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CAS

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1567382-95-9

2-(2,3,5,6-tetrafluorophenyl)benzo[d]oxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1567382-95-9 Structure

  • Basic information

    1. Product Name: 2-(2,3,5,6-tetrafluorophenyl)benzo[d]oxazole
    2. Synonyms: 2-(2,3,5,6-tetrafluorophenyl)benzo[d]oxazole
    3. CAS NO:1567382-95-9
    4. Molecular Formula:
    5. Molecular Weight: 267.182
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1567382-95-9.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: 2-(2,3,5,6-tetrafluorophenyl)benzo[d]oxazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2,3,5,6-tetrafluorophenyl)benzo[d]oxazole(1567382-95-9)
    11. EPA Substance Registry System: 2-(2,3,5,6-tetrafluorophenyl)benzo[d]oxazole(1567382-95-9)

  • 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: 1567382-95-9(Hazardous Substances Data)

1567382-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1567382-95-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,7,3,8 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1567382-95:
(9*1)+(8*5)+(7*6)+(6*7)+(5*3)+(4*8)+(3*2)+(2*9)+(1*5)=209
209 % 10 = 9
So 1567382-95-9 is a valid CAS Registry Number.

1567382-95-9Downstream Products

1567382-95-9Relevant articles and documents

Nickel-catalyzed decarboxylative arylation of heteroarenes through sp2 C-H functionalization

Yang, Ke,Wang, Peng,Zhang, Cheng,Kadi, Adnan A.,Fun, Hoong-Kun,Zhang, Yan,Lu, Hongjian

, p. 7586 - 7589 (2014)

The direct decarboxylative arylation of hetereoarenes with benzoic acids through a nickel-catalyzed sp2 C-H functionalization process was developed. This process provides the first examples of decarboxylative cross-coupling reactions with aroma

Photocatalytic hydrodefluorination: Facile access to partially fluorinated aromatics

Senaweera, Sameera M.,Singh, Anuradha,Weaver, Jimmie D.

, p. 3002 - 3005 (2014/03/21)

Polyfluorinated aromatics are essential to materials science as well as the pharmaceutical and agrochemical industries and yet are often difficult to access. This Communication describes a photocatalytic hydrodefluorination approach which begins with easily accessible perfluoroarenes and selectively reduces the C-F bonds. The method allows facile access to a number of partially fluorinated arenes and takes place with unprecedented catalytic activity using a safe and inexpensive amine as the reductant.

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