Cas no 24477-92-7 (Methyl 4-(4-aminophenoxy)benzoate)
Methyl 4-(4-aminophenoxy)benzoate Chemical and Physical Properties
Names and Identifiers
-
- Benzoic acid, 4-(4-aminophenoxy)-, methyl ester
- METHYL 4-(4-AMINOPHENOXY)BENZOATE
- 4-(4-Amino-phenoxy)-benzoesaeure-methylester
- 4-(4-amino-phenoxy)-benzoic acid methyl ester
- 4-Methoxycarbonyl-4'-amino-diphenyloxid
- AG-B-27749
- BB 0237266
- CTK6J0072
- KB-256716
- SureCN4242980
- ZAA47792
- 24477-92-7
- METHYL4-(4-AMINOPHENOXY)BENZOATE
- DKBOFXZTTWKXQL-UHFFFAOYSA-N
- DB-351982
- EN300-7410713
- 4-(4-aminophenoxy)-benzoic acid methyl ester
- DTXSID10619869
- AB7447
- BS-27812
- CS-0188255
- SCHEMBL4242980
- MFCD00445273
- AKOS000346158
- Methyl 4-(4-aminophenoxy)benzoate
-
- MDL: MFCD00445273
- Inchi: 1S/C14H13NO3/c1-17-14(16)10-2-6-12(7-3-10)18-13-8-4-11(15)5-9-13/h2-9H,15H2,1H3
- InChI Key: DKBOFXZTTWKXQL-UHFFFAOYSA-N
- SMILES: O(C1C=CC(=CC=1)N)C1C=CC(C(=O)OC)=CC=1
Computed Properties
- Exact Mass: 243.08959
- Monoisotopic Mass: 243.08954328g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 18
- Rotatable Bond Count: 4
- Complexity: 266
- 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: 2.9
- Topological Polar Surface Area: 61.6?2
Experimental Properties
- PSA: 61.55
Methyl 4-(4-aminophenoxy)benzoate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 022466-1g |
Methyl 4-(4-aminophenoxy)benzoate |
24477-92-7 | 1g |
5379CNY | 2021-05-07 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 022466-5g |
Methyl 4-(4-aminophenoxy)benzoate |
24477-92-7 | 5g |
15361CNY | 2021-05-07 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 022466-500mg |
Methyl 4-(4-aminophenoxy)benzoate |
24477-92-7 | 500mg |
3332CNY | 2021-05-07 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 022466-1g |
Methyl 4-(4-aminophenoxy)benzoate |
24477-92-7 | 1g |
5379.0CNY | 2021-07-05 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 022466-5g |
Methyl 4-(4-aminophenoxy)benzoate |
24477-92-7 | 5g |
15361.0CNY | 2021-07-05 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 022466-500mg |
Methyl 4-(4-aminophenoxy)benzoate |
24477-92-7 | 500mg |
3332.0CNY | 2021-07-10 | ||
| TRC | M328733-25mg |
Methyl 4-(4-aminophenoxy)benzoate |
24477-92-7 | 25mg |
$64.00 | 2023-05-17 | ||
| TRC | M328733-50mg |
Methyl 4-(4-aminophenoxy)benzoate |
24477-92-7 | 50mg |
$69.00 | 2023-05-17 | ||
| TRC | M328733-100mg |
Methyl 4-(4-aminophenoxy)benzoate |
24477-92-7 | 100mg |
$98.00 | 2023-05-17 | ||
| TRC | M328733-250mg |
Methyl 4-(4-aminophenoxy)benzoate |
24477-92-7 | 250mg |
$167.00 | 2023-05-17 |
Methyl 4-(4-aminophenoxy)benzoate Related Literature
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Yang Chen,Di Zhou,Zheyi Meng,Jin Zhai Chem. Commun., 2016,52, 10020-10023
-
Kaiyuan Huang,Wangkang Qiu,Meilian Ou,Xiaorui Liu,Zenan Liao,Sheng Chu RSC Adv., 2020,10, 18824-18829
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Teresita Carrillo-Hernández,Philippe Schaeffer,Pierre Albrecht Chem. Commun., 2001, 1976-1977
-
Yu-Nong Li,Liang-Nian He,Xian-Dong Lang,Xiao-Fang Liu,Shuai Zhang RSC Adv., 2014,4, 49995-50002
Additional information on Methyl 4-(4-aminophenoxy)benzoate
Methyl 4-(4-aminophenoxy)benzoate (CAS No. 24477-92-7): A Comprehensive Overview
Methyl 4-(4-aminophenoxy)benzoate, also known by its CAS number 24477-92-7, is a versatile organic compound with significant applications in various fields of chemistry and materials science. This compound, characterized by its unique structure, has garnered attention in recent years due to its potential in drug design, polymer synthesis, and as an intermediate in the production of advanced materials. In this article, we delve into the structural properties, chemical characteristics, and emerging applications of Methyl 4-(4-aminophenoxy)benzoate, supported by the latest research findings.
The molecular structure of Methyl 4-(4-aminophenoxy)benzoate consists of a benzoate ester group attached to a phenoxy ring, which is further substituted with an amino group at the para position. This arrangement imparts the compound with unique electronic and steric properties. The presence of the amino group introduces nucleophilic character, while the ester functionality provides opportunities for further functionalization. Recent studies have highlighted the importance of such structural features in enhancing the compound's reactivity and compatibility in diverse chemical systems.
From a chemical standpoint, Methyl 4-(4-aminophenoxy)benzoate exhibits interesting physical and chemical properties. Its melting point and solubility characteristics make it suitable for various synthetic routes. Moreover, the compound demonstrates moderate stability under standard conditions, though it can undergo hydrolysis under acidic or basic conditions to yield corresponding carboxylic acids or their salts. These properties have been extensively explored in recent research to optimize its use as an intermediate in organic synthesis.
The applications of Methyl 4-(4-aminophenoxy)benzoate span across multiple domains. In pharmaceutical chemistry, it has been employed as a building block for designing bioactive molecules targeting specific therapeutic areas. For instance, researchers have utilized its amino group to facilitate the construction of peptide-like structures with potential medicinal value. Additionally, its phenoxy group has been leveraged in the development of novel polymer materials with enhanced mechanical and thermal properties.
In recent years, there has been a growing interest in exploring the use of Methyl 4-(4-aminophenoxy)benzoate as an intermediate in the synthesis of advanced materials such as liquid crystals and optical polymers. Its ability to form hydrogen bonds and its planar aromatic structure contribute to these applications. Studies have demonstrated that derivatives of this compound can exhibit desirable liquid crystalline properties, making them candidates for next-generation display technologies.
From an environmental perspective, understanding the fate and behavior of Methyl 4-(4-aminophenoxy)benzoate in natural systems is crucial for assessing its potential impact on ecosystems. Recent research has focused on evaluating its biodegradation pathways under aerobic and anaerobic conditions. These studies aim to provide insights into sustainable practices for handling and disposing of this compound.
In conclusion, Methyl 4-(4-aminophenoxy)benzoate (CAS No. 24477-92-7) stands out as a multifaceted compound with promising applications across various scientific disciplines. Its unique structure and chemical properties continue to drive innovative research efforts aimed at unlocking its full potential. As advancements in synthetic methodologies and material science progress, this compound is poised to play an increasingly significant role in both academic and industrial settings.
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