899809-61-1

Usage

Uses

Due to the lack of detailed information in the provided materials, the specific applications of 4-hydroxy-N,N-diphenyl-(4R)-2-Pentynamide cannot be accurately listed. However, based on its chemical structure and the general properties of similar compounds, some potential uses in various industries can be hypothesized:
Used in Pharmaceutical Industry:
4-Hydroxy-N,N-diphenyl-(4R)-2-Pentynamide could be used as an active pharmaceutical ingredient for the development of new drugs, given its complex molecular structure and functional groups. Its potential applications may include the treatment of various diseases or conditions, depending on its biological activity and pharmacological properties.
Used in Chemical Synthesis:
4-hydroxy-N,N-diphenyl-(4R)-2-Pentynamide may serve as a key intermediate or building block in the synthesis of other complex organic molecules, such as pharmaceuticals, agrochemicals, or specialty chemicals. Its unique structure and functional groups could be utilized in various chemical reactions to form new compounds with desired properties.
Used in Material Science:
4-Hydroxy-N,N-diphenyl-(4R)-2-Pentynamide might find applications in the development of new materials with specific properties, such as polymers, coatings, or adhesives. Its structural features and chemical reactivity could contribute to the creation of materials with improved performance characteristics.
Used in Research and Development:
Due to its complex structure and limited information available, 4-hydroxy-N,N-diphenyl-(4R)-2-Pentynamide could be a subject of interest for researchers in various fields, such as organic chemistry, medicinal chemistry, or materials science. It may be used as a model compound to study its properties, reactivity, and potential applications in different areas.

Upstream product

• 899833-36-4 C₁₉H₁₇NO₃ 
• 899809-73-5 C₁₉H₁₇NO₃ 
• 416844-85-4 C₇H₁₃LiOSi 
• 2875-79-8 N,N-diphenylimidazole-1-carboxamide 

Downstream Products

• 899809-77-9 C₂₄H₂₁NO₄S 
• 900160-96-5 (R,Z)-4-hydroxy-N,N-diphenylpent-2-enamide 
• 899809-60-0 C₂₆H₂₄N₂O₅ 
• 900161-11-7 C₂₉H₃₂N₂O₅ 
• 900161-12-8 C₂₉H₃₄N₂O₅ 

Relevant academic research and scientific papers

Thrombin Receptor Antagonists Based On The Modified Tricyclic Unit Of Himbacine

Multiple stereoisomers of the heterocyclic-substituted tricyclics of the formula: or a pharmaceutically acceptable salt, solvate, or ester of said compound wherein R and the stereochemistry are illustrated in the structural formulas herein are disclosed, as well as pharmaceutical compositions containing them and a method of treating diseases associated with thrombosis, atherosclerosis, restenosis, hypertension, angina pectoris, arrhythmia, heart failure, and cancer by administering said compounds. Combination therapy with other cardiovascular agents is also claimed.

PREPARATION OF CHIRAL PROPARGYLIC ALCOHOL AND ESTER INTERMEDIATES OF HIMBACINE ANALOGS

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

AN EXO-SELECTIVE SYNTHESIS OF HIMBACINE ANALOGS

This application discloses a novel process for the synthesis of himbacine analogs, as well as the compounds produced thereby. The synthesis proceeds by alternative routes including the cyclic ketal amide route, the chiral carbamate amide route, and the ch

EXO- AND DIASTEREO- SELECTIVE SYNTHESES OF HIMBACINE ANALOGS

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