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1017041-20-1

C14H9BrF3NO is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1017041-20-1 Structure

  • Basic information

    1. Product Name: C14H9BrF3NO
    2. Synonyms: C14H9BrF3NO
    3. CAS NO:1017041-20-1
    4. Molecular Formula:
    5. Molecular Weight: 344.131
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1017041-20-1.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: C14H9BrF3NO(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H9BrF3NO(1017041-20-1)
    11. EPA Substance Registry System: C14H9BrF3NO(1017041-20-1)

  • 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: 1017041-20-1(Hazardous Substances Data)

1017041-20-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1017041-20-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,7,0,4 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1017041-20:
(9*1)+(8*0)+(7*1)+(6*7)+(5*0)+(4*4)+(3*1)+(2*2)+(1*0)=81
81 % 10 = 1
So 1017041-20-1 is a valid CAS Registry Number.

1017041-20-1Relevant articles and documents

Pd-Catalyzed Carbonylative Synthesis of 4H-Benzo[d][1,3]Oxazin-4-Ones Using Benzene-1,3,5-Triyl Triformate as the CO Source

Zheng, Yan,Dong, Mengke,Qu, Erdong,Bai, Jin,Wu, Xiao-Feng,Li, Wanfang

supporting information, p. 16219 - 16224 (2021/10/06)

A facile synthesis of 4H-benzo[d][1,3]oxazin-4-one derivatives by Pd-catalyzed carbonylative cross-coupling between N-(ortho-bromoaryl)amides and benzene-1,3,5-triyl triformate (TFBen) was developed. This procedure does not require the toxic and flammable gas CO as the carbonyl source and tolerates a wide scope of functional groups. Remarkably, 4H-benzo[d][1,3]oxazin-4-ones incorporated to natural products and drugs can be constructed by this method.

Photocatalyst- And Transition-Metal-Free Visible-Light-Promoted Intramolecular C(sp2)-S Formation

Wang, Hao,Wu, Qi,Zhang, Jian-Dong,Li, Hai-Yan,Li, Hong-Xi

supporting information, p. 2078 - 2083 (2021/04/05)

A photocatalyst- and transition-metal-free visible-light-induced cyclization of ortho-halothiobenzanilides has been developed. Upon irradiation with visible light, substrates undergo dehalogenative cyclization to 2-aryl benzothiazoles with high efficiency and selectivity. This photocyclization exhibits a high tolerance to various functional groups, is applicable for the synthesis of 2-alkyl benzothiazoles, and is easy to set up for gram-scale reaction.

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