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32084-55-2

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32084-55-2 Usage

Description

5-OXO-2,3-DIHYDRO-5H-PYRIMIDO[2,1-B][1,3]THIAZOLE-6-CARBOXYLIC ACID is a heterocyclic chemical compound characterized by a pyrimidine ring fused with a thiazole ring and a carboxylic acid functional group. As a ketone, it is denoted by the "5-OXO" prefix in its name. 5-OXO-2,3-DIHYDRO-5H-PYRIMIDO[2,1-B][1,3]THIAZOLE-6-CARBOXYLIC ACID's complex molecular structure and unique properties may offer potential applications in various fields, such as pharmaceuticals and agriculture, although further research is required to explore its specific uses and effects.

Uses

Used in Pharmaceutical Industry:
5-OXO-2,3-DIHYDRO-5H-PYRIMIDO[2,1-B][1,3]THIAZOLE-6-CARBOXYLIC ACID is used as a potential active pharmaceutical ingredient for the development of new drugs. Its unique molecular structure and properties may contribute to the treatment of various diseases and conditions, although further research is needed to determine its specific therapeutic applications and efficacy.
Used in Agricultural Products:
5-OXO-2,3-DIHYDRO-5H-PYRIMIDO[2,1-B][1,3]THIAZOLE-6-CARBOXYLIC ACID may be utilized as a component in agricultural products, such as pesticides or fertilizers, due to its unique chemical properties. Its potential applications in this industry could contribute to the development of more effective and environmentally friendly solutions for crop protection and enhancement.
Used in Other Industrial Processes:
5-OXO-2,3-DIHYDRO-5H-PYRIMIDO[2,1-B][1,3]THIAZOLE-6-CARBOXYLIC ACID's unique structure and properties may also find applications in other industrial processes, such as the synthesis of specialty chemicals, materials science, or as intermediates in the production of other complex organic compounds. Further research and analysis are necessary to explore the specific uses and potential benefits of 5-OXO-2,3-DIHYDRO-5H-PYRIMIDO[2,1-B][1,3]THIAZOLE-6-CARBOXYLIC ACID in these industries.

Check Digit Verification of cas no

The CAS Registry Mumber 32084-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,0,8 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 32084-55:
(7*3)+(6*2)+(5*0)+(4*8)+(3*4)+(2*5)+(1*5)=92
92 % 10 = 2
So 32084-55-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O3S/c10-5-4(6(11)12)3-8-7-9(5)1-2-13-7/h3H,1-2H2,(H,11,12)/p-1

32084-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-oxo-2,3-dihydro-[1,3]thiazolo[3,2-a]pyrimidine-6-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-Oxo-2,3-dihydro-5H-pyrimido[2,1-b][1,3]thiazole-6-carboxylic acid

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:32084-55-2 SDS

32084-55-2Relevant articles and documents

Synthesis & Biological Activity of Some New Carboxamides, Carbohydrazides & Carbamates Derived from 2,3-Dihydro-5(H)-oxothiazolopyrimidine-6-carboxylic Acid

Shridhar, D. R.,Jogibhukta, M.,Joshi, P. P.,Rao, C. Seshagiri,Junnarkar, A. Y.

, p. 492 - 494 (2007/10/02)

Some new carboxamides (Va-j), carbohydrazides (Vk-p) and carbamates (VIIIa-d) derived from 2,3-dihydro-5(H)-oxothiazolopyrimidine-6-carboxylic acid (III) have been synthesised and evaluated for their antiinflammatory, antibacterial, antifungal and anthelmintic activities.The carboxamides (Ve,i,j) and carbohydrazides (Vk,n,o) possess promising antiinflammatory activity against carrageenin-induced paw oedema in rats, compound Ve being the most active member of the series showing 50.8 percent inhibition at 200 mg/kg (p.o.) dose.Ve, however, is found to be inactive at lower doses.None of the compounds shows any noteworthy antibacterial, antifungal or anthelmintic activities except Vk which displays promising antitubercular activity in vitro (MIC=5 mcg/ml) against Mycobacterium tuberculosis H37Rv.

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