Cas no 6317-57-3 (4-Benzylaniline)
4-Benzylaniline Chemical and Physical Properties
Names and Identifiers
-
- 4-Benzylaniline hydrochloride
- 4-AMINODIPHENYLMETHANE
- 4-Benzylaniline, HCl
- 4-Benzyl-phenylamine hydrochloride
- Benzenamine,4-(phenylmethyl)-, hydrochloride (1:1)
- 4-BENZYLANILINE
- p-Toluidine, alpha-phenyl-, hydrochloride
- AKOS005287364
- NSC 43061
- NSC43061
- 4-BENZYLANILINE HCL
- Benzenamine, 4-(phenylmethyl)-, hydrochloride
- 4-benzylaniline;hydrochloride
- NSC-43061
- (4-benzylphenyl)amine hydrochloride
- AS-59981
- 4-(Phenylmethyl)benzenamine hydrochloride
- SB79474
- SCHEMBL8746107
- 4-benzylanilinehydrochloride
- alpha-Phenyl-p-toluidine hydrochloride
- 6317-57-3
- p-aminodiphenyl-methane hydrochloride
- 4-Benzylaniline
-
- MDL： MFCD01679497
- Inchi： 1S/C13H13N.ClH/c14-13-8-6-12(7-9-13)10-11-4-2-1-3-5-11;/h1-9H,10,14H2;1H
- InChI Key： GQGXIDBMRPMPCD-UHFFFAOYSA-N
- SMILES： Cl.NC1C=CC(=CC=1)CC1C=CC=CC=1
Computed Properties
- Exact Mass: 183.10500
- Monoisotopic Mass: 219.081
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 15
- Rotatable Bond Count: 2
- Complexity: 153
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 26A^2
Experimental Properties
- Melting Point: 219 oC
- Boiling Point: 300°C at 760 mmHg
- Flash Point: >230?°F
- PSA: 26.02000
- LogP: 3.44080
- pka: 2.17(at 25℃)
4-Benzylaniline Customs Data
- HS CODE：2921420090
- Customs Data：
China Customs Code:
2921420090Overview:
2921420090 Other aniline derivatives and their salts. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
HS:2921420090 aniline derivatives and their salts VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%
4-Benzylaniline Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | B230010-5mg |
4-Benzylaniline |
6317-57-3 | 5mg |
$ 50.00 | 2022-06-07 | ||
| TRC | B230010-10mg |
4-Benzylaniline |
6317-57-3 | 10mg |
$ 65.00 | 2022-06-07 | ||
| TRC | B230010-50mg |
4-Benzylaniline |
6317-57-3 | 50mg |
$ 115.00 | 2022-06-07 | ||
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | B857737-1g |
4-Benzylaniline |
6317-57-3 | ≥98% | 1g |
￥202.50 | 2022-09-02 | |
| eNovation Chemicals LLC | K95569-1g |
4-Benzylaniline |
6317-57-3 | 97% | 1g |
$200 | 2023-09-03 | |
| eNovation Chemicals LLC | D955925-25g |
4-Benzylaniline hydrochloride |
6317-57-3 | 98% | 25g |
$335 | 2023-09-04 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1536683-1g |
4-Benzylaniline hydrochloride |
6317-57-3 | 98% | 1g |
￥193.00 | 2024-05-06 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1536683-5g |
4-Benzylaniline hydrochloride |
6317-57-3 | 98% | 5g |
￥592.00 | 2024-05-06 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1536683-25g |
4-Benzylaniline hydrochloride |
6317-57-3 | 98% | 25g |
￥2295.00 | 2024-05-06 | |
| Ambeed | A772078-25g |
4-Benzylaniline hydrochloride |
6317-57-3 | 95+% | 25g |
$212.0 | 2024-04-18 |
4-Benzylaniline Suppliers
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4-Benzylaniline Related Literature
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Xiaoming Liu,Zachary D. Hood,Wangda Li,Donovan N. Leonard,Arumugam Manthiram,Miaofang Chi J. Mater. Chem. A, 2021,9, 2111-2119
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Danlei Xiang Nanoscale, 2021,13, 5497-5506
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Bo Chen,Xiaotong Shen,Zhangfeng Luo,Di Cai,Changjing Chen,Changwei Zhang,Peiyong Qin,Hui Cao,Tianwei Tan RSC Adv., 2018,8, 25602-25610
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Saeideh Mirfakhraei,Malak Hekmati,Fereshteh Hosseini Eshbala,Hojat Veisi New J. Chem., 2018,42, 1757-1761
Additional information on 4-Benzylaniline
4-Benzylaniline: A Comprehensive Overview
4-Benzylaniline (CAS No. 6317-57-3) is a significant compound in the field of organic chemistry, particularly within the aromatic amine family. This compound, also referred to as para-benzylaniline, is widely recognized for its unique chemical properties and diverse applications. The benzylamine group attached to the aromatic ring contributes to its reactivity and versatility, making it a valuable intermediate in various chemical syntheses.
Recent studies have highlighted the importance of 4-Benzylaniline in the development of advanced materials, such as high-performance polymers and optoelectronic devices. Researchers have explored its role in forming stable covalent bonds with other functional groups, enabling the creation of materials with enhanced thermal stability and mechanical strength. For instance, a 2023 study published in *Chemical Reviews* demonstrated how 4-Benzylaniline can be used as a building block for synthesizing polyaromatic compounds with applications in flexible electronics.
The synthesis of 4-Benzylaniline typically involves nucleophilic substitution reactions, where the amine group acts as a nucleophile attacking an activated benzyl halide. This reaction is highly efficient under controlled conditions, yielding high-purity products suitable for industrial applications. Moreover, advancements in catalytic methods have further optimized the synthesis process, reducing production costs and environmental impact.
In terms of applications, 4-Benzylaniline finds extensive use in pharmaceuticals, agrochemicals, and specialty chemicals. Its ability to form stable Schiff bases with carbonyl compounds has made it a key intermediate in drug discovery programs targeting various therapeutic areas, including oncology and neurodegenerative diseases. A notable example is its role in the synthesis of certain kinase inhibitors, which are currently under clinical evaluation for cancer treatment.
Another emerging application of 4-Benzylaniline is in the field of green chemistry. Scientists have leveraged its reactivity to develop eco-friendly processes for producing biodegradable polymers. For instance, a 2023 research article in *Green Chemistry* reported the successful use of 4-Benzylaniline as a precursor for synthesizing polyurethanes with improved biodegradation rates, addressing concerns related to plastic waste.
The chemical structure of 4-Benzylaniline plays a pivotal role in its reactivity and functionality. The presence of the benzyl group at the para position ensures minimal steric hindrance, facilitating smooth reactions with electrophiles and nucleophiles alike. Additionally, the resonance stabilization provided by the aromatic ring enhances its stability under harsh reaction conditions.
From an analytical standpoint, modern techniques such as high-resolution mass spectrometry (HRMS) and nuclear magnetic resonance (NMR) spectroscopy have enabled precise characterization of 4-Benzylaniline. These tools have been instrumental in confirming its molecular structure and purity, ensuring consistent quality across different production batches.
In conclusion, 4-Benzylaniline (CAS No. 6317-57-3) stands as a versatile compound with significant contributions to various scientific domains. Its unique chemical properties, coupled with ongoing advancements in synthesis and application techniques, continue to expand its utility across industries. As research progresses, it is anticipated that 4-Benzylaniline will play an even more prominent role in shaping future innovations in materials science and pharmaceutical development.
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