CAS 914349-53-4 · Piperazine · 3 functional traits · cGMP compliant · Ships from USA in 2-3 days
2-(4-N-Boc-Piperazin-1-yl)methylbenzoic acid (CAS Number: 914349-53-4) is a piperazine-containing compound used extensively as a pharmacokinetic-enhancing motif featuring a Piperazine 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.
The two nitrogen atoms of piperazine provide both a basic amine (pKa ~9.8) for salt formation and a secondary amine (pKa ~5.3) for functionalization, giving medicinal chemists dual synthetic handles. The Boc group is removed cleanly with TFA or HCl in dioxane, making it orthogonal to Fmoc, Cbz, and Alloc protecting groups — essential for synthesizing complex peptide therapeutics. Carboxylic acids are among the most synthetically versatile functional groups — they can be converted to amides, esters, acid chlorides, anhydrides, alcohols, and aldehydes in a single step.
Primary applications include solubility enhancer via piperazine salt formation in drug formulation and solid-phase peptide synthesis (spps) with orthogonal boc/fmoc strategies. This compound serves researchers and manufacturers across the pharmaceutical, cns therapeutics, medicinal chemistry sectors. Whether you require 2-(4-N-Boc-Piperazin-1-yl)methylbenzoic acid 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 2-(4-N-Boc-Piperazin-1-yl)methylbenzoic acid is used across pharmaceutical and cns therapeutics sectors
Solubility enhancer via piperazine salt formation in drug formulation
Solid-phase peptide synthesis (SPPS) with orthogonal Boc/Fmoc strategies
Amide bond formation via EDC/HOBt or HATU coupling in peptide synthesis
Bioisosteric replacement for piperidine to improve metabolic profile
Multi-step pharmaceutical synthesis requiring selective amine deprotection
Salt formation with amines to improve drug crystallinity and stability
Detailed specifications for this piperazine, including purity, molecular weight, and analytical data are available upon request. Every batch from ChemContract Research includes:
Handle with standard precautions. Some piperazine derivatives may be irritating. Use adequate ventilation. Boc-protected compounds are generally stable. TFA deprotection generates isobutylene gas — perform in a fume hood. Acids may be corrosive or irritating. Handle with chemical-resistant gloves and eye protection. Use a fume hood for volatile acids.
Store at room temperature in a tightly sealed container away from acids. Store at room temperature in a sealed container. Stable under neutral and basic conditions; avoid strong acids during storage. Store at room temperature in a tightly sealed container. Protect from moisture and strong bases.
Piperazine motifs improve drug solubility. 2-(4-N-Boc-Piperazin-1-yl)methylbenzoic acid is available with salt-form screening data to accelerate your formulation development.
Every batch of 2-(4-N-Boc-Piperazin-1-yl)methylbenzoic acid 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 2-(4-N-Boc-Piperazin-1-yl)methylbenzoic acid? Our team of PhD chemists can develop custom synthesis solutions for your exact requirements.
Common questions about 2-(4-N-Boc-Piperazin-1-yl)methylbenzoic acid
2-(4-N-Boc-Piperazin-1-yl)methylbenzoic acid is a piperazine-containing compound used extensively as a pharmacokinetic-enhancing motif used primarily in the pharmaceutical and cns therapeutics industries. Key applications include solubility enhancer via piperazine salt formation in drug formulation and solid-phase peptide synthesis (spps) with orthogonal boc/fmoc strategies.
ChemContract Research is a trusted USA-based supplier of 2-(4-N-Boc-Piperazin-1-yl)methylbenzoic acid. 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 2-(4-N-Boc-Piperazin-1-yl)methylbenzoic acid 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 2-(4-N-Boc-Piperazin-1-yl)methylbenzoic acid 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 2-(4-N-Boc-Piperazin-1-yl)methylbenzoic acid, 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.
The Boc protecting group in 2-(4-N-Boc-Piperazin-1-yl)methylbenzoic acid is cleanly removed by treatment with trifluoroacetic acid (TFA, 20–50% in DCM) at room temperature, typically within 30–60 minutes. Alternative conditions include HCl in dioxane (4M) or trimethylsilyl triflate with 2,6-lutidine. The Boc group is stable to base, hydrogenation, and many nucleophilic conditions, making it orthogonal to Fmoc and Cbz groups.
Store at room temperature in a tightly sealed container away from acids. Store at room temperature in a sealed container. Stable under neutral and basic conditions; avoid strong acids during storage. Store at room temperature in a tightly sealed container. Protect from moisture and strong bases. 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 2-(4-N-Boc-Piperazin-1-yl)methylbenzoic acid is 914349-53-4. 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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