1-(triisopropylsilyl)-1H-indole-6-sulfonyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.
912846-33-4
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Basic information
- Product Name: 1-(triisopropylsilyl)-1H-indole-6-sulfonyl chloride
- Synonyms: 1-(triisopropylsilyl)-1H-indole-6-sulfonyl chloride
- CAS NO:912846-33-4
- Molecular Formula:
- Molecular Weight: 372.003
- 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: 1-(triisopropylsilyl)-1H-indole-6-sulfonyl chloride(CAS DataBase Reference)
- NIST Chemistry Reference: 1-(triisopropylsilyl)-1H-indole-6-sulfonyl chloride(912846-33-4)
- EPA Substance Registry System: 1-(triisopropylsilyl)-1H-indole-6-sulfonyl chloride(912846-33-4)
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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: 912846-33-4(Hazardous Substances Data)
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912846-33-4 Usage
Chemical structure
A sulfonyl chloride derivative of indole with a triisopropylsilyl group attached to the nitrogen atom.Indole
A heterocyclic compound commonly found in natural products and pharmaceuticals.Sulfonyl chloride
A versatile functional group used for synthetic transformations.Triisopropylsilyl
A protecting group used to block reactive sites in organic synthesis.Organic synthesis
As a building block for the synthesis of biologically active compounds.Pharmaceutical research
For the development of potential pharmaceutical applications.Nucleophilic substitution reactions
The sulfonyl chloride group can react with nucleophiles to form new compounds.Cross-coupling reactions
The sulfonyl chloride group can participate in cross-coupling reactions to form carbon-sulfur bonds.Protecting group
The triisopropylsilyl group serves as a temporary protecting group, allowing for selective reactions to occur at other sites in the molecule.Reactivity
The sulfonyl chloride group is highly reactive towards nucleophiles, making it a useful intermediate for various synthetic pathways.Stability
The triisopropylsilyl group provides stability to the molecule, protecting the indole core from unwanted side reactions.Solubility
The compound is likely to be soluble in common organic solvents, such as dichloromethane, tetrahydrofuran, or dimethyl sulfoxide, due to its nonpolar nature.Purity
The compound should be stored and handled under anhydrous conditions to prevent hydrolysis of the sulfonyl chloride group.Safety precautions
As with any chemical compound, appropriate safety measures should be taken when handling 1-(triisopropylsilyl)-1H-indole-6-sulfonyl chloride, including the use of gloves, eye protection, and a well-ventilated workspace.Check Digit Verification of cas no
The CAS Registry Mumber 912846-33-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,2,8,4 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.Calculate Digit Verification of CAS Registry Number 912846-33:
(8*9)+(7*1)+(6*2)+(5*8)+(4*4)+(3*6)+(2*3)+(1*3)=174
174 % 10 = 4
So 912846-33-4 is a valid CAS Registry Number.
912846-33-4Upstream product
912846-33-4Downstream Products
- 1423161-83-4 N-(2,4-dimethoxybenzyl)-3-(2-(1-methyl-1H-pyrazol-5-yl)-4-(trifluoromethyl)phenyl)-N-(1,2,4-thiadiazol-5-yl)-1H-indole-6-sulfonamide
- 1423161-82-3 3-bromo-N-(2,4-dimethoxybenzyl)-N-(1,2,4-thiadiazol-5-yl)-1H-indole-6-sulfonamide
- 1423160-82-0 C23H17F3N6O3S2
- 1423160-80-8 C24H21F3N6O2S2
- 1423160-78-4 3-(4-chloro-2-(1-methyl-1H-pyrazol-5-yl)phenyl)-1-methyl-N-(1,2,4-thiadiazol-5-yl)-1H-indole-6-sulfonamide
- 1423161-72-1 C20H15ClN6O2S2
- 1423161-71-0 3-(4-chloro-2-(1-methyl-1H-pyrazol-5-yl)phenyl)-N-(2,4-dimethoxybenzyl)-N-(1,2,4-thiadiazol-5-yl)-1H-indole-6-sulfonamide
- 1293979-55-1 C22H23FN4O3S
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1-(triisopropylsilyl)-1H-indole-6-sulfonyl chloride
