Cas no 37682-31-8 (Ethyl 2-(2-nitrophenoxy)acetate)

Ethyl 2-(2-nitrophenoxy)acetate structure
37682-31-8 structure
Product Name:Ethyl 2-(2-nitrophenoxy)acetate
CAS No:37682-31-8
MF:C10H11NO5
MW:225.198043107986
MDL:MFCD00100679
CID:1485167
PubChem ID:591948
Update Time:2025-04-23

Ethyl 2-(2-nitrophenoxy)acetate Chemical and Physical Properties

Names and Identifiers

    • Acetic acid, (2-nitrophenoxy)-, ethyl ester
    • ETHYL 2-(2-NITROPHENOXY)ACETATE
    • 2-(2-Nitro-phenoxy)acetic acid ethyl ester
    • SCHEMBL13099833
    • F94736
    • 37682-31-8
    • ULWPSRBTOBHBKT-UHFFFAOYSA-N
    • Ethyl (2-nitrophenoxy)acetate #
    • Acetic acid, 2-(2-nitrophenoxy)-, ethyl ester
    • DTXSID80343745
    • 4D-011
    • STK434804
    • MFCD00100679
    • Oprea1_866421
    • AKOS003294124
    • CS-0206674
    • J-505682
    • ethyl 2-(2'-nitrophenoxy)acetate
    • Ethyl (2-nitrophenoxy)acetate
    • ethyl2-(2-nitrophenoxy)acetate
    • Ethyl 2-(2-nitrophenoxy)acetate
    • MDL: MFCD00100679
    • Inchi: 1S/C10H11NO5/c1-2-15-10(12)7-16-9-6-4-3-5-8(9)11(13)14/h3-6H,2,7H2,1H3
    • InChI Key: ULWPSRBTOBHBKT-UHFFFAOYSA-N
    • SMILES: O(CC(=O)OCC)C1C=CC=CC=1[N+](=O)[O-]

Computed Properties

  • Exact Mass: 225.06373
  • Monoisotopic Mass: 225.06372245g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 6
  • Complexity: 250
  • 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: 1.7
  • Topological Polar Surface Area: 81.4?2

Experimental Properties

  • PSA: 78.67

Ethyl 2-(2-nitrophenoxy)acetate Pricemore >>

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Additional information on Ethyl 2-(2-nitrophenoxy)acetate

Acetic acid, (2-nitrophenoxy)-, ethyl ester: A Comprehensive Overview

The compound Acetic acid, (2-nitrophenoxy)-, ethyl ester (CAS NO37682-31-8) is a specialized organic compound that has garnered attention in various fields of scientific research. This compound belongs to the class of esters derived from acetic acid and features a unique functional group: 2-nitrophenoxy. Its structure and properties make it an interesting subject for exploration in areas such as pharmacology, agriculture, and materials science.

Acetic acid derivatives are widely studied due to their versatile chemical properties and potential applications. The presence of the nitrophenoxy group introduces additional reactivity and functionality, making this compound a valuable material for researchers. Recent studies have highlighted its potential in medicinal chemistry as a precursor for more complex molecules or as a bioisostere in drug development.

One of the key features of Acetic acid, (2-nitrophenoxy)-, ethyl ester is its stability under certain reaction conditions. This makes it an ideal candidate for use in organic synthesis, where maintaining structural integrity during reactions is crucial. Additionally, its solubility characteristics and ability to form stable intermediates have been explored in the context of green chemistry.

Recent advancements in drug delivery systems have also considered this compound as a potential building block for controlled release formulations. The ester group can be engineered to release the active moiety at a controlled rate, offering promising applications in sustained drug delivery mechanisms.

In the realm of agricultural chemistry, this compound has shown promise as a candidate for herbicide or pesticide development. Its ability to interact with plant systems and disrupt essential biochemical pathways could lead to innovative solutions for weed control or pest management.

Furthermore, the 2-nitrophenoxy group introduces electronic effects that can modulate the pharmacokinetics of molecules derived from this compound. This has implications in drug design, particularly in improving absorption, distribution, metabolism, and excretion (ADME) properties.

Recent research has also explored the potential of Acetic acid, (2-nitrophenoxy)-, ethyl ester in polymer synthesis. Its functional groups can serve as linking agents or cross-linking agents in the formation of biodegradable polymers, which are increasingly sought after for environmentally friendly applications.

The study of this compound aligns with current trends in precision medicine, where tailored therapeutic solutions are developed based on individual genetic profiles. Its modular structure allows for easy modification to create molecule libraries that can be screened for desired biological activities.

Given its unique properties, Acetic acid, (2-nitrophenoxy)-, ethyl ester serves as a valuable tool in the arsenal of modern chemical research. Its applications span multiple disciplines, and ongoing investigations promise to uncover new avenues for its utilization in both academic and industrial settings.

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