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2825-15-2

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2825-15-2 Usage

General Description

1-nitroimidazolidine-2,4-dione is a chemical compound with the molecular formula C3H4N4O3. It is a nitroimidazole derivative that has been used as a building block in the synthesis of various pharmaceuticals and biologically active compounds. 1-nitroimidazolidine-2,4-dione possesses a nitro group, which imparts it with potential biological activity, particularly as an anti-infective agent. Its structure and properties make it a valuable intermediate in organic synthesis, as it can be used to create a wide range of functionalized derivatives with various applications. Additionally, 1-nitroimidazolidine-2,4-dione has the potential to be used as a precursor in the development of novel drugs and therapeutic agents due to its unique chemical and biological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 2825-15-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,2 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2825-15:
(6*2)+(5*8)+(4*2)+(3*5)+(2*1)+(1*5)=82
82 % 10 = 2
So 2825-15-2 is a valid CAS Registry Number.

2825-15-2SDS

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 1-nitrohydantoin

1.2 Other means of identification

Product number -
Other names 1-nitro-imidazolidine-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:2825-15-2 SDS

2825-15-2Upstream product

2825-15-2Downstream Products

2825-15-2Relevant articles and documents

Gas/Solid Reactions with Nitrogen Dioxide

Kaupp, Gerd,Schmeyers, Jens

, p. 5494 - 5503 (2007/10/02)

Numerous gas/solid reactions of nitrogen dioxide with organic substrates are investigated preparatively and mechanistically.Gaseous NO2 reacts with crystalline stable free radicals (nitroxyls 1, verdazyl 6) by electron transfer.The nitrite ions formed are irreversibly oxidized by NO2 via oxygen atom transfer.Solid cation nitrates are formed quantitatively.Thione bonds of thiohydantoins 8 are transformed to carbonyl bonds with formation of sulfur and NO presumably via nitrites as intermediates.Hydantoin 13 oxygenates at its free 5-methylene group via C-H abstraction and nitrite or it undergoes N-1 nitration via N-H abstraction depending on the conditions.Both reactions proceed quantitatively. 1,3-Oxazolidin-2-one (15) gives N-nitration and N-nitrosation with the NO produced.Nonenolized crystalline barbituric acids 17 are quantitatively nitrated (C-N bond formation with radicals) at their methylene groups. 4-Hydroxybenzaldehyde (19) and vanilline (22) give quantitative aromatic nitration (C-N bond formation with arenes) without melting.All possible regioisomers are formed.Solid 9-methylanthracene (26) gives a quantitative yield of its 10-nitro derivative 27.Crystalline anthracene (28) and gaseous NO2 yield 3 primary products 29 (cis; trans) and the new dimeric product 30 as well as the stable secondary products 31 and 32.The gas/solid tetranitration of tetraphenylethylene (33) is severely hindered by the water of reaction.However, a 95percent yield of pure tetrakis(p-nitrophenyl)ethylene is obtained if the drying agent MgSO4*2H2O is admixed and the product 34 extracted.The gas/solid procedures avoid solvents and fuming nitric acid.They give pure products without necessity for recrystallization in most cases and they avoid wastes.Atomic force microscopy (AFM) measurements on prominent faces of single crystals of 1a, 11a, 28, and 33 reveal phase rebuildings with well-directed long-range molecular transport.Nanoliquids were only present on (110) of 28.The characteristic AFM features are correlated with known X-ray crystal structure data and compared with previous results.The shape of the features depends on the molecular packing in the crystal bulk and on the molecular shapes.Molecular interpretations of the AFM features are given.

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