Cas no 173606-50-3 (10-(N-Boc-amino)decanoic Acid)

10-(N-Boc-amino)decanoic Acid is a protected amino acid derivative featuring a Boc (tert-butoxycarbonyl) group and a decanoic acid backbone. This compound is widely utilized in peptide synthesis, where the Boc group serves as a temporary protecting group for the amine functionality, enabling selective deprotection under mild acidic conditions. The extended hydrocarbon chain enhances solubility in organic solvents, facilitating coupling reactions in solid-phase and solution-phase peptide chemistry. Its structural versatility makes it valuable for constructing spacer arms in bioconjugation and linker design for drug delivery systems. The product is characterized by high purity and stability, ensuring reliable performance in synthetic applications.
10-(N-Boc-amino)decanoic Acid structure
10-(N-Boc-amino)decanoic Acid structure
Product Name:10-(N-Boc-amino)decanoic Acid
CAS No:173606-50-3
MF:C15H29NO4
MW:287.395065069199
MDL:MFCD00270351
CID:905899
PubChem ID:4321832
Update Time:2025-05-20

10-(N-Boc-amino)decanoic Acid Chemical and Physical Properties

Names and Identifiers

    • 10-((tert-Butoxycarbonyl)amino)decanoic acid
    • BOC-10-AMINODECANOIC ACID
    • 10-(N-Boc-amino)decanoic Acid
    • 10-[(2-methylpropan-2-yl)oxycarbonylamino]decanoic acid
    • BOC-10-ADC-OH
    • 10-(Boc-amino)decanoic acid
    • N-tert-Butoxycarbonylamino-10-decanoic acid
    • N-T-BUTYLOXYCARBONYL-10-AMINO-DECANOIC ACID
    • N-TERT-BUTYLOXYCARBONYL-10-AMINO-DECANOIC ACID
    • 10-[[(1,1-DiMethylethoxy)carbonyl]aMino]decanoic Acid
    • MFCD00270351
    • AKOS007930090
    • 173606-50-3
    • Decanoic acid, 10-[[(1,1-dimethylethoxy)carbonyl]amino]-
    • AB92445
    • 10-{[(tert-butoxy)carbonyl]amino}decanoic acid
    • BP-28241
    • SY199182
    • 10-[(TERT-BUTOXYCARBONYL)AMINO]DECANOIC ACID
    • SCHEMBL2702010
    • DB-311684
    • CS-0131704
    • AS-70153
    • EN300-201194
    • DTXSID00401912
    • Z1505703853
    • D95455
    • Boc-10-aminodecanoic acid≥ 99% (HPLC)
    • MDL: MFCD00270351
    • Inchi: 1S/C15H29NO4/c1-15(2,3)20-14(19)16-12-10-8-6-4-5-7-9-11-13(17)18/h4-12H2,1-3H3,(H,16,19)(H,17,18)
    • InChI Key: DUNPXMOBBKBKHK-UHFFFAOYSA-N
    • SMILES: O(C(NCCCCCCCCCC(=O)O)=O)C(C)(C)C

Computed Properties

  • Exact Mass: 287.21000
  • Monoisotopic Mass: 287.20965841 g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 20
  • Rotatable Bond Count: 13
  • Complexity: 284
  • 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
  • Molecular Weight: 287.39
  • XLogP3: 3.7
  • Topological Polar Surface Area: 75.6?2

Experimental Properties

  • PSA: 75.63000
  • LogP: 4.10740

10-(N-Boc-amino)decanoic Acid Customs Data

  • HS CODE:2924199090
  • Customs Data:

    China Customs Code:

    2924199090

    Overview:

    2924199090. Other acyclic amides(Including acyclic carbamates)(Including its derivatives and salts). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to, packing

    Summary:

    2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

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10-(N-Boc-amino)decanoic Acid Production Method

Additional information on 10-(N-Boc-amino)decanoic Acid

10-(N-Boc-amino)decanoic Acid: A Comprehensive Overview

10-(N-Boc-amino)decanoic acid, also known by its CAS number 173606-50-3, is a compound of significant interest in the fields of organic chemistry, biochemistry, and material science. This compound is a derivative of decanoic acid, with a specific modification at the 10th carbon position. The presence of the Boc (tert-butoxycarbonyl) protecting group on the amino functional group introduces unique chemical properties that make it valuable for various applications.

The structure of 10-(N-Boc-amino)decanoic acid consists of a decanoic acid backbone with a Boc-protected amino group at the terminal position. This structure allows for versatile reactivity, particularly in peptide synthesis and other amine-based reactions. The Boc group serves as a temporary protective group, which can be easily removed under specific conditions to reveal the free amine functionality. This feature makes the compound highly useful in organic synthesis, where precise control over functional groups is essential.

Recent advancements in chemical synthesis have highlighted the potential of 10-(N-Boc-amino)decanoic acid in the development of novel biomaterials. Researchers have explored its use in creating self-assembling peptides, which are critical for tissue engineering and drug delivery systems. The ability to manipulate the Boc group enables fine-tuning of the compound's properties, such as hydrophobicity and reactivity, making it suitable for diverse applications.

In addition to its role in material science, 10-(N-Boc-amino)decanoic acid has gained attention in pharmacology. Studies have demonstrated its potential as a precursor for bioactive molecules, including antibiotics and anticancer agents. The compound's unique structure allows for the incorporation of various functional groups, enhancing its versatility in drug design.

The synthesis of 10-(N-Boc-amino)decanoic acid typically involves multi-step reactions, including alkylation and protection/deprotection strategies. Recent research has focused on optimizing these processes to improve yield and purity. For instance, microwave-assisted synthesis has been employed to accelerate reaction times while maintaining high selectivity.

The application of 10-(N-Boc-amino)decanoic acid extends to analytical chemistry as well. Its use as a calibration standard in mass spectrometry has been reported, highlighting its importance in accurate quantification of related compounds. Furthermore, its role in peptide mapping and structural elucidation has been explored, underscoring its utility in proteomics research.

In conclusion, 10-(N-Boc-amino)decanoic acid, with its CAS number 173606-50-3, stands as a versatile compound with wide-ranging applications across multiple disciplines. Its unique chemical properties and modular structure make it an invaluable tool in organic synthesis, material science, pharmacology, and analytical chemistry. As research continues to uncover new potential uses for this compound, its significance in both academic and industrial settings is expected to grow further.

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