Cas no 66695-96-3 (3-(3-Aminophenyl)-1-phenylurea)

3-(3-Aminophenyl)-1-phenylurea structure
66695-96-3 structure
Product Name:3-(3-Aminophenyl)-1-phenylurea
CAS No:66695-96-3
MF:C13H13N3O
MW:227.261822462082
MDL:MFCD08532932
CID:522228
PubChem ID:302843
Update Time:2025-04-23

3-(3-Aminophenyl)-1-phenylurea Chemical and Physical Properties

Names and Identifiers

    • Urea,N-(3-aminophenyl)-N'-phenyl-
    • 1-(3-aminophenyl)-3-phenylurea
    • N-(3-AMINOPHENYL)-N''-PHENYLUREA
    • N-(3-AMINOPHENYL)-N'-PHENYLUREA
    • N-(3-Amino-phenyl)-N'-phenyl-harnstoff
    • N-(3-amino-phenyl)-N'-phenyl-urea
    • N-phenyl-N'-(3-aminophenyl)-urea
    • 1-(3-Amino-phenyl)-3-phenyl-urea
    • DTXSID00307263
    • AKOS000264076
    • N-(3-AMINOPHENYL)-N-PHENYLUREA
    • EN300-26799
    • NSC190579
    • CHEMBL9418
    • 66695-96-3
    • 3-(3-aminophenyl)-1-phenylurea
    • HEPNAISIYKJLIZ-UHFFFAOYSA-N
    • NSC-190579
    • 1-(3-aminophenyl)-3-phenyl urea
    • SCHEMBL711068
    • Z234815906
    • 3-(3-Aminophenyl)-1-phenylurea
    • MDL: MFCD08532932
    • Inchi: 1S/C13H13N3O/c14-10-5-4-8-12(9-10)16-13(17)15-11-6-2-1-3-7-11/h1-9H,14H2,(H2,15,16,17)
    • InChI Key: HEPNAISIYKJLIZ-UHFFFAOYSA-N
    • SMILES: O=C(NC1C=CC=CC=1)NC1C=CC=C(C=1)N

Computed Properties

  • Exact Mass: 227.10600
  • Monoisotopic Mass: 227.106
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 4
  • Complexity: 251
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.3
  • Topological Polar Surface Area: 67.2?2

Experimental Properties

  • Density: 1.32
  • Boiling Point: 321.2°C at 760 mmHg
  • Flash Point: 148°C
  • Refractive Index: 1.738
  • PSA: 67.15000
  • LogP: 3.64000

3-(3-Aminophenyl)-1-phenylurea Customs Data

  • HS CODE:2924299090
  • Customs Data:

    China Customs Code:

    2924299090

    Overview:

    2924299090. Other cyclic amides(Including cyclic carbamates)(Including their derivatives as well as their salts). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to, packing

    Summary:

    2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

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Additional information on 3-(3-Aminophenyl)-1-phenylurea

Introduction to Urea, N-(3-aminophenyl)-N'-phenyl- (CAS No. 66695-96-3)

Urea, N-(3-aminophenyl)-N'-phenyl- (CAS No. 66695-96-3) is a significant compound in the field of chemical and pharmaceutical research. This compound, characterized by its unique molecular structure, has garnered considerable attention due to its potential applications in various scientific domains. The molecular formula of this compound can be represented as C13H14N2O, which underscores its complexity and the diverse interactions it can exhibit with other molecules.

The primary focus of this introduction is to delve into the properties, synthesis, and emerging applications of Urea, N-(3-aminophenyl)-N'-phenyl-. By examining the latest research findings, we aim to provide a comprehensive understanding of how this compound is being utilized in contemporary scientific endeavors. The discussion will cover its chemical characteristics, synthetic pathways, and its role in pharmaceutical development and biochemical studies.

In recent years, the interest in Urea, N-(3-aminophenyl)-N'-phenyl- has surged due to its versatile reactivity and structural features. This compound serves as a crucial intermediate in the synthesis of more complex molecules, making it invaluable in organic chemistry. Its ability to participate in various chemical reactions, such as condensation and cyclization, allows for the creation of novel derivatives with tailored properties.

The synthesis of Urea, N-(3-aminophenyl)-N'-phenyl- typically involves the reaction between 3-aminophenylamine and phenylurea under controlled conditions. These conditions are meticulously optimized to ensure high yield and purity. The process often requires careful temperature control and the use of appropriate catalysts to facilitate the reaction. Advances in synthetic methodologies have enabled researchers to produce this compound with greater efficiency and scalability.

One of the most compelling aspects of Urea, N-(3-aminophenyl)-N'-phenyl- is its potential application in pharmaceuticals. Researchers are exploring its use as a precursor in the development of new drugs that target various diseases. Its molecular structure allows for modifications that can enhance binding affinity to biological targets, making it a promising candidate for drug design. For instance, studies have shown that derivatives of this compound exhibit inhibitory effects on certain enzymes involved in metabolic pathways.

The biochemical properties of Urea, N-(3-aminophenyl)-N'-phenyl- have also attracted attention in the field of medicinal chemistry. Its ability to interact with biological molecules suggests that it could be used to develop novel therapeutic agents. Additionally, its role as a scaffold for drug design has opened up new avenues for research. By modifying its structure, scientists can create compounds with improved pharmacological profiles.

In conclusion, Urea, N-(3-aminophenyl)-N'-phenyl- (CAS No. 66695-96-3) is a multifaceted compound with significant implications in chemical and pharmaceutical research. Its unique properties make it a valuable tool for synthesizing complex molecules and developing new drugs. As research continues to uncover its potential applications, this compound is poised to play an increasingly important role in advancing scientific knowledge and innovation.

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