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1429318-81-9

C22H18BrF3N4O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1429318-81-9 Structure

  • Basic information

    1. Product Name: C22H18BrF3N4O3
    2. Synonyms: C22H18BrF3N4O3
    3. CAS NO:1429318-81-9
    4. Molecular Formula:
    5. Molecular Weight: 523.309
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1429318-81-9.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: C22H18BrF3N4O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H18BrF3N4O3(1429318-81-9)
    11. EPA Substance Registry System: C22H18BrF3N4O3(1429318-81-9)

  • 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: 1429318-81-9(Hazardous Substances Data)

1429318-81-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1429318-81-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,9,3,1 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1429318-81:
(9*1)+(8*4)+(7*2)+(6*9)+(5*3)+(4*1)+(3*8)+(2*8)+(1*1)=169
169 % 10 = 9
So 1429318-81-9 is a valid CAS Registry Number.

1429318-81-9Downstream Products

1429318-81-9Relevant articles and documents

Copper-catalyzed diastereoselective arylation of tryptophan derivatives: Total synthesis of (+)-naseseazines A and B

Kieffer, Madeleine E.,Chuang, Kangway V.,Reisman, Sarah E.

supporting information, p. 5557 - 5560 (2013/05/22)

A copper-catalyzed arylation of tryptophan derivatives is reported. The reaction proceeds with high site-and diastereoselectivity to provide aryl pyrroloindoline products in one step from simple starting materials. The utility of this transformation is highlighted in the five-step syntheses of the natural products (+)-naseseazine A and B.

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