899809-64-4 Usage
Uses
Used in Organic Synthesis:
2-Propenoic acid, 3-(5-nitro-1-cyclohexen-1-yl)-, (2E)is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure and functional groups make it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-Propenoic acid, 3-(5-nitro-1-cyclohexen-1-yl)-, (2E)is utilized as a starting material or a key intermediate in the development of new drugs. Its potential biological activities and reactivity make it a promising candidate for the discovery of novel therapeutic agents. Researchers can exploit its unique structural features to design and synthesize compounds with specific pharmacological properties.
Used in Medicinal Chemistry:
2-Propenoic acid, 3-(5-nitro-1-cyclohexen-1-yl)-, (2E)is employed in medicinal chemistry for the design and optimization of drug candidates. Its presence of the 5-nitro-1-cyclohexen-1-yl group may confer specific biological activities, such as nitroaromatic or cyclohexenyl reactivity, which can be harnessed to modulate the pharmacological properties of the resulting compounds. This allows researchers to explore new avenues for drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 899809-64-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,9,8,0 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 899809-64:
(8*8)+(7*9)+(6*9)+(5*8)+(4*0)+(3*9)+(2*6)+(1*4)=264
264 % 10 = 4
So 899809-64-4 is a valid CAS Registry Number.
899809-64-4Relevant academic research and scientific papers
Synthesis of 3-(5-nitrocyclohex-1-enyl) acrylic acid and esters thereof
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Page/Page column 12, (2008/06/13)
This application discloses provides a process for the introduction of nitro-group functionality into a compound which contains also a site of unsaturation and/or oxygen functionality by direct (one step) oxidation of an oxime functional group mediated by
EXO- AND DIASTEREO- SELECTIVE SYNTHESES OF HIMBACINE ANALOGS
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Page/Page column 35-37, (2008/06/13)
The application discloses a novel process for the preparation of himbacine analogs useful as thrombin receptor antagonists. The process is based in part on the use of a base-promoted dynamic epimerization of a chiral nitro center. The chemistry taught her
PREPARATION OF CHIRAL PROPARGYLIC ALCOHOL AND ESTER INTERMEDIATES OF HIMBACINE ANALOGS
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Page/Page column 42-44, (2008/06/13)
This application discloses a novel process for the conversion of a series of racemic propargylic alcohols to corresponding (R)-enantiomers. The application also discloses the enantio-selective esterification of a propargylic alcohol from its racemate to p
