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5-bromo-1-(tetrahydro-2H-pyran-2-yl)pyrimidine-2,4(1H,3H)-dione is a complex organic compound with the molecular formula C9H12BrN2O3. It is a derivative of pyrimidine, a heterocyclic aromatic organic compound consisting of a six-membered ring, with four carbon atoms and two nitrogen atoms. In this specific compound, the pyrimidine ring is substituted with a bromine atom at the 5th position and a tetrahydro-2H-pyran-2-yl group at the 1st position. The compound also features two carbonyl groups at the 2nd and 4th positions, which are part of the 1H,3H-dione structure. This chemical is known for its potential applications in medicinal chemistry, particularly in the synthesis of various biologically active compounds. Its unique structure allows it to form part of larger molecules with specific therapeutic properties, making it a valuable intermediate in the development of new drugs.

5580-89-2

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5580-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5580-89-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,8 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5580-89:
(6*5)+(5*5)+(4*8)+(3*0)+(2*8)+(1*9)=112
112 % 10 = 2
So 5580-89-2 is a valid CAS Registry Number.

5580-89-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-1-(oxan-2-yl)pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-bromo-1-tetrahydropyran-2-yl-1H-pyrimidine-2,4-dione

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:5580-89-2 SDS

5580-89-2Upstream product

5580-89-2Downstream Products

5580-89-2Relevant academic research and scientific papers

The bromination and iodination of N1-substituted uracils

Bakker, Cees N. M.,Kaspersen, Frans M.

, p. 267 - 271 (2007/10/02)

Reaction of N1-substituted uracils with bromine in water at pH=7 leads to 5-bromo-6-hydroxy-5,6-hydrouracils.For different N1-substituents these products were isolated and the relatively stable derivatives were characterized by 1H NMR and mass spectroscopy.On electrophilic iodination with iodide and chloramine-T in water no indications were obtained for the formation of such dihydrouracils except for uridine and deoxyuridine.However, on reaction of N1-substituted uracils with N-iodosuccinimide in CHCl3 containing ethanol, or in ethanol, 5-iodo-6-ethoxy-5,6-dihydrouracils could be isolated as reaction products.

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