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1-(2-hydroxy-3-nonyl)imidazole-4-carboxamide is a chemical compound that belongs to the class of imidazoles, which are organic compounds containing an imidazole ring. It is characterized by a hydroxy group attached to the second position and a nonyl group attached to the third position of the imidazole ring, with a carboxamide group at the fourth position. 1-(2-hydroxy-3-nonyl)imidazole-4-carboxamide is known for its potential applications in the synthesis of pharmaceuticals and as a building block in organic chemistry, as well as its possible use in developing new materials and bioactive compounds. The specific properties and potential uses of 1-(2-hydroxy-3-nonyl)imidazole-4-carboxamide may vary depending on its purity and the conditions of its synthesis.
Usage:
Used in Pharmaceutical Synthesis:
1-(2-hydroxy-3-nonyl)imidazole-4-carboxamide is used as an intermediate for the synthesis of various pharmaceuticals, due to its unique chemical structure and reactivity. Its presence in the synthesis process can contribute to the development of new drugs with improved efficacy and reduced side effects.
Used in Organic Chemistry:
As a building block in organic chemistry, 1-(2-hydroxy-3-nonyl)imidazole-4-carboxamide is used for the creation of more complex organic molecules. Its versatile structure allows for further functionalization and modification, leading to a wide range of potential applications in the field of chemistry.
Used in Material Science:
1-(2-hydroxy-3-nonyl)imidazole-4-carboxamide may have potential applications in the development of new materials, thanks to its unique chemical properties. It could be used to create novel materials with specific characteristics, such as improved mechanical strength, thermal stability, or chemical resistance.
Used in Bioactive Compound Development:
1-(2-hydroxy-3-nonyl)imidazole-4-carboxamide may also be utilized in the development of bioactive compounds, which are molecules that can interact with biological systems to produce a desired effect. Its unique structure and properties could make it a valuable component in the design and synthesis of new bioactive molecules with potential applications in medicine, agriculture, and other industries.

130573-54-5

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130573-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130573-54-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,5,7 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 130573-54:
(8*1)+(7*3)+(6*0)+(5*5)+(4*7)+(3*3)+(2*5)+(1*4)=105
105 % 10 = 5
So 130573-54-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H23N3O2/c1-3-4-5-6-7-12(10(2)17)16-8-11(13(14)18)15-9-16/h8-10,12,17H,3-7H2,1-2H3,(H2,14,18)/t10-,12+/m0/s1

130573-54-5SDS

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 1-(2-hydroxynonan-3-yl)imidazole-4-carboxamide

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:130573-54-5 SDS

130573-54-5Downstream Products

130573-54-5Relevant academic research and scientific papers

Adenosine deaminase inhibitors: Synthesis and structure-activity relationships of imidazole analogues of erythro-9-(2-hydroxy-3-nonyl)adenine

Cristalli,Eleuteri,Franchetti,Grifantini,Vittori,Lupidi

, p. 1187 - 1192 (2007/10/02)

A series of erythro-1-(2-hydroxy-3-nonyl)imidazole derivatives have been synthesized and evaluated for adenosine deaminase (ADA) inhibitory activity, in order to introduce simplifications in the ADA inhibitors erythro-9-(2-hydroxy-3-nonyl)adenine (EHNA, 1

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