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1752-96-1

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1752-96-1 Usage

Description

NICOTINANILIDE, also known as Nicotinic Anilide, is a compound with the CAS number 1752-96-1. It is a yellow crystalline solid that is useful in organic synthesis. Its chemical properties make it a valuable component in various applications across different industries.

Uses

Used in Organic Synthesis:
NICOTINANILIDE is used as a synthetic compound for its utility in organic synthesis processes. Its unique chemical properties allow it to be a valuable building block in the creation of more complex molecules and compounds.
Used in Pharmaceutical Industry:
NICOTINANILIDE is used as an intermediate in the pharmaceutical industry for the development of new drugs. Its role in organic synthesis makes it a key component in the production of various medications.
Used in Chemical Research:
NICOTINANILIDE is used as a research compound for studying its properties and potential applications in chemical reactions. This helps scientists and researchers to better understand its behavior and how it can be utilized in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 1752-96-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,5 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1752-96:
(6*1)+(5*7)+(4*5)+(3*2)+(2*9)+(1*6)=91
91 % 10 = 1
So 1752-96-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H10N2O/c15-12(10-5-4-8-13-9-10)14-11-6-2-1-3-7-11/h1-9H,(H,14,15)

1752-96-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Detail
  • Alfa Aesar

  • (L06154)  Nicotinanilide, 98%   

  • 1752-96-1

  • 5g

  • 529.0CNY

  • Detail
  • Alfa Aesar

  • (L06154)  Nicotinanilide, 98%   

  • 1752-96-1

  • 25g

  • 1682.0CNY

  • Detail
  • Aldrich

  • (454826)  Nicotinanilide  97%

  • 1752-96-1

  • 454826-5G

  • 478.53CNY

  • Detail

1752-96-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenylpyridine-3-carboxamide

1.2 Other means of identification

Product number -
Other names 3-Pyridinecarboxamide,N-phenyl

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:1752-96-1 SDS

1752-96-1Relevant articles and documents

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Rohrlich

, p. 119,123 (1955)

-

Direct Synthesis of N,N-Disubstituted Formamides by Oxidation of Imines Using an HFIP/UHP System

Llopis, Natalia,Gisbert, Patricia,Baeza, Alejandro

, p. 11072 - 11079 (2020)

The straightforward synthesis of N,N-disubstituted formamides using a combination of 1,1,1,3,3,3-hexafluoroispropanol (HFIP) and H2O2 is described. The unique features of HFIP allowed the utilization of a green oxidant such as H2O2, and the products, arising from an oxidation-rearrangement sequence, were obtained in good to high yields under smooth reaction conditions.

Method for preparing amide compound by photocatalysis of organic amine

-

Paragraph 0044-0045, (2021/06/06)

The invention relates to the technical field of organic synthesis, in particular to a method for preparing amide compounds through photocatalysis of organic amine. The preparation method comprises the following steps: mixing tetrahalomethane with a solvent, sequentially adding an amine compound, a catalyst and organic carboxylic acid, performing stirring and reacting under an oxygen-containing atmosphere and an illumination condition, and performing separating and purifying to obtain the amide compound with a structure shown in formulas V-VII. According to the method, the reaction is carried out in the air atmosphere under the illumination condition at room temperature and normal pressure, the reaction condition is mild, the raw material source is wide, the cost is low, the byproduct generated after the reaction is the halogen simple substance, the added value is high, a large amount of waste is avoided, and the method has higher atom economy and environmental friendliness and is beneficial to large-scale production.

Activated charcoal supported copper nanoparticles: A readily available and inexpensive heterogeneous catalyst for the N-arylation of primary amides and lactams with aryl iodides

Zhao, Rong,Dong, Wenwen,Teng, Jiangge,Wang, Zhiwei,Wang, Yunzhong,Yang, Jianguo,Jia, Qiang,Chu, Changhu

supporting information, (2020/12/21)

A novel heterogeneous copper catalyst has been developed by supporting copper nanoparticles on activated charcoal via in situ reducing copper(II) with aqueous hydrazine as reductant. The characterization of Cu/C catalyst showed that the Cu0 nano-particles were formed on the surface of charcoal. This catalyst displayed good catalytic activities toward the N-arylation of primary amides and lactams with aryl iodides.

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