Cas no 20731-63-9 (4-Chloro-3,5-dinitrobenzamide)
4-Chloro-3,5-dinitrobenzamide Chemical and Physical Properties
Names and Identifiers
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- Benzamide,4-chloro-3,5-dinitro-
- 4-CHLORO-3,5-DINITROBENZAMIDE
- 3.5-Dinitro-4-chlor-benzamid
- 4-Chlor-3,5-dinitro-benzoesaeure-amid
- 4-Chlor-3.5-dinitro-benzamid
- 4-chloro-3,5-dinitro-benzoic acid amide
- AC1L3G8O
- Benzamide,4-chloro-3,5-dinitro
- CTK4E4963
- EINECS 243-998-5
- CS-0360355
- DTXSID70174803
- 4-CHLORO-3,5-DINITROBENZ-AMIDE
- Benzamide, 4-chloro-3,5-dinitro-
- NSC 76582
- NS00026723
- AKOS005434470
- FT-0722093
- SCHEMBL6570802
- C7H4ClN3O5
- WP9P28GYV2
- XIYABENEBOSULF-UHFFFAOYSA-N
- 3,5-DINITRO-4-CHLOROBENZAMIDE
- NSC76582
- NSC-76582
- 20731-63-9
- 4-Chloro-3,5-dinitrobenzamide
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- Inchi： 1S/C7H4ClN3O5/c8-6-4(10(13)14)1-3(7(9)12)2-5(6)11(15)16/h1-2H,(H2,9,12)
- InChI Key： XIYABENEBOSULF-UHFFFAOYSA-N
- SMILES： ClC1=C(C=C(C(N)=O)C=C1[N+](=O)[O-])[N+](=O)[O-]
Computed Properties
- Exact Mass: 244.98400
- Monoisotopic Mass: 244.9839479g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 16
- Rotatable Bond Count: 3
- Complexity: 301
- 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: 1.8
- Topological Polar Surface Area: 135?2
Experimental Properties
- PSA: 134.73000
- LogP: 3.00200
4-Chloro-3,5-dinitrobenzamide Customs Data
- HS CODE：2924299090
- Customs Data：
China Customs Code:
2924299090Overview:
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%
4-Chloro-3,5-dinitrobenzamide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | C381928-50mg |
4-Chloro-3,5-dinitrobenzamide |
20731-63-9 | 50mg |
$ 50.00 | 2022-06-06 | ||
| TRC | C381928-100mg |
4-Chloro-3,5-dinitrobenzamide |
20731-63-9 | 100mg |
$ 65.00 | 2022-06-06 | ||
| TRC | C381928-500mg |
4-Chloro-3,5-dinitrobenzamide |
20731-63-9 | 500mg |
$ 115.00 | 2022-06-06 | ||
| A2B Chem LLC | AB17711-100mg |
Benzamide, 4-chloro-3,5-dinitro- |
20731-63-9 | 95% | 100mg |
$53.00 | 2024-04-20 | |
| 1PlusChem | 1P002JFZ-100mg |
Benzamide, 4-chloro-3,5-dinitro- |
20731-63-9 | 95% | 100mg |
$53.00 | 2025-02-19 |
4-Chloro-3,5-dinitrobenzamide Suppliers
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4-Chloro-3,5-dinitrobenzamide Related Literature
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1. The dipole moments, molar Kerr constants, and solution-state conformations of some substituted benzamidesRaymond K. Pierens,Alan J. Williams J. Chem. Soc. Perkin Trans. 2 1980 235
Additional information on 4-Chloro-3,5-dinitrobenzamide
4-Chloro-3,5-dinitrobenzamide (CAS No. 20731-63-9): A Comprehensive Overview of Its Properties and Applications
4-Chloro-3,5-dinitrobenzamide (CAS No. 20731-63-9) is a specialized organic compound that has garnered significant attention in the fields of chemical synthesis, agricultural chemistry, and material science. This compound, characterized by its nitrobenzamide backbone, is widely recognized for its unique chemical properties and versatile applications. In this article, we delve into the molecular structure, synthesis methods, and potential uses of 4-Chloro-3,5-dinitrobenzamide, while also addressing common queries and trends in the scientific community.
The molecular formula of 4-Chloro-3,5-dinitrobenzamide is C7H4ClN3O5, and it features a chloro-substituted benzene ring with two nitro groups at the 3 and 5 positions. This structural configuration imparts distinct reactivity, making it a valuable intermediate in organic synthesis. Researchers often explore its role in the development of agrochemicals and pharmaceutical precursors, as its electron-withdrawing groups enhance its suitability for nucleophilic substitution reactions.
One of the most frequently searched questions about 4-Chloro-3,5-dinitrobenzamide revolves around its synthesis pathways. The compound is typically synthesized through the nitration of 4-chlorobenzamide, followed by careful purification to achieve high yields. Recent advancements in green chemistry have also prompted investigations into eco-friendly synthesis methods, such as catalytic nitration using biodegradable reagents. These innovations align with the growing demand for sustainable chemical processes in industrial applications.
In the agricultural sector, 4-Chloro-3,5-dinitrobenzamide has been studied for its potential as a herbicide intermediate. Its ability to disrupt plant metabolic pathways makes it a candidate for developing next-generation crop protection agents. However, researchers emphasize the need for rigorous environmental impact assessments to ensure its safe use. This topic resonates with current debates on precision agriculture and the balance between productivity and ecological sustainability.
Another area of interest is the compound's role in material science. Due to its aromatic nitro groups, 4-Chloro-3,5-dinitrobenzamide can serve as a building block for high-performance polymers and explosive precursors (non-hazardous applications). Its thermal stability and compatibility with other monomers make it a subject of ongoing research in advanced material engineering.
Safety and handling of 4-Chloro-3,5-dinitrobenzamide are also critical topics. While not classified as a hazardous substance under standard regulations, proper laboratory protocols must be followed to minimize risks. This includes using personal protective equipment (PPE) and adhering to waste disposal guidelines. These precautions align with broader industry trends toward occupational health and safety in chemical research.
In conclusion, 4-Chloro-3,5-dinitrobenzamide (CAS No. 20731-63-9) is a multifaceted compound with promising applications across diverse fields. Its synthesis, agricultural potential, and material science relevance make it a subject of enduring scientific interest. As research continues to uncover new uses, this compound will likely remain a focal point in discussions about innovative chemistry and sustainable technology.
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