4701-93-3 Usage
Uses
Used in Pharmaceutical Synthesis:
(2E)-N-hydroxybicyclo[4.1.0]heptan-2-imine is used as a key intermediate for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of complex organic molecules that can be utilized in the development of new drugs.
Used in Agrochemical Production:
In the agrochemical industry, (2E)-N-hydroxybicyclo[4.1.0]heptan-2-imine serves as an essential building block for the production of various agrochemicals. Its role in the synthesis of these compounds contributes to the development of effective products for agricultural applications.
Used in Specialty Chemicals Synthesis:
(2E)-N-hydroxybicyclo[4.1.0]heptan-2-imine is used as a versatile intermediate in the synthesis of specialty chemicals. Its ability to participate in a range of chemical reactions makes it a valuable component in the production of specialized chemical products.
Used in Polymer Production:
(2E)-N-hydroxybicyclo[4.1.0]heptan-2-imine is also used in the production of polymers. Its chemical properties allow it to be integrated into polymer structures, potentially enhancing their performance and expanding their applications.
Used in Catalysis:
(2E)-N-hydroxybicyclo[4.1.0]heptan-2-imine has been studied for its potential applications in catalysis. Its ability to facilitate various chemical reactions makes it a candidate for use in catalytic processes to improve efficiency and selectivity.
Used as a Chiral Auxiliary in Asymmetric Synthesis:
In asymmetric synthesis, (2E)-N-hydroxybicyclo[4.1.0]heptan-2-imine is used as a chiral auxiliary. Its stereochemistry aids in the selective formation of desired enantiomers, which is crucial in the production of enantiomerically pure compounds, especially in the pharmaceutical industry.
Used in Organic Chemistry Research:
(2E)-N-hydroxybicyclo[4.1.0]heptan-2-imine is a valuable compound in organic chemistry research. Its ability to undergo reactions such as cycloadditions and hydrogenations makes it an important subject of study for understanding and developing new synthetic methods and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 4701-93-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4701-93:
(6*4)+(5*7)+(4*0)+(3*1)+(2*9)+(1*3)=83
83 % 10 = 3
So 4701-93-3 is a valid CAS Registry Number.
4701-93-3Relevant academic research and scientific papers
The crocacins: Novel natural products as leads for agricultural fungicides
Crowley, Patrick J.,Aspinall, Ian H.,Gillen, Kevin,Godfrey, Christopher R.A.,Devillers, Ingrid M.,Munns, Gordon R.,Sageot, Olivia-Anabelle,Swanborough, Joe,Worthington, Paul A.,Williams, John
, p. 685 - 691 (2007/10/03)
A short route to the synthesis of analogues of the antifungal but unstable natural product crocacin D was developed. A wide range of compounds were made in which the complex side chain was replaced by simple aromatic units, and many of them showed high activity in a mitochondrial beef heart respiration assay. Some of these compounds were active against plant pathogenic fungi of agricultural importance in glasshouse tests. In order to find compounds with greater stability than the natural crocacins, the photolabile (Z)-enamide was replaced with many different moieties, but none gave rise to useful fungicidal activity.
Synthesis of gem-dinitro compounds with a three-membered cycle
Moiseev,Mratkhuzina,Balenkova,Makarova
, p. 839 - 840 (2007/10/03)
A reaction was studied between nitrogen pentoxide in chloroform and oximes of cyclic ketones, derivatives of bicyclo[3.1.0]hexane, bicyclo[4.1.0]heptane, spiro[2.4]heptane, spiro[2.5]octane, resulting in the corresponding gem-dinitro compounds.
