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1041166-84-0

3-phenyl-6-(trifluoromethyl)-2H-benzo[b][1,4]thiazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1041166-84-0 Structure

  • Basic information

    1. Product Name: 3-phenyl-6-(trifluoromethyl)-2H-benzo[b][1,4]thiazine
    2. Synonyms: 3-phenyl-6-(trifluoromethyl)-2H-benzo[b][1,4]thiazine
    3. CAS NO:1041166-84-0
    4. Molecular Formula:
    5. Molecular Weight: 293.312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1041166-84-0.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: 3-phenyl-6-(trifluoromethyl)-2H-benzo[b][1,4]thiazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-phenyl-6-(trifluoromethyl)-2H-benzo[b][1,4]thiazine(1041166-84-0)
    11. EPA Substance Registry System: 3-phenyl-6-(trifluoromethyl)-2H-benzo[b][1,4]thiazine(1041166-84-0)

  • 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: 1041166-84-0(Hazardous Substances Data)

1041166-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1041166-84-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,1,1,6 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1041166-84:
(9*1)+(8*0)+(7*4)+(6*1)+(5*1)+(4*6)+(3*6)+(2*8)+(1*4)=110
110 % 10 = 0
So 1041166-84-0 is a valid CAS Registry Number.

1041166-84-0Downstream Products

1041166-84-0Relevant articles and documents

Radical Route to 1,4-Benzothiazine Derivatives from 2-Aminobenzenethiols and Ketones under Transition-Metal-Free Conditions

Lin, Ya-mei,Lu, Guo-ping,Wang, Rong-kang,Yi, Wen-bin

supporting information, p. 6424 - 6427 (2016/12/23)

Transition-metal-free radical access to 1,4-benzothiazine derivatives from o-aminobenzenethiols is disclosed. This procedure is available for various ketones including α,β-unsaturated, cyclic, linear, and fluoroalkyl ketones to generate a number of 1,4-benzothiazines, which exist in numerous bioactive and natural molecules, rendering this protocol attractive to both synthetic and medicinal chemistry.

From phenothiazine to 3-phenyl-1,4-benzothiazine derivatives as inhibitors of the Staphylococcus aureus NorA multidrug efflux pump

Sabatini, Stefano,Kaatz, Glenn W.,Rossolini, Gian Maria,Brandini, David,Fravolini, Arnaldo

experimental part, p. 4321 - 4330 (2009/05/07)

Overexpression of efflux pumps is an important mechanism by which bacteria evade effects of substrate antimicrobial agents and inhibition of such pumps is a promising strategy to circumvent this resistance mechanism. NorA is a Staphylococcus aureus multid

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