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1,2,4-Oxadiazol-5-amine, 3-(4-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23275-46-9

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23275-46-9 Usage

Appearance

White to light yellow crystalline powder

Usage

Often used in the synthesis of other organic compounds

Application

Commonly employed in pharmaceutical research and development

Pharmacological properties

Potential pharmacological properties

Handling

Important to handle with care

Health and environmental risks

May pose health and environmental risks if not properly managed

Check Digit Verification of cas no

The CAS Registry Mumber 23275-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,7 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 23275-46:
(7*2)+(6*3)+(5*2)+(4*7)+(3*5)+(2*4)+(1*6)=99
99 % 10 = 9
So 23275-46-9 is a valid CAS Registry Number.

23275-46-9Downstream Products

23275-46-9Relevant academic research and scientific papers

SYNTHESES WITH NITRILE OXIDES. 2. REACTION OF AROMATIC NITRILE OXIDES WITH BIS(TRIMETHYLSILYLCARBODIIMIDE)

Ogurtsov, V. A.,Rakitin, O. A.,Obruchnikova, N. V.,Khmel'nitskii, L. I.

, p. 1910 - 1912 (2007/10/02)

The reaction of aromatic nitrile oxides with bis(trimethylsilylcarbodiimide) gives 5-amino-3-aryl-1,2,4-oxadiazoles.Keywords: nitrile oxides, oxadiazoles, carbodiimide.

SYNTHESIS AND THERMOLYSIS OF SOME N-HYDROXIMOYL- AND N-HYDRAZONOYLAZOLES

Plenkiewicz, Jan,Zdrojewski, Tadeusz

, p. 675 - 710 (2007/10/02)

The reactions of nitrile oxides or nitrile imines with pyrazole, imidazole, 1,2,3- and 1,2,4-triazole or tetrazole derivatives yield the appropriate N-hydroximoyl- or N-hydrazonoylazoles.Thermolysis of 1-hydroximoyltetrazoles, depending on the nature of the substituents in the tetrazole ring, yields 1,2,4-oxadiazoles or 5-amino-1,2,4-oxadiazoles upon hydrazoic acid or nitrogen evolution.Under similar conditions, 1-hydrazonoyltetrazoles give 1,2,4-triazoles or 5-amino-1,2,4-triazoles while 2-hydrazonoyltetrazoles decompose to the dihydro-1,2,4,5-tetrazine derivatives.

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