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125815-68-1

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125815-68-1 Usage

Description

2-Amino-4-cyano-5-imidazolecarboxamide is a synthetic intermediate that is characterized as a crystalline solid. It is a chemical compound with a unique structure that consists of an imidazole ring, an amide group, and a cyano group attached to different positions on the ring. 2-AMINO-4-CYANO-5-IMIDAZOLECARBOXAMIDE is known for its potential applications in various industries due to its chemical properties.

Uses

Used in Pharmaceutical Industry:
2-Amino-4-cyano-5-imidazolecarboxamide is used as a synthetic intermediate for the development of pharmaceutical compounds. Its unique structure allows it to be a key component in the synthesis of various drugs, particularly those targeting specific biological pathways or receptors.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Amino-4-cyano-5-imidazolecarboxamide is used as a building block for the synthesis of various agrochemicals, such as pesticides and herbicides. Its ability to form stable compounds with other molecules makes it a valuable intermediate in the development of effective and targeted agrochemical products.
Used in Material Science:
2-Amino-4-cyano-5-imidazolecarboxamide is also used in material science for the development of new materials with specific properties. Its ability to form stable complexes with other molecules can be utilized to create materials with unique characteristics, such as improved stability, enhanced reactivity, or specific binding properties.
Used in Research and Development:
As a synthetic intermediate, 2-Amino-4-cyano-5-imidazolecarboxamide is widely used in research and development for the exploration of new chemical reactions and the synthesis of novel compounds. Its unique structure and properties make it an interesting candidate for studying various chemical and biological phenomena.

Check Digit Verification of cas no

The CAS Registry Mumber 125815-68-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,8,1 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 125815-68:
(8*1)+(7*2)+(6*5)+(5*8)+(4*1)+(3*5)+(2*6)+(1*8)=131
131 % 10 = 1
So 125815-68-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H5N5O/c6-1-2-3(4(7)11)10-5(8)9-2/h(H2,7,11)(H3,8,9,10)

125815-68-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-4-cyano-1H-imidazole-5-carboxamide

1.2 Other means of identification

Product number -
Other names 1H-Imidazole-5-carboxamide,2-amino-4-cyano

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:125815-68-1 SDS

125815-68-1Downstream Products

125815-68-1Relevant articles and documents

Synthesis of nitrogen-rich imidazole, 1,2,4-triazole and tetrazole-based compounds

Srinivas, Dharavath,Ghule, Vikas D.,Muralidharan, Krishnamurthi

, p. 7041 - 7051 (2014)

Imidazole, 1,2,4-triazole and tetrazole based molecules were prepared for their possible applications in nitrogen-rich gas generators. The energetic salts of 1-(1H-1,2,4-triazol-3-yl)-1H-tetrazole (9), 5-(1H-tetrazol-1-yl)-1H-1,2,4- triazol-3-amine (10), 1-(3-azido-1H-1,2,4-triazol-5-yl)-1H-tetrazole (11) and 3-azido-1H-1,2,4-triazol-5-amine (12) were prepared with various cationic moieties. Their densities, heats of formation, chemical energy of detonation, detonation velocities and pressures were calculated. All of the compounds possessed high positive heats of formation due to high energy contribution from the molecular backbone of the corresponding compounds. The effect of the azole rings and nitro, amino, and azido groups on their physicochemical properties was examined and discussed. The Royal Society of Chemistry 2014.

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