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Acetamide, N-(4-nitro-2-pyridinyl)-, oxide (9CI) is a chemical compound with the molecular formula C7H7N2O3. It is an organic compound derived from acetamide, where a 4-nitro-2-pyridinyl group is attached to the nitrogen atom. The oxide part of the name indicates the presence of an oxygen atom in the molecule. Acetamide, N-(4-nitro-2-pyridinyl)-, oxide (9CI) is primarily used in research and development, particularly in the synthesis of various pharmaceuticals and agrochemicals. It is an important intermediate in the preparation of certain drugs and can also be used as a reagent in chemical reactions. Due to its potential applications in the pharmaceutical industry, it is essential to understand its properties and reactivity to develop new and effective compounds.

4487-48-3

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4487-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4487-48-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,8 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4487-48:
(6*4)+(5*4)+(4*8)+(3*7)+(2*4)+(1*8)=113
113 % 10 = 3
So 4487-48-3 is a valid CAS Registry Number.

4487-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-nitro-1-oxy-pyridin-2-yl)-acetamide

1.2 Other means of identification

Product number -
Other names -

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:4487-48-3 SDS

4487-48-3Relevant academic research and scientific papers

Synthesis method of 2-amino-4-fluoropyridine

-

, (2018/03/23)

The invention discloses a synthesis method of 2-amino-4-fluoropyridine. The synthesis method comprises the following synthesis steps: 1, taking diaminopyridine as the raw material, carrying out oxidation reaction to prepare 2-aminopyridine N-oxide a; 2, subjecting the compound a to nitration reaction with mixed acid to obtain 2-amino-4-nitropyridine N-oxide b; 3, carrying out acylation reaction onthe compound b and an acylation reagent to obtain 2-acetamino-4-nitropyridine N-oxide c; 4, carrying out reduction reaction on the compound c to obtain 2-acetamino-4-aminopyridine d; 5, carrying outdiazo-reaction on the compound d and HBF4 to obtain diazonium fluoroborate e; and 6, carrying out Balz-Schiemann reaction on the compound e to introduce fluorine atoms and conducting hydrolysis deacetylation to obtain 2-amino 4-fluoropyridine. The method provided by the invention solves the problems of long synthesis route, complicated operation, serious pollution, high cost, low yield and the like in existing synthesis methods.

Structural and vibrational investigation of 2-amino-4-nitropyridine crystal

Oszust,Talik,Pietraszko,Marchewka,Baran

, p. 53 - 63 (2007/10/03)

The X-ray structure of 2-amino-4-nitropyridine was determined at room temperature. The crystal belongs to the P2(I)/c space group of the monoclinic system (Z = 4, a = 6.7290(10), b = 10.946(2), c = 9.060(2) A, β = 100.03(3) deg) and is built of layers parallel to the (102) crystallographic plane. The molecules in the layer are joined into centrosymmetric dimers by two N-H···N hydrogen bonds (N···N distance = 3.011(3) A), which form rings of C(i) symmetry. The other N-H bonds of the amino groups are involved in N-H···O hydrogen bonds with the oxygen atoms of the nitro groups (N···O distance = 3.054(3) A). These hydrogen bonds join the dimers into an infinite plane. The powder IR and Raman spectra (4000-80 cm-1) were measured for normal and deuterated crystals and are discussed with respect to the crystal structure. The N-H stretching vibrations behave as the stretching vibrations of two almost independent hydrogen bonds. Strong A(g)-A(u)-type splitting is observed for the stretching vibrations of the N-H···N type hydrogen bonds.

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