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2-(phenylsulfonyl)-3-(trifluoromethyl)oxirane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 533887-24-0 Structure
  • Basic information

    1. Product Name: 2-(phenylsulfonyl)-3-(trifluoromethyl)oxirane
    2. Synonyms: 2-(phenylsulfonyl)-3-(trifluoromethyl)oxirane
    3. CAS NO:533887-24-0
    4. Molecular Formula:
    5. Molecular Weight: 252.214
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 533887-24-0.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: 2-(phenylsulfonyl)-3-(trifluoromethyl)oxirane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(phenylsulfonyl)-3-(trifluoromethyl)oxirane(533887-24-0)
    11. EPA Substance Registry System: 2-(phenylsulfonyl)-3-(trifluoromethyl)oxirane(533887-24-0)
  • 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: 533887-24-0(Hazardous Substances Data)

533887-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 533887-24-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,3,8,8 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 533887-24:
(8*5)+(7*3)+(6*3)+(5*8)+(4*8)+(3*7)+(2*2)+(1*4)=180
180 % 10 = 0
So 533887-24-0 is a valid CAS Registry Number.

533887-24-0Relevant articles and documents

Thiazolides as novel antiviral agents. 1. Inhibition of hepatitis B virus replication

Stachulski, Andrew V.,Pidathala, Chandrakala,Row, Eleanor C.,Sharma, Raman,Berry, Neil G.,Iqbal, Mazhar,Bentley, Joanne,Allman, Sarah A.,Edwards, Geoffrey,Helm, Alison,Hellier, Jennifer,Korba, Brent E.,Semple, J. Edward,Rossignol, Jean-Francois

supporting information; experimental part, p. 4119 - 4132 (2011/08/05)

We report the syntheses and activities of a wide range of thiazolides [viz., 2-hydroxyaroyl-N-(thiazol-2-yl)amides] against hepatitis B virus replication, with QSAR analysis of our results. The prototypical thiazolide, nitazoxanide [2-hydroxybenzoyl-N-(5-

CARBACEPHEM β-LACTAM ANTIBIOTICS

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Page/Page column 92, (2010/04/06)

Carbacephem -lactam antibiotics having structure (I) are disclosed, including stereoisomers, pharmaceutically acceptable salts, esters and prodrugs thereof, wherein Ar1, Ar2, R1 and R2 are as defined herein. The compounds are useful for the treatment of bacterial infections, in particular those caused by methicillin-resistant Staphylococcus spp.

CARBACEPHEM BETA-LACTAM ANTIBIOTICS

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Page/Page column 65; 88, (2010/11/05)

Carbacephem β-lactam antibiotics having chemical structures (I) and (II) are disclosed: including stereoisomers, pharmaceutically acceptable salts, esters and prodrugs thereof, wherein Ar2, R1, R2 and R6 are as defined herein. The compounds are useful for the treatment of bacterial infections, in particular those caused by methicillin-resistant Staphylococcus spp.

HALOALKYL HETEROARYL BENZAMIDE COMPOUNDS

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Page/Page column 129-130, (2010/12/17)

A new class of haloalkyl heteroaryl benzamides is described. These compounds show strong activity against hepatitis viruses.

[4-(HETEROARYL) PIPERAZIN-1-YL]-(2,5-SUBSTITUTED -PHENYL)METHANONE DERIVATIVES AS GLYCINE TRANSPORTER 1 (GLYT-1) INHIBITORS FOR THE TREATMENT OF NEUROLOGICAL AND NEUROPSYCHIATRIC DISORDERS

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Page/Page column 65, (2008/06/13)

The present invention relates to compounds of the general formula (I) wherein R1 is-OR1’,-SR1’ or is a heterocycloalkyl group; R1’ is lower alkyl, lower alkyl substituted by halogen or is -(CH2)n

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