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1,2,4-Oxadiazole-3-carboximidoylchloride,N-hydroxy-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128452-48-2

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128452-48-2 Usage

Derivative of

1,2,4-oxadiazole

Primary use

Synthesis of pharmaceuticals and other organic compounds

Potential as a reagent

Formation of carbon-nitrogen and carbon-oxygen bonds in various organic reactions

Biological activity

Exhibits biological activity, valuable in medicinal chemistry research

Safety precautions

Proper handling and safety measures should be taken to minimize risk of exposure and ensure safe laboratory practices

Check Digit Verification of cas no

The CAS Registry Mumber 128452-48-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,4,5 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 128452-48:
(8*1)+(7*2)+(6*8)+(5*4)+(4*5)+(3*2)+(2*4)+(1*8)=132
132 % 10 = 2
So 128452-48-2 is a valid CAS Registry Number.

128452-48-2SDS

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 3-[chloro(nitroso)methylidene]-1,2,4-oxadiazole

1.2 Other means of identification

Product number -
Other names 1,2,4-oxadiazol-3-carbohydroximoyl chloride

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:128452-48-2 SDS

128452-48-2Relevant academic research and scientific papers

Synthesis and Characterization of the Potential Melt-Castable Explosive 3-(1,2,4-Oxadiazolyl)-5-Nitratomethyl Isoxazole

Byrd, Edward F. C.,Johnson, Eric C.,Miller, Christopher W.,Orlicki, Joshua A.,Reid, Tristen A.,Sabatini, Jesse J.,Sausa, Rosario C.

, p. 875 - 878 (2021/07/22)

The synthesis of 3-(1,2,4-oxadiazolyl)-5-nitratomethyl isoxazole (C6H4N4O5), its physical properties, and its theoretical performances are described. This energetic material was found to have a melting point range of 76.6–79.2 °C, and a thermal onset decomposition temperature of 184.5 °C. These thermal features put this material into the standalone melt-castable explosive class. The material was found to have TNT performance, and was found to be insensitive to impact, friction, and electrostatic discharge, despite having a nitric ester functionality. A critical reaction in making this molecule was the desymmetrization of diaminoglyoxime. The optimization of this transformation is described. Previous reports of this desymmetrization were found to be inaccurate, as the desymmetrization reaction produces a co-crystal of mono- and bi-1,2,4-oxadiazole products.

Exploiting the energetic potential of 1,2,4-oxadiazole derivatives: Combining the benefits of a 1,2,4-oxadiazole framework with various energetic functionalities

Yan, Chao,Wang, Kangcai,Liu, Tianlin,Yang, Hongwei,Cheng, Guangbin,Zhang, Qinghua

, p. 14210 - 14218 (2017/11/06)

A series of 1,2,4-oxadiazole-derived energetic compounds were successfully synthesized using 1,2,4-oxadiazole-3-chloroxime as a versatile starting material. These energetic compounds were fully characterized by NMR spectroscopy, IR spectroscopy, and elemental analysis. The structures of compounds 5, 6a, 6c, 8 and 8a were determined by single crystal X-ray diffraction. The physicochemical and energetic properties of all the synthesized energetic compounds, including density, thermal stability and energetic performance (e.g., detonation velocities and detonation pressures) were investigated. Among these energetic compounds, hydrazinium salts 6b and 8b and hydroxylammonium salts 6c and 8c exhibit satisfactory calculated detonation performances, which outperform the commonly used high explosive RDX. Potassium salt 5 shows good detonation performance, high density as well as high sensitivity, making it a potential primary explosive. Compound 9 is a potential candidate for melt-cast explosives due to its remarkable liquid range between melting point (Tm = 98 °C) and decomposition temperature (Td = 208 °C).

SYNTHESIS OF THE AMIDES AND ACID HALIDES OF 1,2,4-OXADIAZOLE-3-CARBOHYDROXAMIC ACID

Andrianov, V. G.,Semenikhina, V. G.,Eremeev, A. V.

, p. 475 - 477 (2007/10/02)

The reaction of diaminoglyoxime with carboxylic acid derivatives gave the amidoximes of 1,2,4-oxadiazole-3-carboxylic acid.It has been found that in the nitrozation of the obtained amidoximes in a solution of hydrochloric or hydrobromic acid the corresponding halooximes are formed.

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