Cas no 942308-05-6 (tert-Butyl 3-(methoxymethyl)azetidine-1-carboxylate)

Technical Introduction: tert-Butyl 3-(methoxymethyl)azetidine-1-carboxylate is a protected azetidine 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 stepwise functionalization. The methoxymethyl substituent enhances solubility and reactivity, facilitating further modifications. This compound serves as a versatile intermediate in the synthesis of complex molecules, particularly in the development of bioactive compounds and heterocyclic scaffolds. Its well-defined reactivity and compatibility with diverse reaction conditions make it a preferred choice for medicinal chemistry and materials science applications. Storage under inert conditions is recommended to maintain stability.
tert-Butyl 3-(methoxymethyl)azetidine-1-carboxylate structure
942308-05-6 structure
Product Name:tert-Butyl 3-(methoxymethyl)azetidine-1-carboxylate
CAS No:942308-05-6
MF:C10H19NO3
MW:201.262763261795
MDL:MFCD09752649
CID:1024806
PubChem ID:66570673
Update Time:2025-10-20

tert-Butyl 3-(methoxymethyl)azetidine-1-carboxylate Chemical and Physical Properties

Names and Identifiers

    • tert-Butyl 3-(methoxymethyl)azetidine-1-carboxylate
    • 1-(tert-butoxycarbonyl)-3-methoxymethylazetidine
    • SB50740
    • MFCD09752649
    • KVZWHTCHJHENKO-UHFFFAOYSA-N
    • AS-35606
    • A859500
    • SCHEMBL71546
    • DTXSID50735279
    • 3-Methoxymethyl-azetidine-1-carboxylic acid tert-butyl ester
    • EN300-7296038
    • AKOS015999289
    • 1-BOC-3-(METHOXYMETHYL)AZETIDINE
    • CS-0079189
    • tert-Butyl3-(methoxymethyl)azetidine-1-carboxylate
    • 942308-05-6
    • DB-311241
    • MDL: MFCD09752649
    • Inchi: 1S/C10H19NO3/c1-10(2,3)14-9(12)11-5-8(6-11)7-13-4/h8H,5-7H2,1-4H3
    • InChI Key: KVZWHTCHJHENKO-UHFFFAOYSA-N
    • SMILES: O(C(C)(C)C)C(N1CC(COC)C1)=O

Computed Properties

  • Exact Mass: 201.13649347g/mol
  • Monoisotopic Mass: 201.13649347g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 5
  • Complexity: 204
  • 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
  • Topological Polar Surface Area: 38.8?2

Experimental Properties

  • Color/Form: Liquid
  • Density: 1.0±0.1 g/cm3
  • Boiling Point: 247.7±13.0 °C at 760 mmHg
  • Flash Point: 103.6±19.8 °C
  • Vapor Pressure: 0.0±0.5 mmHg at 25°C

tert-Butyl 3-(methoxymethyl)azetidine-1-carboxylate Security Information

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Additional information on tert-Butyl 3-(methoxymethyl)azetidine-1-carboxylate

tert-Butyl 3-(methoxymethyl)azetidine-1-carboxylate: A Comprehensive Overview

The compound tert-butyl 3-(methoxymethyl)azetidine-1-carboxylate, identified by the CAS number 942308-05-6, is a significant molecule in the field of organic chemistry and pharmaceutical research. This compound belongs to the class of azetidines, which are four-membered ring structures with one nitrogen atom. The presence of the tert-butyl group and the methoxymethyl substituent introduces unique chemical properties, making it a versatile building block for various applications.

Recent studies have highlighted the potential of tert-butyl 3-(methoxymethyl)azetidine-1-carboxylate in drug delivery systems. Its ability to form stable complexes with bioactive molecules has been explored in nanotechnology-based drug delivery platforms. Researchers have demonstrated that this compound can enhance the solubility and bioavailability of poorly soluble drugs, making it a promising candidate for improving therapeutic outcomes.

In terms of synthesis, tert-butyl 3-(methoxymethyl)azetidine-1-carboxylate is typically prepared through a multi-step process involving nucleophilic substitution and ring-closing reactions. The use of environmentally friendly catalysts has been reported in recent publications, aligning with the growing emphasis on sustainable chemical synthesis. These advancements not only improve the efficiency of production but also reduce the environmental footprint associated with its manufacturing.

The chemical stability of tert-butyl 3-(methoxymethyl)azetidine-1-carboxylate under various conditions has been extensively studied. Research indicates that it exhibits excellent thermal stability, making it suitable for high-temperature applications. Additionally, its resistance to hydrolysis under physiological conditions suggests potential use in long-term drug delivery systems.

In the pharmaceutical industry, this compound has shown promise as an intermediate in the synthesis of complex molecules. Its role as a precursor in the development of novel antibiotics and antiviral agents has been documented in recent scientific journals. The ability to modify its structure further enhances its utility in creating customized drug molecules tailored to specific therapeutic needs.

The application of tert-butyl 3-(methoxymethyl)azetidine-1-carboxylate extends beyond pharmaceuticals into materials science. Its incorporation into polymer formulations has been explored for developing biocompatible materials used in medical devices and implants. The compound's compatibility with biological systems makes it an attractive option for such applications.

From an environmental perspective, studies have focused on the biodegradation potential of tert-butyl 3-(methoxymethyl)azetidine-1-carboxylate. Findings suggest that under aerobic conditions, it undergoes efficient microbial degradation, minimizing its persistence in natural ecosystems. This attribute is crucial for ensuring its safe use in both industrial and biomedical applications.

In conclusion, tert-butyl 3-(methoxymethyl)azetidine-1-carboxylate stands out as a multifaceted compound with diverse applications across various scientific domains. Its unique chemical properties, coupled with recent advancements in synthesis and application techniques, position it as a key player in future innovations within organic chemistry and pharmaceutical research.

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