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N,2-Dicyanoacetamide sodium salt is a versatile chemical compound characterized by the presence of both cyano and amide functional groups. It is recognized for its solubility in water due to its sodium salt form, which facilitates its use in aqueous reactions. N,2-DICYANOACETAMIDE SODIUM SALT is valued for its capacity to participate in a range of chemical transformations, such as nucleophilic substitution, metal complexation, and condensation reactions. Its applications extend beyond traditional organic synthesis, with roles in the development of new materials and the preparation of organic electronic devices.

1189-10-2

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1189-10-2 Usage

Uses

Used in Organic Synthesis:
N,2-Dicyanoacetamide sodium salt is utilized as a reagent in organic synthesis for its ability to engage in various chemical reactions, contributing to the formation of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, N,2-Dicyanoacetamide sodium salt serves as an intermediate, playing a crucial role in the synthesis of various drugs, thereby aiding in the development of new medicinal compounds.
Used in Agrochemical Production:
Similarly, in agrochemicals, this sodium salt is employed as an intermediate, facilitating the synthesis of compounds that are vital for agricultural applications, such as pesticides and herbicides.
Used in Material Development:
N,2-Dicyanoacetamide sodium salt is also used in the development of innovative materials, potentially leading to advancements in various industrial sectors.
Used in Organic Electronic Devices:
Furthermore, N,2-DICYANOACETAMIDE SODIUM SALT finds application in the preparation of organic electronic devices, where its unique properties can be harnessed to improve device performance or enable new functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 1189-10-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,8 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1189-10:
(6*1)+(5*1)+(4*8)+(3*9)+(2*1)+(1*0)=72
72 % 10 = 2
So 1189-10-2 is a valid CAS Registry Number.
InChI:InChI=1/C4HN3O3.Na/c5-1-7-3(8)4(9)10-2-6;/h(H,7,8);/q;+1/p-1

1189-10-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,(2-cyanato-2-oxoacetyl)-cyanoazanide

1.2 Other means of identification

Product number -
Other names sodium N,2-dicyanoacetamidate,monosodium salt

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:1189-10-2 SDS

1189-10-2Downstream Products

1189-10-2Relevant academic research and scientific papers

General synthesis of 1-Aryl-6-azaisocytosines and their utilization for the preparation of related condensed 1,2,4-Triazines

Slouka, Jan,Styskala, Jakub,Zále?ák, Franti?ek

, (2019)

A simple general synthesis of 1-aryl-6-azaisocytosine-5-carbonitriles 4 is described. This method is based on coupling diazonium salts with cyanoacetylcyanamide 2 and then cyclization of the formed 2-arylhydrazono-2-cyanoacetylcyanamides 3. The 6-azaisocytosines 4 were studied with respect to tautomeric equilibrium and the transformation of functional groups, and used in the synthesis of the condensed heterocyclic compounds: Purine isosteric imidazo[2,1-c]-[1,2,4]triazine 8 and the 1,2,4-triazino[2,3-a]quinazolines 9-12.

MODULATORS OF TOLL-LIKE RECEPTORS

-

Page/Page column 68, (2010/06/19)

Provided are modulators of TLRs of Formula II: pharmaceutically acceptable salts thereof, compositions containing such compounds, and therapeutic methods that include the administration of such compounds.

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