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3-Nitro-4,5-dihydro-1,2-oxazole 2-oxide is a complex organic compound with the chemical formula C3H4N2O5. It is a derivative of the 1,2-oxazole ring system, which is a five-membered heterocyclic compound containing one oxygen and two nitrogen atoms. The molecule features a nitro group (-NO2) at the 3-position and a hydroxyl group (-OH) at the 2-position, which is further oxidized to a hydroperoxide (-OOH). 3-nitro-4,5-dihydro-1,2-oxazole 2-oxide is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals. Due to its reactive functional groups, it is important to handle 3-nitro-4,5-dihydro-1,2-oxazole 2-oxide with care, as it may be sensitive to heat, light, and other reactive conditions.

4122-45-6

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4122-45-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4122-45-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,2 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4122-45:
(6*4)+(5*1)+(4*2)+(3*2)+(2*4)+(1*5)=56
56 % 10 = 6
So 4122-45-6 is a valid CAS Registry Number.

4122-45-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-nitro-2-oxido-4,5-dihydro-1,2-oxazol-2-ium

1.2 Other means of identification

Product number -
Other names 3-nitro-4,5-dihydro-isoxazole 2-oxide

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:4122-45-6 SDS

4122-45-6Relevant academic research and scientific papers

The structural aspects of the transformation of 3-nitroisoxazoline-2-oxide to 1-aza-2,8-dioxabicyclo[3.3.0]octane derivatives: Experimental and MEDT theoretical study

Woliński, Przemys?aw,K?cka-Zych, Agnieszka,Dziuk, B?a?ej,Ejsmont, Krzysztof,?apczuk-Krygier, Agnieszka,Dresler, Ewa

, p. 27 - 34 (2019)

Reaction of 3-nitroisoxazoline-2-oxide with monosubstituted ethenes, first time documented fifty years ago, have been reviewed. Structures of phenyl and cyano derivatives of 1-aza-2,8-dioxabicyclo[3.3.0]octane produced in [3 + 2]cycloaddition (32CA)betwee

The first synthesis of 1,1-dinitrocyclopropane

Budynina, Ekaterina M.,Averina, Elena B.,Ivanova, Olga A.,Yashin, Nikolai V.,Kuznetsova, Tamara S.,Zefirov, Nikolai S.

, p. 2609 - 2610 (2007/10/03)

1,1-Dinitrocyclopropane was prepared in 62% yield. This high energetic compound was previously unknown. Herein its preparation via tandem reaction between nitroform and diazomethane in benzene is described.

Synthesis of Alkyl Nitronates via Mitsunobu Condensation

Falck, J. R.,Yu, Jurong

, p. 6723 - 6726 (2007/10/02)

Nitroalkanes bearing electron-withdrawing or unsaturated substituents at the α-carbon experience exclusive intra- and intermolecular O-alkylation by alcohols under Mitsunobu condensation conditions furnishing good to excellent yields of alkyl nitronates;

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