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Ethyl 5-oxo-5H-thiazolo[3,2-a]pyriMidine-6-carboxylate is a chemical compound with the molecular formula C10H8N2O3S. It is a thiazole derivative that is often used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. ethyl 5-oxo-5H-thiazolo[3,2-a]pyriMidine-6-carboxylate has potential medicinal properties, including antifungal and antibacterial activities, and is being studied for its potential use in the treatment of various diseases. Ethyl 5-oxo-5H-thiazolo[3,2-a]pyriMidine-6-carboxylate is often used as a building block in organic synthesis and plays an important role in the development of new drugs and biologically active compounds.

32278-52-7

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32278-52-7 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 5-oxo-5H-thiazolo[3,2-a]pyriMidine-6-carboxylate is used as an intermediate in the synthesis of pharmaceuticals for its potential medicinal properties, including antifungal and antibacterial activities. It contributes to the development of new drugs and biologically active compounds that can be used in the treatment of various diseases.
Used in Agrochemical Industry:
Ethyl 5-oxo-5H-thiazolo[3,2-a]pyriMidine-6-carboxylate is used as an intermediate in the synthesis of agrochemicals, where its antifungal and antibacterial properties can be utilized for the development of pesticides and other agricultural products to protect crops and enhance yield.
Used in Organic Synthesis:
Ethyl 5-oxo-5H-thiazolo[3,2-a]pyriMidine-6-carboxylate is used as a building block in organic synthesis, enabling the creation of a wide range of chemical compounds with diverse applications in various industries, including pharmaceuticals, agrochemicals, and materials science. Its versatility as a synthetic intermediate allows for the exploration of novel chemical entities with potential applications in medicine, agriculture, and other fields.

Check Digit Verification of cas no

The CAS Registry Mumber 32278-52-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,2,7 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 32278-52:
(7*3)+(6*2)+(5*2)+(4*7)+(3*8)+(2*5)+(1*2)=107
107 % 10 = 7
So 32278-52-7 is a valid CAS Registry Number.
InChI:InChI=1S/C9H8N2O3S/c1-2-14-8(13)6-5-10-9-11(7(6)12)3-4-15-9/h3-5H,2H2,1H3

32278-52-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 5-oxo-[1,3]thiazolo[3,2-a]pyrimidine-6-carboxylate

1.2 Other means of identification

Product number -
Other names 5-Oxo-5H-thiazolo<3,2-a>pyrimidin-6-carbonsaeure-aethylester

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:32278-52-7 SDS

32278-52-7Relevant academic research and scientific papers

Synthesis of Fused Pyrimidinone and Quinolone Derivatives in an Automated High-Temperature and High-Pressure Flow Reactor

Tsoung, Jennifer,Bogdan, Andrew R.,Kantor, Stanislaw,Wang, Ying,Charaschanya, Manwika,Djuric, Stevan W.

, p. 1073 - 1084 (2018/06/18)

Fused pyrimidinone and quinolone derivatives that are of potential interest to pharmaceutical research were synthesized within minutes in up to 96% yield in an automated Phoenix high-temperature and high-pressure continuous flow reactor. Heterocyclic scaffolds that are either hard to synthesize or require multisteps are readily accessible using a common set of reaction conditions. The use of low-boiling solvents along with the high conversions of these reactions allowed for facile workup and isolation. The methods reported herein are highly amenable for fast and efficient heterocycle synthesis as well as compound scale-ups.

Penicillins

-

, (2008/06/13)

A class of α-(heterocyclic carbonylamino) penicillins in which the heterocyclic group of the acyl moiety is a fused bicyclic ring having a nitrogen atom at the bridge position, shows good antibacterial activity.

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