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CAS

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1264995-10-9

(-)-ethyl (R)-2-(1-benzyl-2-methyl-1H-indol-3-yl)hexanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1264995-10-9 Structure

  • Basic information

    1. Product Name: (-)-ethyl (R)-2-(1-benzyl-2-methyl-1H-indol-3-yl)hexanoate
    2. Synonyms: (-)-ethyl (R)-2-(1-benzyl-2-methyl-1H-indol-3-yl)hexanoate
    3. CAS NO:1264995-10-9
    4. Molecular Formula:
    5. Molecular Weight: 363.5
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1264995-10-9.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: (-)-ethyl (R)-2-(1-benzyl-2-methyl-1H-indol-3-yl)hexanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (-)-ethyl (R)-2-(1-benzyl-2-methyl-1H-indol-3-yl)hexanoate(1264995-10-9)
    11. EPA Substance Registry System: (-)-ethyl (R)-2-(1-benzyl-2-methyl-1H-indol-3-yl)hexanoate(1264995-10-9)

  • 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: 1264995-10-9(Hazardous Substances Data)

1264995-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1264995-10-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,4,9,9 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1264995-10:
(9*1)+(8*2)+(7*6)+(6*4)+(5*9)+(4*9)+(3*5)+(2*1)+(1*0)=189
189 % 10 = 9
So 1264995-10-9 is a valid CAS Registry Number.

1264995-10-9Downstream Products

1264995-10-9Relevant articles and documents

Rhodium(II)-catalyzed enantioselective C-H functionalization of indoles

Deangelis, Andrew,Shurtleff, Valerie W.,Dmitrenko, Olga,Fox, Joseph M.

supporting information; experimental part, p. 1650 - 1653 (2011/04/17)

A catalytic, enantioselective method for the C-H functionalization of indoles by diazo compounds has been achieved. With catalytic amounts of Rh 2(S-NTTL)4, the putative Rh-carbene intermediates from α-alkyl-α-diazoesters react with indoles at C(3) to provide α-alkyl-α-indolylacetates in high yield and enantioselectivity. From DFT calculations, a mechanism is proposed that involves a Rh-ylide intermediate with oxocarbenium character.

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