Cas no 883555-11-1 (Carbamicacid, N-[5-(ethylamino)pentyl]-, 1,1-dimethylethyl ester)

Carbamic acid, N-[5-(ethylamino)pentyl]-, 1,1-dimethylethyl ester is a specialized carbamate ester compound featuring a tertiary butyl (t-Boc) protecting group and an ethylamino pentyl side chain. This structural configuration enhances its utility in organic synthesis, particularly in peptide coupling and amine protection strategies. The t-Boc group offers selective deprotection under mild acidic conditions, ensuring compatibility with sensitive substrates. The ethylamino pentyl moiety provides flexibility for further functionalization, making it valuable in medicinal chemistry and drug development. Its stability under basic conditions and controlled reactivity make it a preferred intermediate for constructing complex molecular architectures. Suitable for research applications requiring precise amine protection and controlled release.
Carbamicacid, N-[5-(ethylamino)pentyl]-, 1,1-dimethylethyl ester structure
883555-11-1 structure
Product Name:Carbamicacid, N-[5-(ethylamino)pentyl]-, 1,1-dimethylethyl ester
CAS No:883555-11-1
MF:C12H26N2O2
MW:230.347043514252
CID:721168
PubChem ID:26369702
Update Time:2025-10-05

Carbamicacid, N-[5-(ethylamino)pentyl]-, 1,1-dimethylethyl ester Chemical and Physical Properties

Names and Identifiers

    • Carbamicacid, N-[5-(ethylamino)pentyl]-, 1,1-dimethylethyl ester
    • tert-Butyl 5-(ethylamino)pentylcarbamate
    • tert-butyl N-[5-(ethylamino)pentyl]carbamate
    • AmbotzBNN1041
    • N'-Ethylpentane-1,5-diamine, N-BOC protected 95%
    • tert-Butyl [5-(ethylamino)pentyl]carbamate, 1-[(tert-Butoxycarbonyl)amino]-5-(ethylamino)pentane
    • Carbamic acid, N-[5-(ethylamino)pentyl]-, 1,1-dimethylethyl ester
    • MS-21782
    • DTXSID00649973
    • AKOS030212281
    • tert-Butyl (5-(ethylamino)pentyl)carbamate
    • A1-18828
    • 883555-11-1
    • DB-077267
    • tert-Butyl [5-(ethylamino)pentyl]carbamate
    • Carbamicacid,N-[5-(ethylamino)pentyl]-,1,1-dimethylethyl ester
    • Inchi: 1S/C12H26N2O2/c1-5-13-9-7-6-8-10-14-11(15)16-12(2,3)4/h13H,5-10H2,1-4H3,(H,14,15)
    • InChI Key: HSYFFBMGEABTLW-UHFFFAOYSA-N
    • SMILES: C(OC(C)(C)C)(=O)NCCCCCNCC

Computed Properties

  • Exact Mass: 230.19900
  • Monoisotopic Mass: 230.199428076g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 9
  • Complexity: 188
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.9
  • Topological Polar Surface Area: 50.4?2

Experimental Properties

  • PSA: 50.36000
  • LogP: 3.07270

Carbamicacid, N-[5-(ethylamino)pentyl]-, 1,1-dimethylethyl ester Security Information

  • Hazard Statement: Irritant
  • Hazardous Material Identification: Xi

Carbamicacid, N-[5-(ethylamino)pentyl]-, 1,1-dimethylethyl ester Customs Data

  • HS CODE:2921490090

Carbamicacid, N-[5-(ethylamino)pentyl]-, 1,1-dimethylethyl ester Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Key Organics Ltd
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Additional information on Carbamicacid, N-[5-(ethylamino)pentyl]-, 1,1-dimethylethyl ester

Comprehensive Overview of Carbamicacid, N-[5-(ethylamino)pentyl]-, 1,1-dimethylethyl ester (CAS No. 883555-11-1)

The compound Carbamicacid, N-[5-(ethylamino)pentyl]-, 1,1-dimethylethyl ester (CAS No. 883555-11-1) is a specialized organic molecule with significant applications in pharmaceutical and chemical research. This ester derivative of carbamic acid features a unique structure, combining an ethylamino pentyl chain with a tert-butyl ester group. Its molecular formula and weight make it a subject of interest for researchers exploring novel bioactive compounds and synthetic intermediates.

In recent years, the demand for Carbamicacid derivatives has surged due to their versatility in drug discovery and material science. The 1,1-dimethylethyl ester moiety, in particular, is valued for its stability and reactivity, making it a key functional group in protecting strategies during multi-step organic syntheses. Researchers frequently search for "CAS 883555-11-1 applications" or "N-[5-(ethylamino)pentyl] carbamate synthesis," reflecting its growing relevance in academic and industrial settings.

The compound's structural attributes align with current trends in green chemistry and sustainable synthesis. Its potential as a building block for biodegradable polymers or enzyme inhibitors has sparked discussions in forums focusing on eco-friendly chemical alternatives. Analytical techniques like HPLC and NMR are commonly employed to characterize Carbamicacid, N-[5-(ethylamino)pentyl] derivatives, as evidenced by frequent queries about "883555-11-1 spectral data" in scientific databases.

From a commercial perspective, suppliers often highlight the high purity grade of CAS No. 883555-11-1 to meet stringent laboratory requirements. The compound's shelf life and storage conditions (typically 2-8°C under inert atmosphere) are critical considerations for buyers, as indicated by search terms like "tert-butyl carbamate storage guidelines." Regulatory compliance with REACH and other global standards further enhances its marketability.

Emerging studies suggest potential applications of this carbamic acid ester in peptide mimetics and drug delivery systems, correlating with increased interest in "targeted molecular carriers" across biomedical literature. The ethylamino pentyl chain's amphiphilic properties may contribute to enhanced cellular permeability—a hot topic in bioavailability optimization research.

Quality control protocols for CAS 883555-11-1 typically involve rigorous testing for residual solvents and heavy metals, addressing the pharmaceutical industry's focus on "impurity profiling." This aligns with current Good Manufacturing Practice (cGMP) requirements, making the compound suitable for preclinical development stages.

Future research directions may explore the compound's utility in catalysis or as a precursor for functionalized nanomaterials, areas generating substantial interest in materials science communities. The tert-butoxycarbonyl (Boc) protecting group's cleavage characteristics remain a subject of investigation, particularly for "acid-labile protecting groups" in combinatorial chemistry.

In summary, Carbamicacid, N-[5-(ethylamino)pentyl]-, 1,1-dimethylethyl ester represents a multifaceted compound bridging synthetic chemistry and applied research. Its evolving applications continue to inspire both commercial inquiries ("bulk suppliers of 883555-11-1") and academic investigations into molecular design principles, ensuring its sustained relevance across scientific disciplines.

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