2-(fluoromethylsulfonyl)-1,3-benzothiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.
189579-72-4
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Basic information
- Product Name: 2-(fluoromethylsulfonyl)-1,3-benzothiazole
- Synonyms:
- CAS NO:189579-72-4
- Molecular Formula:
- Molecular Weight: 231.272
- EINECS: N/A
- Product Categories: N/A
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Chemical Properties
- Melting Point: 144-147 °C
- Boiling Point: 378.8±44.0 °C(Predicted)
- Flash Point: N/A
- Appearance: N/A
- Density: 1.506±0.06 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 2-(fluoromethylsulfonyl)-1,3-benzothiazole(CAS DataBase Reference)
- NIST Chemistry Reference: 2-(fluoromethylsulfonyl)-1,3-benzothiazole(189579-72-4)
- EPA Substance Registry System: 2-(fluoromethylsulfonyl)-1,3-benzothiazole(189579-72-4)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 189579-72-4(Hazardous Substances Data)
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189579-72-4 Usage
Benzothiazole derivative
A compound based on the benzothiazole structure This indicates that 2-(fluoromethylsulfonyl)-1,3-benzothiazole is derived from the benzothiazole core structure, which is known for its diverse biological activities.Fluoromethylsulfonyl group
A functional group containing a fluorine atom and a sulfonyl group This specific functional group is attached to the benzothiazole core, which may enhance the compound's reactivity and biological properties.Potentially useful building block in organic synthesis
A compound that can be used to create more complex molecules This suggests that 2-(fluoromethylsulfonyl)-1,3-benzothiazole can be utilized as a starting material in the synthesis of more complex organic compounds.Diverse biological activities
A wide range of potential effects on living organisms This highlights the potential for benzothiazole derivatives, including 2-(fluoromethylsulfonyl)-1,3-benzothiazole, to have various biological effects, making them interesting for research.Potential use in pharmaceuticals and agrochemicals
Possible applications in the development of drugs and pesticides This indicates that 2-(fluoromethylsulfonyl)-1,3-benzothiazole and other benzothiazole derivatives could be used in the creation of new pharmaceuticals and agrochemicals due to their diverse biological activities.Enhanced reactivity and biological properties due to fluorine atom
The presence of a fluorine atom may improve the compound's chemical and biological properties This suggests that the fluorine atom in 2-(fluoromethylsulfonyl)-1,3-benzothiazole could make it more reactive and biologically active, increasing its value in medicinal chemistry research and development.Check Digit Verification of cas no
The CAS Registry Mumber 189579-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,5,7 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.Calculate Digit Verification of CAS Registry Number 189579-72:
(8*1)+(7*8)+(6*9)+(5*5)+(4*7)+(3*9)+(2*7)+(1*2)=214
214 % 10 = 4
So 189579-72-4 is a valid CAS Registry Number.
189579-72-4Upstream product
189579-72-4Downstream Products
- 1433994-05-8 C28H29FO4
- 1433994-04-7 2,6-anhydro-4,5,7-tri-O-benzyl-1-deoxy-1-fluoro-D-gluco-hept-1-enitol
- 1433994-07-0 C27H27FO4
- 1433994-06-9 2,5-anhydro-3,4,6-tri-O-benzyl-1-deoxy-1-fluoro-D-arabino-hex-1-enitol
- 1433994-09-2 C12H13FO2
- 1433994-08-1 (R)-3-(benzyloxy)-2-(fluoromethylene)tetrahydrofuran
- 1433994-03-6 2,3,4,6-tetra-O-benzyl-D-gluconolactone
- 1433994-02-5 2,6-anhydro-3,4,5,7-tetra-O-benzyl-1-deoxy-1-fluoro-D-gluco-hept-1-enitol
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2-(fluoromethylsulfonyl)-1,3-benzothiazole
