(6-nitro-benzothiazol-2-ylsulfanyl)-acetic acid is a chemical compound characterized by its molecular formula C9H6N2O4S. It is a derivative of sulfanyl-acetic acid, featuring a benzothiazole ring with a nitro group at the 6-position. (6-nitro-benzothiazol-2-ylsulfanyl)-acetic acid holds promise as a reagent in chemical synthesis and serves as a building block for the creation of various organic compounds. Additionally, it may possess biological activity, but further research is required to ascertain its full potential in this regard.
1653-46-9
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Basic information
- Product Name: (6-nitro-benzothiazol-2-ylsulfanyl)-acetic acid
- Synonyms:
- CAS NO:1653-46-9
- Molecular Formula:
- Molecular Weight: 270.29
- EINECS: N/A
- Product Categories: N/A
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: (6-nitro-benzothiazol-2-ylsulfanyl)-acetic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (6-nitro-benzothiazol-2-ylsulfanyl)-acetic acid(1653-46-9)
- EPA Substance Registry System: (6-nitro-benzothiazol-2-ylsulfanyl)-acetic acid(1653-46-9)
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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: 1653-46-9(Hazardous Substances Data)
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1653-46-9 Usage
Uses
Used in Chemical Synthesis:(6-nitro-benzothiazol-2-ylsulfanyl)-acetic acid is used as a reagent in chemical synthesis for its ability to contribute to the formation of complex organic molecules. Its unique structure, including the benzothiazole ring and nitro group, allows it to participate in a range of chemical reactions, facilitating the synthesis of diverse compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (6-nitro-benzothiazol-2-ylsulfanyl)-acetic acid is used as a building block for the preparation of various organic compounds with potential medicinal properties. Its incorporation into drug candidates may lead to the development of new therapeutic agents, particularly if its biological activity is confirmed through further research.
Used in Material Science:
(6-nitro-benzothiazol-2-ylsulfanyl)-acetic acid may also find applications in material science, where its unique chemical structure could be leveraged to create novel materials with specific properties. These materials could have uses in various industries, such as electronics, where they might be employed in the development of advanced sensors or other components.
Check Digit Verification of cas no
The CAS Registry Mumber 1653-46-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,5 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.Calculate Digit Verification of CAS Registry Number 1653-46:
(6*1)+(5*6)+(4*5)+(3*3)+(2*4)+(1*6)=79
79 % 10 = 9
So 1653-46-9 is a valid CAS Registry Number.
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(6-nitro-benzothiazol-2-ylsulfanyl)-acetic acid
