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112006-75-4

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112006-75-4 Usage

Description

3-Pyridinecarboxamide,2-(aminosulfonyl)-N,N-dimethyl-, also known as N,N-Dimethylnicotinamide-2-sulfonamide (CAS# 112006-75-4), is a light yellow powder compound with significant utility in the field of organic synthesis. Its unique chemical structure and properties make it a valuable component for various applications across different industries.

Uses

Used in Organic Synthesis:
3-Pyridinecarboxamide,2-(aminosulfonyl)-N,N-dimethylis used as a key intermediate in the synthesis of various organic compounds. Its versatile chemical properties allow it to be employed in the creation of a wide range of products, from pharmaceuticals to agrochemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Pyridinecarboxamide,2-(aminosulfonyl)-N,N-dimethylis used as a building block for the development of new drugs. Its unique structure and reactivity make it a promising candidate for the synthesis of novel therapeutic agents with potential applications in treating various diseases and medical conditions.
Used in Agrochemical Industry:
3-Pyridinecarboxamide,2-(aminosulfonyl)-N,N-dimethylis also utilized in the agrochemical industry for the synthesis of new pesticides and other crop protection agents. Its chemical properties enable the development of innovative products that can help improve crop yield and protect plants from various pests and diseases.
Used in Dye and Pigment Industry:
In the dye and pigment industry, 3-Pyridinecarboxamide,2-(aminosulfonyl)-N,N-dimethylis used as a starting material for the production of various dyes and pigments. Its light yellow color and chemical properties make it suitable for the development of new colorants with improved performance and stability.
Used in Research and Development:
3-Pyridinecarboxamide,2-(aminosulfonyl)-N,N-dimethylis also used in research and development laboratories for the exploration of new chemical reactions and the synthesis of novel compounds. Its unique properties make it an interesting subject for scientific investigation and the potential discovery of new applications and uses.

Check Digit Verification of cas no

The CAS Registry Mumber 112006-75-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,0,0 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 112006-75:
(8*1)+(7*1)+(6*2)+(5*0)+(4*0)+(3*6)+(2*7)+(1*5)=64
64 % 10 = 4
So 112006-75-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H11N3O3S/c1-11(2)8(12)6-4-3-5-10-7(6)15(9,13)14/h3-5H,1-2H3,(H2,9,13,14)

112006-75-4SDS

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 2-Aminosulfonyl-N,N-Dimethylnicotinamide

1.2 Other means of identification

Product number -
Other names N,N-Dimethyl-2-sulfamoylnicotinamide

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:112006-75-4 SDS

112006-75-4Relevant articles and documents

Preparation method of 2-aminosulfonyl-N, N-dimethyl nicotinamide

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, (2021/05/19)

The invention provides a preparation method of 2-aminosulfonyl-N, N-dimethyl nicotinamide. The preparation method comprises the following steps: synthesizing 2-chlorine-N, N-dimethyl nicotinamide by taking 2-cyano-5-dimethylamino-2, 4-pentadienyl dicarboxamide and hydrochloric acid gas as raw materials, and reacting at the temperature of between 0 and 100 DEG C to synthesize the 2-chloro-N, N-dimethyl nicotinamide. Furthermore, the preparation method provided by the invention also comprises the step of sequentially synthesizing the 2-sulfydryl-N, N-dimethyl nicotinamide, the 2-chlorosulfonyl-N, N-dimethyl nicotinamide and the 2-aminosulfonyl-N, N-dimethyl nicotinamide by taking the 2-chloro-N, N-dimethyl nicotinamide as a raw material. According to the preparation method of the 2-aminosulfonyl-N, N-dimethyl nicotinamide, provided by the invention, the novel preparation method is provided by taking the 2-cyano-5-dimethylamino-2, 4-pentadiene dicarboxamide as an initial raw material, and the preparation method is relatively short in synthetic route, relatively high in yield and relatively low in cost.

Preparation method of nicosulfamide

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, (2021/03/13)

The invention relates to the technical field of pesticide synthesis, in particular to a preparation method of nicosulfamide. The preparation method of the smoke sulfonamide comprises the following steps: taking 3-cyanopyridine as a raw material, and carrying out oxidation reaction to obtain 3-cyanopyridine nitric oxide; carrying out sulfonation reaction and ammoniation reaction on the 3-cyanopyridine nitrogen oxide to obtain 2-sulfonamido-3-cyanopyridine; carrying out alkaline hydrolysis on the 2-sulfamido-3-cyanopyridine to obtain 2-sulfamido nicotinic acid; and carrying out amidation reaction on the nicotinic acid 2-sulfonamide to obtain the nicotinamide. The preparation method of the nicosulfamide is simple to operate and low in raw material cost, by-products generated in the preparation process can be recycled, the cost is saved, and the prepared nicosulfamide is high in yield and purity.

Synthesis method of 2-aminosulfonyl-N, N-dimethyl nicotinamide

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Paragraph 0015-0021, (2020/11/26)

The invention belongs to the field of pesticides, relates to a synthesis technology of a nicosulfuron intermediate, in particular to a synthesis method of 2-aminosulfonyl-N, N-dimethyl nicotinamide. According to the method, 2-chloro-N, N-dimethyl nicotinamide and sodium thiosulfate are used as raw materials, the method comprises the processes of sulfhydrylation, sulfonation, ammoniation reaction and the like, the reaction process is few in by-product, high in yield and low in raw material cost, hydrogen sulfide is removed from the source of the reaction, real clean production is achieved, andthe product content and yield are increased.

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