CAS 155731-14-9 · Sulfur-Containing Compound · 5 functional traits · cGMP compliant · Ships from USA in 2-3 days
5-Chlorothiophene-2-sulfonic acid tert-butylamide (CAS Number: 155731-14-9) is a sulfur-functionalized compound with diverse reactivity featuring a Thiophene ring. ChemContract Research supplies this moderate-complexity compound in high purity from our Huntington Beach, California facility, ensuring consistent quality and reliable domestic delivery throughout the United States.
Sulfonamides are one of the oldest and most successful pharmacophores in medicinal chemistry — present in antibiotics, diuretics, COX-2 inhibitors, and HIV protease inhibitors. Chloro substituents serve a dual role in drug design — as synthetic handles for late-stage functionalization and as bioisosteres that modulate lipophilicity and binding affinity. Heterocyclic rings appear in approximately 85% of all biologically active compounds. The nitrogen, oxygen, or sulfur heteroatom modulates electron density, hydrogen bonding, and aqueous solubility.
Primary applications include sulfonamide pharmacophore installation for antibiotic and diuretic development and nucleophilic aromatic substitution (snar) for ether and amine formation. This compound serves researchers and manufacturers across the pharmaceutical, medicinal chemistry, agrochemical sectors. Whether you require 5-Chlorothiophene-2-sulfonic acid tert-butylamide for early-stage research, process development, or commercial-scale production, ChemContract Research offers flexible ordering from milligram to multi-kilogram quantities with custom synthesis options and full batch documentation including Certificates of Analysis (CoA) and Safety Data Sheets.
How 5-Chlorothiophene-2-sulfonic acid tert-butylamide is used across pharmaceutical and medicinal chemistry sectors
Sulfonamide pharmacophore installation for antibiotic and diuretic development
Nucleophilic aromatic substitution (SNAr) for ether and amine formation
Core scaffold in kinase inhibitor design for oncology therapeutics
Amide bond formation via EDC/HOBt or HATU coupling in peptide synthesis
Peptide bond mimetic for peptidomimetic drug design
Tosyl and mesyl protecting groups for hydroxyl and amine functionalities
Detailed specifications for this sulfur-containing compound, including purity, molecular weight, and analytical data are available upon request. Every batch from ChemContract Research includes:
Some sulfur compounds have strong odors. Handle in a well-ventilated fume hood. Consult the SDS for compound-specific hazards. Some chlorinated compounds are volatile or irritating. Use a fume hood and appropriate PPE. Acid chlorides react vigorously with water. Handle with standard laboratory precautions. Some heterocycles may be hygroscopic or irritating. Use adequate ventilation. Acids may be corrosive or irritating. Handle with chemical-resistant gloves and eye protection. Use a fume hood for volatile acids. Handle with standard laboratory precautions. Consult the SDS for compound-specific hazards.
Store in a cool, dry place in a tightly sealed container. Protect from moisture and light as specified. Store at recommended temperature in a well-sealed container. Protect from moisture and strong bases. Store at recommended temperature in a tightly sealed container. Some heterocyclic compounds are light-sensitive. Store at room temperature in a tightly sealed container. Protect from moisture and strong bases. Store at room temperature or as specified. Keep tightly sealed and protect from moisture.
Every batch of 5-Chlorothiophene-2-sulfonic acid tert-butylamide is produced under cGMP conditions with full CoA documentation, HPLC purity verification, and lot traceability.
Ship from our Huntington Beach, CA facility with 2-3 business day domestic delivery. No import delays, no customs fees, no tariff surprises.
Need a specific grade, quantity, or derivative of 5-Chlorothiophene-2-sulfonic acid tert-butylamide? Our team of PhD chemists can develop custom synthesis solutions for your exact requirements.
Common questions about 5-Chlorothiophene-2-sulfonic acid tert-butylamide
5-Chlorothiophene-2-sulfonic acid tert-butylamide is a sulfur-functionalized compound with diverse reactivity used primarily in the pharmaceutical and medicinal chemistry industries. Key applications include sulfonamide pharmacophore installation for antibiotic and diuretic development and nucleophilic aromatic substitution (snar) for ether and amine formation.
ChemContract Research is a trusted USA-based supplier of 5-Chlorothiophene-2-sulfonic acid tert-butylamide. We offer competitive pricing, fast domestic shipping from our Huntington Beach, California facility, and full quality documentation including Certificates of Analysis (CoA). Request a quote at chemistry@chem-contract.com or call +1 (714) 732-8549.
ChemContract Research supplies 5-Chlorothiophene-2-sulfonic acid tert-butylamide in multiple purity grades: ≥95% standard grade, ≥97% high-purity grade, and ≥99% ultra-high-purity grade depending on application requirements. We can also provide custom purity grades through our synthesis capabilities. Contact us for specific purity information and CoA documentation.
Yes. ChemContract Research offers custom synthesis services for 5-Chlorothiophene-2-sulfonic acid tert-butylamide from milligram to multi-kilogram scale. Our cGMP-compliant facilities and experienced chemists can accommodate custom specifications, packaging requirements, and delivery timelines. Contact our team to discuss your project.
For amide bond formation from the carboxylic acid in 5-Chlorothiophene-2-sulfonic acid tert-butylamide, HATU/DIPEA is recommended for peptide coupling (high yield, low epimerization). EDC/HOBt is a cost-effective alternative for non-peptide amides. T3P (propylphosphonic acid anhydride) offers excellent atom economy with easy workup. For ester formation, DCC/DMAP (Steglich conditions) or Mitsunobu conditions are standard.
As a chlorinated compound, 5-Chlorothiophene-2-sulfonic acid tert-butylamide is an excellent substrate for palladium-catalyzed cross-coupling reactions including Suzuki, Heck, Negishi, Sonogashira, and Buchwald–Hartwig amination. It can also be used for Grignard reagent preparation, metal–halogen exchange with organolithium reagents, and nucleophilic substitution reactions.
Store in a cool, dry place in a tightly sealed container. Protect from moisture and light as specified. Store at recommended temperature in a well-sealed container. Protect from moisture and strong bases. Store at recommended temperature in a tightly sealed container. Some heterocyclic compounds are light-sensitive. Store at room temperature in a tightly sealed container. Protect from moisture and strong bases. Store at room temperature or as specified. Keep tightly sealed and protect from moisture. Always consult the compound-specific Safety Data Sheet (SDS) provided with your order for detailed storage requirements. ChemContract Research includes handling and storage documentation with every shipment.
The CAS Registry Number for 5-Chlorothiophene-2-sulfonic acid tert-butylamide is 155731-14-9. This unique identifier is used worldwide to reference this specific compound in chemical databases, regulatory filings, and scientific literature. ChemContract Research supplies this compound with full quality documentation. Contact us at chemistry@chem-contract.com for availability and pricing.
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