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CAS

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1384442-33-4

C14H14BrNO3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1384442-33-4 Structure

  • Basic information

    1. Product Name: C14H14BrNO3
    2. Synonyms: C14H14BrNO3
    3. CAS NO:1384442-33-4
    4. Molecular Formula:
    5. Molecular Weight: 324.174
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1384442-33-4.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: C14H14BrNO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H14BrNO3(1384442-33-4)
    11. EPA Substance Registry System: C14H14BrNO3(1384442-33-4)

  • 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: 1384442-33-4(Hazardous Substances Data)

1384442-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1384442-33-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,4,4 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1384442-33:
(9*1)+(8*3)+(7*8)+(6*4)+(5*4)+(4*4)+(3*2)+(2*3)+(1*3)=164
164 % 10 = 4
So 1384442-33-4 is a valid CAS Registry Number.

1384442-33-4Downstream Products

1384442-33-4Relevant articles and documents

Primary 1,2-diamine catalysis (V): Efficient asymmetric aldol reactions of isatins with cyclohexanone

Liu, Yi,Gao, Pengchao,Wang, Junfeng,Sun, Qi,Ge, Zemei,Li, Runtao

, p. 1031 - 1034 (2012)

1,2-Diaminocyclohexane-hexanedioic acid has been demonstrated to catalyze the asymmetric aldol reactions of cycloketones and various isatin derivatives efficiently in MeOH-H. The corresponding products were obtained in good yields (70-90%) with high diastereoselectivity (up to 99:1 anti/syn) and enantioselectivity (up to 99% ee). Georg Thieme Verlag Stuttgart · New York.

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