68959-22-8
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Basic information
- Product Name: 1,2-dimethyl-3-[(4-sulphonatophenyl)methyl]-5-(trifluoromethyl)-1H-benzimidazolium
- Synonyms: 1,2-dimethyl-3-[(4-sulphonatophenyl)methyl]-5-(trifluoromethyl)-1H-benzimidazolium;1,2-Dimethyl-3-[(4-sulfonatophenyl)methyl]-5-(trifluoromethyl)-1H-benzimidazol-3-ium
- CAS NO:68959-22-8
- Molecular Formula: C17H15F3N2O3S
- Molecular Weight: 384.3728096
- EINECS: 273-406-0
- Product Categories: N/A
- Mol File: 68959-22-8.mol
- Article Data: 0
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 1,2-dimethyl-3-[(4-sulphonatophenyl)methyl]-5-(trifluoromethyl)-1H-benzimidazolium(CAS DataBase Reference)
- NIST Chemistry Reference: 1,2-dimethyl-3-[(4-sulphonatophenyl)methyl]-5-(trifluoromethyl)-1H-benzimidazolium(68959-22-8)
- EPA Substance Registry System: 1,2-dimethyl-3-[(4-sulphonatophenyl)methyl]-5-(trifluoromethyl)-1H-benzimidazolium(68959-22-8)
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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: 68959-22-8(Hazardous Substances Data)
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Chemical structure
A complex structure consisting of a benzimidazole ring with a methyl and trifluoromethyl group attached, and a sulphonatophenyl group.Methyl group
A single carbon atom bonded to three hydrogen atoms.Trifluoromethyl group
A carbon atom bonded to three fluorine atoms.Sulphonatophenyl group
A phenyl ring with a sulphonate group attached.Organic synthesis
Used in the creation of various organic compounds.Catalyst
Facilitates chemical reactions, increasing their rate and efficiency.Binding ability
The sulphonatophenyl group can bind to other molecules, allowing for various chemical reactions to occur.Unique properties
The combination of functional groups and the benzimidazole ring structure gives this compound its unique properties, making it useful in various applications in the field of chemistry and chemical engineering.Charge
The compound has a positive charge due to the presence of the benzimidazolium cation.Solubility
Depending on the specific conditions, this compound may be soluble in polar solvents such as water or dimethyl sulfoxide (DMSO) due to the presence of the sulphonatophenyl group.Stability
The compound is likely to be stable under normal conditions, but may be sensitive to extreme temperatures, pH levels, or the presence of certain chemicals.Reactivity
The compound may be reactive with nucleophiles, electrophiles, or other reactive species, depending on the specific reaction conditions and the presence of other reactants.Synthesis
The compound can be synthesized through various chemical reactions, likely involving the formation of the benzimidazole ring, attachment of the functional groups, and subsequent modifications.Check Digit Verification of cas no
The CAS Registry Mumber 68959-22-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,9,5 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.Calculate Digit Verification of CAS Registry Number 68959-22:
(7*6)+(6*8)+(5*9)+(4*5)+(3*9)+(2*2)+(1*2)=188
188 % 10 = 8
So 68959-22-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H15F3N2O3S/c1-11-21(2)15-8-5-13(17(18,19)20)9-16(15)22(11)10-12-3-6-14(7-4-12)26(23,24)25/h3-9H,10H2,1-2H3
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1,2-dimethyl-3-[(4-sulphonatophenyl)methyl]-5-(trifluoromethyl)-1H-benzimidazolium
