reaction can be widely used for various alkynes and provides tri- or hexa-substituted benzenes regioselectively in high yields. The [2+2+2] cycloaddition of diynes and alkynes is also developed, and it affords benzene derivatives in moderate to high yields.

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