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(3-Aminopyrazol-4-yl)(2-thienyl)methanone is a chemical compound that belongs to the classes of aminopyrazoles and thiophenes. It is characterized by its molecular formula C9H8N2OS and features a pyrazole ring, a heterocyclic aromatic organic compound. (3-AMINOPYRAZOL-4-YL)(2-THIENYL)METHANONE has a role as a phosphodiesterase 5 inhibitor and generally appears as a solid. Its unique structural characteristics and properties make it suitable for various chemical reactions and processes. However, there is limited information available on its potential risks, indicating a need for more comprehensive studies on its properties, effects, and potential hazards.

96219-87-3

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96219-87-3 Usage

Uses

Used in Pharmaceutical Industry:
(3-Aminopyrazol-4-yl)(2-thienyl)methanone is used as a phosphodiesterase 5 inhibitor for the development of drugs targeting various medical conditions. Its role in inhibiting phosphodiesterase 5 can lead to increased levels of cyclic guanosine monophosphate (cGMP), which is involved in the regulation of smooth muscle relaxation and blood flow. This property makes it a promising candidate for the treatment of conditions such as erectile dysfunction, pulmonary arterial hypertension, and other cardiovascular diseases.
Used in Chemical Research:
(3-Aminopyrazol-4-yl)(2-thienyl)methanone is used as a research compound in the field of organic chemistry. Its unique structural characteristics, including the presence of a pyrazole ring, make it a valuable subject for studying the reactivity and properties of heterocyclic compounds. Researchers can use (3-AMINOPYRAZOL-4-YL)(2-THIENYL)METHANONE to explore new synthetic routes, reaction mechanisms, and potential applications in various chemical processes.
Used in Material Science:
(3-Aminopyrazol-4-yl)(2-thienyl)methanone can be used as a building block or intermediate in the synthesis of various materials with specific properties. Its structural features, such as the presence of a pyrazole ring and a thienyl group, can contribute to the development of new materials with potential applications in areas such as electronics, sensors, and energy storage.

Check Digit Verification of cas no

The CAS Registry Mumber 96219-87-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,1 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 96219-87:
(7*9)+(6*6)+(5*2)+(4*1)+(3*9)+(2*8)+(1*7)=163
163 % 10 = 3
So 96219-87-3 is a valid CAS Registry Number.

96219-87-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-amino-1H-pyrazol-4-yl)-thiophen-2-ylmethanone

1.2 Other means of identification

Product number -
Other names -

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:96219-87-3 SDS

96219-87-3Relevant academic research and scientific papers

Salts And Co-Crystals of Pyrazolopyrimidine Compounds, Compositions Thereof And Methods For Their Production And Use

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Page/Page column 10, (2010/11/30)

The invention provides pharmaceutically acceptable salts and co-crystals of pyrazolopyrimidine compounds such as zaleplon, indiplon and ocinaplon, processes for their preparation, compositions comprising such salts and co-crystals and methods of using such salts and co-crystals for treating various diseases and conditions.

NOVEL HETEROBICYCLIC COMPOUNDS

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Page/Page column 42, (2010/11/29)

This invention relates to novel pyrazolo-pyrimidine compounds and their use as analytical tools and in methods of treating neurological disorders, including sleep disorders such as insomnia.

Pyrazolo[1,5-a]pyrimidin-7-yl phenyl amides as novel antiproliferative agents: Exploration of core and headpiece structure-activity relationships

Powell, Dennis,Gopalsamy, Ariamala,Wang, Yanong D.,Zhang, Nan,Miranda, Miriam,McGinnis, John P.,Rabindran, Sridhar K.

, p. 1641 - 1645 (2007/10/03)

A novel series of antiproliferative agents containing pyrazolo[1,5-a]pyrimidin-7-yl phenyl amides, selective for p21-deficient cells, were identified by high-throughput screening. Exploration of the SAR relationships in the headpiece, core, and tailpiece

Method of using substituted pyrazolo [1,5-a] pyrimidines

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Page/Page column 45, (2010/10/20)

This invention relates to novel methods of use of certain pyrazolo[1,5-a]pyrimidine compounds and the therapeutically acceptable salts thereof. This invention also relates to novel methods of using these compounds as anti-proliferative agents in mammals, including humans.

Substituted pyrazolo[1,5-a] pyrimidines and process for making same

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Page/Page column 50, (2010/10/20)

This invention relates to novel pyrazolo[1,5-a]pyrimidine compounds and the therapeutically acceptable salts thereof. These compounds are useful as anti-proliferative agents in mammals, including humans.

Pyrazolo[1,5-a]pyrimidin-7-yl phenyl amides as novel anti-proliferative agents: Parallel synthesis for lead optimization of amide region

Gopalsamy, Ariamala,Yang, Hui,Ellingboe, John W.,Tsou, Hwei-Ru,Zhang, Nan,Honores, Erick,Powell, Dennis,Miranda, Miriam,McGinnis, John P.,Rabindran, Sridhar K.

, p. 1591 - 1594 (2007/10/03)

A novel series of p21 chemoselective agents containing a pyrazolo[1,5-a]pyrimidin-7-yl phenyl amides were identified by high throughput screening. Optimization of the amide region by parallel synthesis and the iterative design toward understanding structu

N-methyl-N-(3-{3-[2-thienylcarbonyl]-pyrazol-[1, 5-α]-pyrimidin-7-yl}phenyl)acetamide and compositions and methods related thereto

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, (2008/06/13)

N-methyl-N-(3-{3-[2-thienylcarbonyl]-pyrazol-[1,5-α]-pyrimidin-7-yl}phenyl)acetamide, and use of the same as a sedative-hypnotic, anxiolytic, anticonvulsant, and skeletal muscle relaxant agent. Compositions containing N-methyl-N-(3-{3-[2-thienylcarbonyl]-pyrazol-[1,5-α]-pyrimidin-7-yl}phenyl)acetamide, as well as pharmaceutically acceptable salts thereof, are also disclosed.

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