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1241961-97-6

C27H28N2O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1241961-97-6 Structure

  • Basic information

    1. Product Name: C27H28N2O3
    2. Synonyms:
    3. CAS NO:1241961-97-6
    4. Molecular Formula:
    5. Molecular Weight: 428.531
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1241961-97-6.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: C27H28N2O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C27H28N2O3(1241961-97-6)
    11. EPA Substance Registry System: C27H28N2O3(1241961-97-6)

  • 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: 1241961-97-6(Hazardous Substances Data)

1241961-97-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1241961-97-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,1,9,6 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1241961-97:
(9*1)+(8*2)+(7*4)+(6*1)+(5*9)+(4*6)+(3*1)+(2*9)+(1*7)=156
156 % 10 = 6
So 1241961-97-6 is a valid CAS Registry Number.

1241961-97-6Downstream Products

1241961-97-6Relevant articles and documents

Hexahydropyrrolo [2,3-b]indoles: A new class of structurally rigid tricyclic skeleton for oxazaborolidine-catalyzed asymmetric borane reduction

Xiao, Jian,Wong, Zhen Zhou,Lu, Yun Peng,Loh, Teck Peng

, p. 1107 - 1112 (2010)

A new class of structurally rigid tricyclic chiral ligands based on the hexahydropyrrolo [2,3b]indole skeleton has been rationally designed and the catalytic abilities in asymmetric catalysis have been shown in the enantioselective borane reduction of prochiral ketones to afford the chiral alcohols in excellent yields and high enantioselectivities (up to 97% ee).

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