899809-61-1

Basic information

• Product Name: 4-hydroxy-N,N-diphenyl-(4R)-2-Pentynamide
• Synonyms: (R)-4-hydroxy-N,N-diphenylpent-2-ynaMide;4-Hydroxy-pent-2-ynoic acid diphenylamide;(4R)-4-Hydroxy-N,N-diphenyl-2-pentynamide;(4R)-4-hydroxy-N,N-diphenyl-2-pentyneamide;4-hydroxy-N,N-diphenyl-(4R)-2-Pentynamide
• CAS NO: 899809-61-1
• Molecular Formula: C₁₇H₁₅NO₂
• Molecular Weight: 265.3065
• Mol File: 899809-61-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 411.9±47.0 °C(Predicted)
• Appearance: /
• Density: 1 +-.0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 13.24±0.20(Predicted)
• CAS DataBase Reference: 4-hydroxy-N,N-diphenyl-(4R)-2-Pentynamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-hydroxy-N,N-diphenyl-(4R)-2-Pentynamide(899809-61-1)
• EPA Substance Registry System: 4-hydroxy-N,N-diphenyl-(4R)-2-Pentynamide(899809-61-1)

Safety Data

• Hazardous Substances Data: 899809-61-1(Hazardous Substances Data)

Usage

Description

4-Hydroxy-N,N-diphenyl-(4R)-2-Pentynamide is a complex organic chemical compound characterized by its unique molecular structure. It belongs to the family of anilides and phenylpropanoids, featuring a hydroxy group (-OH) attached to a benzene ring, two phenyl groups (-C6H5) connected to the nitrogen of an amide group, and a pentynyl group (-C2H3). The functionalities and applications of this compound are primarily determined by its chemical structure and behavior. However, specific information about its properties, uses, hazards, and handling procedures is not extensively available in public domains, suggesting that they may be industry-specific or less investigated.

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

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

Downstream Products

• 899809-76-8 C₁₈H₁₇NO₄S 
• 900160-96-5 (R,Z)-4-hydroxy-N,N-diphenylpent-2-enamide 
• 899809-60-0 C₂₆H₂₄N₂O₅ 
• 900161-12-8 C₂₉H₃₄N₂O₅ 
• 900161-11-7 C₂₉H₃₂N₂O₅ 

Relevant articles and documents

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.

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