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1189-10-2

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1189-10-2 Usage

General Description

N,2-Dicyanoacetamide sodium salt is a chemical compound containing both cyano and amide functional groups. It is commonly used as a reagent in organic synthesis and as an intermediate in the production of pharmaceuticals and agrochemicals. Its sodium salt form makes it more soluble in water, allowing for easier handling and use in aqueous reactions. N,2-DICYANOACETAMIDE SODIUM SALT is known for its ability to undergo various chemical transformations, including nucleophilic substitution reactions, metal complexation, and condensation reactions. N,2-Dicyanoacetamide sodium salt is also used in the development of new materials and in the preparation of organic electronic devices.

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 articles and documents

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.

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