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Ethyl 4,7-dihydro-7-oxopyrazolo[1,5-a]pyrimidine-3-carboxylate is a pyrazolo[1,5-a]pyrimidine derivative with the molecular formula C9H10N4O3. It is a chemical compound that is widely used in organic synthesis and medicinal chemistry due to its potential pharmacological properties. Ethyl 4,7-dihydro-7-oxopyrazolo[1,5-a]pyrimidine-3-carboxylate has been studied for its potential use in the development of new drugs and has demonstrated biological activities such as antitumor and anti-inflammatory properties. Its versatile structure makes it a promising candidate for the design and development of novel pharmaceutical agents.

104556-86-7

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104556-86-7 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 4,7-dihydro-7-oxopyrazolo[1,5-a]pyrimidine-3-carboxylate is used as a key intermediate in the synthesis of various pharmaceutical agents for its potential pharmacological properties. Its unique structure allows for the development of new drugs with improved therapeutic effects and reduced side effects.
Used in Medicinal Chemistry Research:
Ethyl 4,7-dihydro-7-oxopyrazolo[1,5-a]pyrimidine-3-carboxylate is used as a research compound in medicinal chemistry to explore its potential applications in drug discovery. Its biological activities, such as antitumor and anti-inflammatory properties, make it a valuable tool for studying the mechanisms of action and developing new therapeutic agents.
Used in Organic Synthesis:
Ethyl 4,7-dihydro-7-oxopyrazolo[1,5-a]pyrimidine-3-carboxylate is used as a versatile building block in organic synthesis. Its chemical properties allow for the formation of various derivatives, which can be further modified to create new compounds with potential applications in different fields, including pharmaceuticals, agrochemicals, and materials science.
Used in Drug Design and Development:
Ethyl 4,7-dihydro-7-oxopyrazolo[1,5-a]pyrimidine-3-carboxylate is used as a starting material in the design and development of novel pharmaceutical agents. Its unique structure and biological activities provide a foundation for creating new drugs with improved efficacy, selectivity, and safety profiles. Researchers can utilize Ethyl 4,7-dihydro-7-oxopyrazolo[1,5-a]pyrimidine-3-carboxylate to explore new chemical spaces and identify potential drug candidates for various therapeutic areas.

Check Digit Verification of cas no

The CAS Registry Mumber 104556-86-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,5,5 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104556-86:
(8*1)+(7*0)+(6*4)+(5*5)+(4*5)+(3*6)+(2*8)+(1*6)=117
117 % 10 = 7
So 104556-86-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H9N3O3/c1-2-15-9(14)6-5-11-12-7(13)3-4-10-8(6)12/h3-5,10H,2H2,1H3

104556-86-7SDS

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 Ethyl 4,7-dihydro-7-oxopyrazolo[1,5-a]pyrimidine-3-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl succinyl chloride(ESC)

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 -
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More Details:104556-86-7 SDS

104556-86-7Downstream Products

104556-86-7Relevant academic research and scientific papers

Synthesis of pyrazolo[1,5-α]pyrimidinone regioisomers

Gavrin, Lori K.,Lee, Arthur,Provencher, Brian A.,Massefski, Walter W.,Huhn, Stephen D.,Ciszewski, Gregory M.,Cole, Derek C.,McKew, John C.

, p. 1043 - 1046 (2008/02/04)

(Chemical Equation Presented) This work describes two distinct routes to prepare pyrazolo-[1,5-α]pyrimidin-7-ones and two distinct routes to prepare pyrazolo[1,5-α]pyrimidin-5-ones. Use of 1,3-dimethyluracil as the electrophile in the preparation of the p

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