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1273331-68-2

C25H23BrN2O4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1273331-68-2 Structure

  • Basic information

    1. Product Name: C25H23BrN2O4
    2. Synonyms:
    3. CAS NO:1273331-68-2
    4. Molecular Formula:
    5. Molecular Weight: 495.373
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1273331-68-2.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: C25H23BrN2O4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C25H23BrN2O4(1273331-68-2)
    11. EPA Substance Registry System: C25H23BrN2O4(1273331-68-2)

  • 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: 1273331-68-2(Hazardous Substances Data)

1273331-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1273331-68-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,3,3,3 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1273331-68:
(9*1)+(8*2)+(7*7)+(6*3)+(5*3)+(4*3)+(3*1)+(2*6)+(1*8)=142
142 % 10 = 2
So 1273331-68-2 is a valid CAS Registry Number.

1273331-68-2Downstream Products

1273331-68-2Relevant articles and documents

Dynamic kinetic asymmetric synthesis of five contiguous stereogenic centers by sequential organocatalytic stetter and Michael-Aldol reaction: Enantioselective synthesis of fully substituted cyclopentanols bearing a quaternary stereocenter

Hong, Bor-Cherng,Dange, Nitin S.,Hsu, Che-Sheng,Liao, Ju-Hsiou,Lee, Gene-Hsiang

supporting information; experimental part, p. 1338 - 1341 (2011/05/08)

A synthesis of fully substituted cyclopentanes bearing a quaternary carbon center and five contiguous stereogenic centers has been achieved by sequential organocatalyzed Stetter and Michael-Aldol reactions of heteroaromatic aldehydes, nitroalkenes, and α,

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