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899809-61-1

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899809-61-1 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.

Check Digit Verification of cas no

The CAS Registry Mumber 899809-61-1 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 899809-61:
(8*8)+(7*9)+(6*9)+(5*8)+(4*0)+(3*9)+(2*6)+(1*1)=261
261 % 10 = 1
So 899809-61-1 is a valid CAS Registry Number.

899809-61-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-4-Hydroxy-N,N-diphenylpent-2-ynamide

1.2 Other means of identification

Product number -
Other names 4-HYDROXY-N,N-DIPHENYL (4R)-2-PENTYNAMIDE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:899809-61-1 SDS

899809-61-1Relevant articles and documents

Thrombin Receptor Antagonists Based On The Modified Tricyclic Unit Of Himbacine

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Page/Page column 29, (2008/06/13)

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

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Page/Page column 27; 28, (2008/06/13)

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

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