Cas no 1253790-16-7 (tert-Butyl (3-amino-3-methylbutyl)carbamate hydrochloride)

Technical Introduction: tert-Butyl (3-amino-3-methylbutyl)carbamate hydrochloride is a protected amine derivative widely used in organic synthesis and pharmaceutical research. The tert-butyloxycarbonyl (Boc) group provides stability under basic conditions while allowing selective deprotection under acidic conditions, making it valuable for peptide and intermediate synthesis. The hydrochloride salt enhances solubility and handling in polar solvents. Its rigid 3-methylbutyl backbone contributes to steric control in reactions, improving selectivity. This compound is particularly useful in the preparation of bioactive molecules, where controlled amine reactivity is required. High purity and consistent performance make it a reliable choice for complex synthetic applications.
tert-Butyl (3-amino-3-methylbutyl)carbamate hydrochloride structure
1253790-16-7 structure
Product Name:tert-Butyl (3-amino-3-methylbutyl)carbamate hydrochloride
CAS No:1253790-16-7
MF:C10H23ClN2O2
MW:238.754822015762
MDL:MFCD16295146
CID:1036709
PubChem ID:53422669
Update Time:2025-10-29

tert-Butyl (3-amino-3-methylbutyl)carbamate hydrochloride Chemical and Physical Properties

Names and Identifiers

    • tert-Butyl (3-amino-3-methylbutyl)carbamate hydrochloride
    • 1-N-Boc-3-Methylbutane-1,3-diaMine HCl
    • YEVUZCQMURNMQB-UHFFFAOYSA-N
    • SB39328
    • I11631
    • tert-butyl (3-amino-3-methylbutyl)carbamate HCl
    • (3-Amino-3-methyl-butyl)-carbamic acid tert-butyl ester hydrochloride
    • SCHEMBL2523548
    • tert-Butyl(3-amino-3-methylbutyl)carbamatehydrochloride
    • AKOS015923396
    • 1-N-Boc-3-Methylbutane-1,3-diamine hydrochloride
    • DA-46683
    • 1-N-Boc-3-methylbutane-1,3-diamine-HCl
    • 1253790-16-7
    • tert-butyl N-(3-amino-3-methylbutyl)carbamate;hydrochloride
    • Carbamic acid, N-(3-amino-3-methylbutyl)-, 1,1-dimethylethyl ester, hydrochloride (1:1)
    • 1-N-Boc-3-methylbutanel-1,3-diamine
    • MDL: MFCD16295146
    • Inchi: 1S/C10H22N2O2.ClH/c1-9(2,3)14-8(13)12-7-6-10(4,5)11;/h6-7,11H2,1-5H3,(H,12,13);1H
    • InChI Key: YEVUZCQMURNMQB-UHFFFAOYSA-N
    • SMILES: Cl.O(C(NCCC(C)(C)N)=O)C(C)(C)C

Computed Properties

  • Exact Mass: 238.1448057g/mol
  • Monoisotopic Mass: 238.1448057g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 6
  • Complexity: 195
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 64.4?2

tert-Butyl (3-amino-3-methylbutyl)carbamate hydrochloride Pricemore >>

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tert-Butyl (3-amino-3-methylbutyl)carbamate hydrochloride Related Literature

Additional information on tert-Butyl (3-amino-3-methylbutyl)carbamate hydrochloride

Introduction to Tert-Butyl (3-Amino-3-Methylbutyl)Carbamate Hydrochloride (CAS No. 1253790-16-7)

Ter-t-butyl (3-amino-3-methylbutyl)carbamate hydrochloride, with the chemical formula CAS No. 1253790-16-7, is a compound of significant interest in the field of pharmaceutical chemistry and biochemistry. This compound, characterized by its unique structural and functional properties, has garnered attention for its potential applications in drug development and molecular research. The tert-butyl moiety and the carbamate group contribute to its distinctive chemical behavior, making it a valuable candidate for various biochemical interactions.

The synthesis and characterization of this compound involve meticulous attention to detail, ensuring that its purity and stability are maintained for optimal performance in experimental settings. The hydrochloride salt form enhances its solubility in aqueous solutions, facilitating its use in a wide range of biological assays and pharmaceutical formulations. Recent advancements in synthetic methodologies have enabled more efficient production processes, allowing researchers to explore its applications more extensively.

In the realm of drug discovery, tert-butyl (3-amino-3-methylbutyl)carbamate hydrochloride has been investigated for its potential role as an intermediate in the synthesis of more complex pharmacophores. Its structural features make it a versatile building block for designing molecules with specific biological activities. For instance, the presence of both amino and carbamate functional groups allows for further derivatization, enabling the creation of novel compounds with enhanced therapeutic properties.

Recent studies have highlighted the compound's significance in medicinal chemistry. Researchers have explored its interactions with various biological targets, including enzymes and receptors, to understand its pharmacological profile. These investigations have revealed promising results regarding its potential as an inhibitor or modulator in certain therapeutic contexts. The compound's ability to engage with biological systems at multiple levels makes it a compelling subject for further research.

The development of new synthetic routes has also contributed to a deeper understanding of tert-butyl (3-amino-3-methylbutyl)carbamate hydrochloride's reactivity and stability. Advanced computational methods have been employed to predict and optimize reaction conditions, leading to more efficient and scalable synthesis protocols. These advancements not only improve the accessibility of the compound but also enhance the precision of experimental designs involving this molecule.

In addition to its synthetic utility, this compound has shown promise in preclinical studies as a component of multifunctional drug candidates. Its incorporation into drug formulations has been explored for enhancing bioavailability and targeting specific disease pathways. The combination of structural flexibility and functional diversity makes it an attractive candidate for developing next-generation therapeutics.

The role of tert-butyl (3-amino-3-methylbutyl)carbamate hydrochloride in biochemical research extends beyond drug development. It serves as a valuable tool for studying enzyme mechanisms and metabolic pathways. By interacting with key biological molecules, this compound provides insights into fundamental biochemical processes, contributing to our understanding of disease mechanisms and potential therapeutic interventions.

The future prospects of this compound are vast, with ongoing research aimed at uncovering new applications and refining existing methodologies. Collaborative efforts between academia and industry are expected to drive innovation, leading to novel derivatives and formulations with improved efficacy and safety profiles. As our knowledge of biochemical interactions grows, so too will the utility of tert-butyl (3-amino-3-methylbutyl)carbamate hydrochloride in advancing scientific discovery.

In conclusion, tert-butyl (3-amino-3-methylbutyl)carbamate hydrochloride represents a significant advancement in pharmaceutical chemistry and biochemistry. Its unique structural features, combined with its versatility in synthetic applications, make it a cornerstone in the development of new drugs and research tools. As research continues to evolve, this compound is poised to play an increasingly important role in addressing complex biological challenges and improving human health.

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