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32278-52-7

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32278-52-7 Usage

General Description

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.

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 articles and documents

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.

Reaction of ethoxymethylenemalononitrile with 2 aminopyridines

Okamoto,Kurasawa,Takagi,et al.

, p. 243 - 247 (2007/10/08)

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