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· · COA & SDS available for every product · Same-day shipping on in-stock items (S)-(-)-3-(Boc-amino)pyrrolidine - ≥98% , CAS No.122536-76-9
Synonyms
tert-Butyl 3-pyrrolidinylcarbamate | 3-(s)-tert-butoxycarbonylaminopyrrolidine | (S)-3-(Boc-amino)pyrrolidine, >=98.0% (TLC) | HY-79691 | (S)-3-(tert.-butyloxycarbonylamino)pyrrolidine | tert-butyl (3S)-pyrrolidin-3-ylcarbamate | (S)-3-(Boc-amino)pyrrolid
Storage
Argon charged,Room temperature
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview Application：
(S)-3-(Boc-amino)pyrrolidine can be used as a building block to prepare:
2,4,6-trisubstitued pyrido[3,4-d]pyrimidine derivatives as potent inhibitors against EGFR tyrosine kinase.
Aminopyrrolidine scaffolds for asymmetric Morita−Baylis-Hillman reaction.
N-benzyl-3-sulfonamidopyrrolidines as potent bacterial cell division inhibitors.
Specifications Synonyms
tert-Butyl 3-pyrrolidinylcarbamate | 3-(s)-tert-butoxycarbonylaminopyrrolidine | (S)-3-(Boc-amino)pyrrolidine, >=98.0% (TLC) | HY-79691 | (S)-3-(tert.-butyloxycarbonylamino)pyrrolidine | tert-butyl (3S)-pyrrolidin-3-ylcarbamate | (S)-3-(Boc-amino)pyrrolid
Specifications & Purity
≥98%
Storage
Argon charged, Room temperature
Names and Identifiers Pubchem Sid 488191905 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488191905 Canonical Smiles CC(C)(C)OC(=O)NC1CCNC1 IUPAC Name tert-butyl N-[(3S)-pyrrolidin-3-yl]carbamate InChIKey DQQJBEAXSOOCPG-ZETCQYMHSA-N INCHI 1S/C9H18N2O2/c1-9(2,3)13-8(12)11-7-4-5-10-6-7/h7,10H,4-6H2,1-3H3,(H,11,12)/t7-/m0/s1 Isomeric SMILES CC(C)(C)OC(=O)N[C@H]1CCNC1 WGK Germany 3 Molecular Weight 186.25 Beilstein 5377810 Reaxy-Rn 4180161 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4180161&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organoheterocyclic compounds Class Pyrrolidines Subclass Not available Intermediate Tree Nodes Not available Direct Parent Pyrrolidines Alternative Parents Carbamate esters Organic carbonic acids and derivatives Dialkylamines Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic heteromonocyclic compounds Substituents Pyrrolidine - Carbamic acid ester - Carbonic acid derivative - Secondary aliphatic amine - Secondary amine - Azacycle - Organopnictogen compound - Amine - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Aliphatic heteromonocyclic compound Description This compound belongs to the class of organic compounds known as pyrrolidines. These are compounds containing a pyrrolidine ring, which is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Chloroform (Slightly), Methanol (Slightly) Sensitivity air sensitive Specific Rotation[α] -20° (C=1,EtOH) Melt Point(°C) 50-54°C Molecular Weight 186.250 g/mol XLogP3 0.700 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 3 Exact Mass 186.137 Da Monoisotopic Mass 186.137 Da Topological Polar Surface Area 50.400 Ų Heavy Atom Count 13 Formal Charge 0 Complexity 187.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 1 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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