Cas no 158001-20-8 (Hydrazinecarboxylicacid, 2-cyclobutylidene-, 1,1-dimethylethyl ester)

Hydrazinecarboxylicacid, 2-cyclobutylidene-, 1,1-dimethylethyl ester structure
158001-20-8 structure
Product Name:Hydrazinecarboxylicacid, 2-cyclobutylidene-, 1,1-dimethylethyl ester
CAS No:158001-20-8
MF:C9H16N2O2
MW:184.235542297363
MDL:MFCD16620855
CID:107967
PubChem ID:45092398
Update Time:2025-11-01

Hydrazinecarboxylicacid, 2-cyclobutylidene-, 1,1-dimethylethyl ester Chemical and Physical Properties

Names and Identifiers

    • Hydrazinecarboxylicacid, 2-cyclobutylidene-, 1,1-dimethylethyl ester
    • N'-cyclobutylidene-hydrazinecarboxylic acid tert-butyl ester
    • TERT-BUTYL CYCLOBUTYLIDENECARBAZATE
    • tert-butyl2-cyclobutylidenehydrazine-1-carboxylate
    • tert-butyl 2-cyclobutylidenehydrazinecarboxylate(WX191453)
    • N-Cyclobutylidene-hydrazinecarboxylic acid tert-butyl ester
    • Hydrazinecarboxylic acid, cyclobutylidene-, 1,1-dimethylethyl ester (9CI)
    • AS-73096
    • tert-butyl 2-cyclobutylidenehydrazinecarboxylate
    • N'-cyclobutylidene(tert-butoxy)carbohydrazide
    • SCHEMBL272269
    • A921883
    • tert-butyl N-(cyclobutylideneamino)carbamate
    • tert-butyl2-cyclobutylidenehydrazinecarboxylate
    • 1-Boc-2-cyclobutylidenehydrazine
    • 158001-20-8
    • AKOS027252232
    • SY258920
    • AB6624
    • MFCD16620855
    • ZNFZQJAVXBBTCJ-UHFFFAOYSA-N
    • DB-160116
    • Tert-butyl 2-cyclobutylidenehydrazine-1-carboxylate
    • MDL: MFCD16620855
    • Inchi: 1S/C9H16N2O2/c1-9(2,3)13-8(12)11-10-7-5-4-6-7/h4-6H2,1-3H3,(H,11,12)
    • InChI Key: ZNFZQJAVXBBTCJ-UHFFFAOYSA-N
    • SMILES: O(C(N/N=C1\CCC\1)=O)C(C)(C)C

Computed Properties

  • Exact Mass: 184.12128
  • Monoisotopic Mass: 184.121177757g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 4
  • Complexity: 222
  • 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: 1.2
  • Topological Polar Surface Area: 50.7?2

Experimental Properties

  • PSA: 50.69

Hydrazinecarboxylicacid, 2-cyclobutylidene-, 1,1-dimethylethyl ester Pricemore >>

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Additional information on Hydrazinecarboxylicacid, 2-cyclobutylidene-, 1,1-dimethylethyl ester

Hydrazinecarboxylic Acid, 2-Cyclobutylidene-, 1,1-Dimethylethyl Ester (CAS No. 158001-20-8): An Overview

Hydrazinecarboxylic acid, 2-cyclobutylidene-, 1,1-dimethylethyl ester (CAS No. 158001-20-8) is a specialized organic compound that has garnered significant attention in the fields of chemical synthesis and pharmaceutical research. This compound, often referred to as a cyclobutylidene hydrazinecarboxylic acid ester, is characterized by its unique structural features and potential applications in various scientific domains.

The molecular structure of Hydrazinecarboxylic acid, 2-cyclobutylidene-, 1,1-dimethylethyl ester consists of a hydrazinecarboxylic acid moiety linked to a cyclobutylidene group and a tert-butyl ester. This combination provides the compound with distinct chemical properties, making it an intriguing subject for both academic and industrial research. The tert-butyl ester group, in particular, is known for its stability and ability to protect the carboxylic acid functionality during synthetic transformations.

Recent studies have highlighted the potential of Hydrazinecarboxylic acid, 2-cyclobutylidene-, 1,1-dimethylethyl ester in the development of novel pharmaceuticals. One notable application is in the synthesis of prodrugs, where the compound serves as a versatile intermediate. Prodrugs are biologically inactive compounds that are converted into their active forms within the body, often improving drug delivery and reducing side effects. The tert-butyl ester group in this compound can be selectively cleaved under specific conditions, releasing the active hydrazinecarboxylic acid derivative.

In addition to its role in prodrug synthesis, Hydrazinecarboxylic acid, 2-cyclobutylidene-, 1,1-dimethylethyl ester has shown promise in the field of medicinal chemistry. Researchers have explored its use as a building block for the synthesis of small molecules with potential therapeutic applications. For instance, studies have demonstrated that derivatives of this compound exhibit anti-inflammatory and anti-cancer properties. These findings suggest that further investigation into the biological activities of Hydrazinecarboxylic acid, 2-cyclobutylidene-, 1,1-dimethylethyl ester could lead to the development of new therapeutic agents.

The synthetic versatility of Hydrazinecarboxylic acid, 2-cyclobutylidene-, 1,1-dimethylethyl ester is another key aspect that has attracted attention from chemists and pharmaceutical scientists. The compound can be readily modified through various chemical reactions, such as nucleophilic substitution and coupling reactions. This flexibility allows for the creation of a wide range of derivatives with tailored properties, making it an attractive starting material for drug discovery programs.

In terms of safety and handling, it is important to note that while Hydrazinecarboxylic acid, 2-cyclobutylidene-, 1,1-dimethylethyl ester is not classified as a hazardous substance under current regulations, standard laboratory practices should be followed to ensure safe handling and storage. Proper personal protective equipment (PPE) should be used when working with this compound to minimize exposure risks.

The environmental impact of Hydrazinecarboxylic acid, 2-cyclobutylidene-, 1,1-dimethylethyl ester is also an important consideration. Research into the biodegradability and environmental fate of this compound is ongoing to ensure that its use does not pose significant ecological risks. Preliminary studies suggest that the compound is relatively stable under environmental conditions but can be degraded through microbial processes.

In conclusion, Hydrazinecarboxylic acid, 2-cyclobutylidene-, 1,1-dimethylethyl ester (CAS No. 158001-20-8) represents a valuable addition to the arsenal of organic compounds used in chemical synthesis and pharmaceutical research. Its unique structural features and versatile reactivity make it an attractive candidate for further exploration in both academic and industrial settings. As research continues to uncover new applications and properties of this compound, it is likely to play an increasingly important role in the development of innovative chemical and pharmaceutical products.

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