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2,4-IMIDAZOLIDINEDIONE, 3-(3-AMINO-1-OXOPROPYL)-1-(((5-(3,4-DICHLOROPH ENYL)-2-FU is a complex organic compound characterized by the presence of an imidazolidinedione ring, an amino group, a ketone group, and a dichlorophenyl moiety. The combination of these functional groups likely endows 2,4-IMIDAZOLIDINEDIONE, 3-(3-AMINO-1-OXOPROPYL)-1-(((5-(3,4-DICHLOROPH ENYL)-2-FU with a range of biological and chemical properties, making it suitable for various applications in research and industry. However, more information is needed to fully understand its specific uses, effects, and potential hazards.

79962-63-3

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79962-63-3 Usage

Uses

Used in Pharmaceutical Industry:
2,4-IMIDAZOLIDINEDIONE, 3-(3-AMINO-1-OXOPROPYL)-1-(((5-(3,4-DICHLOROPH ENYL)-2-FU is used as a pharmaceutical intermediate for the synthesis of various drugs and drug candidates. Its unique structure and functional groups may contribute to the development of new therapeutic agents with novel mechanisms of action.
Used in Chemical Research:
2,4-IMIDAZOLIDINEDIONE, 3-(3-AMINO-1-OXOPROPYL)-1-(((5-(3,4-DICHLOROPH ENYL)-2-FU is utilized in chemical research for studying the properties and reactivity of imidazolidinedione, amino, and ketone groups, as well as the influence of dichlorophenyl substitution on the compound's behavior. It may also serve as a starting material for the synthesis of more complex molecules with potential applications in various fields.
Used in Agrochemical Industry:
2,4-IMIDAZOLIDINEDIONE, 3-(3-AMINO-1-OXOPROPYL)-1-(((5-(3,4-DICHLOROPH ENYL)-2-FU may be employed as an agrochemical intermediate, potentially contributing to the development of new pesticides or herbicides. Its specific mode of action and target pests or weeds would depend on further research and development.
Used in Material Science:
2,4-IMIDAZOLIDINEDIONE, 3-(3-AMINO-1-OXOPROPYL)-1-(((5-(3,4-DICHLOROPH ENYL)-2-FU's unique structure and functional groups may also find applications in material science, such as in the development of new polymers, coatings, or adhesives with specific properties. Further research would be required to explore these potential applications and optimize the compound's performance in these areas.

Check Digit Verification of cas no

The CAS Registry Mumber 79962-63-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,9,6 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79962-63:
(7*7)+(6*9)+(5*9)+(4*6)+(3*2)+(2*6)+(1*3)=193
193 % 10 = 3
So 79962-63-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H14Cl2N4O4.ClH/c18-12-3-1-10(7-13(12)19)14-4-2-11(27-14)8-21-22-9-16(25)23(17(22)26)15(24)5-6-20;/h1-4,7-8H,5-6,9,20H2;1H/b21-8+;

79962-63-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-[3-[(E)-[5-(3,4-dichlorophenyl)furan-2-yl]methylideneamino]-2,5-dioxoimidazolidin-1-yl]-3-oxopropyl]azanium,chloride

1.2 Other means of identification

Product number -
Other names 2,4-Imidazolidinedione,3-(3-amino-1-oxopropyl)-1-(((5-(3,4-dichlorophenyl)-2-furanyl)methylene)amino)-,monohydrochloride

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:79962-63-3 SDS

79962-63-3Downstream Products

79962-63-3Relevant academic research and scientific papers

Synthesis and skeletal muscle relaxant activity of 3-(aminoacyl)-1-[[[5-(substituted phenyl)-2-furanyl]methylene]amino]-2,4-imidazolidinediones

Wessels,Ellis,White Jr.

, p. 1088 - 1090 (2007/10/02)

A series of 3-(aminoacyl)-1-[[[5-(substituted phenyl)-2-furanyl]methylene]amino]-2,4-imidazolidinediones was synthesized and evaluated for skeletal muscle relaxant activity. All compounds were active by the intravenous route, and nine of 11 were active orally. One compound was very active when evaluated by the mouse Straub tail and rotarod tests; its efficacy index (ED50 rotarod/ED50Straub tail) was 2.0, while its therapeutic index (LD50/ED50Straub tail) was >225.

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