Cas no 39234-83-8 (4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride)
4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride Chemical and Physical Properties
Names and Identifiers
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- 4-Nitro-3-(trifluoromethyl)benzenesulphonyl chloride
- 4-nitro-3-(trifluoromethyl)Benzenesulfonyl chloride
- 4-nitro-3-(trifluoromethyl)benzene-1-sulfonyl chloride
- 4-nitro-3-(trifluoromethyl)-benzenesulfonyl chloride
- 4-nitro-3-(trifluoromethyl)phenylsulfonyl chloride
- 4-Nitro-3-trifluormethylphenylsulfonylchlorid
- AKOS015889615
- MFCD03094387
- 39234-83-8
- 4-nitro-3-(trifluoromethyl)benzenesulfonylchloride
- AS-46339
- CS-0157039
- CL9416
- SCHEMBL1422737
- AKOS005254674
- FT-0639537
- DTXSID20381020
- A824475
- 4-Nitro-3-(trifluoromethyl)benzenesulfonyl chloride, 97%
- DB-049394
- 4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride
-
- MDL： MFCD03094387
- Inchi： 1S/C7H3ClF3NO4S/c8-17(15,16)4-1-2-6(12(13)14)5(3-4)7(9,10)11/h1-3H
- InChI Key： LJQUNSRHHHYXEW-UHFFFAOYSA-N
- SMILES： ClS(C1=CC=C(C(C(F)(F)F)=C1)[N+](=O)[O-])(=O)=O
- BRN： 2880842
Computed Properties
- Exact Mass: 288.94200
- Monoisotopic Mass: 288.942
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 7
- Heavy Atom Count: 17
- Rotatable Bond Count: 1
- Complexity: 399
- 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
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: nothing
- Topological Polar Surface Area: 88.3A^2
Experimental Properties
- Color/Form: solid
- Density: 1.689
- Melting Point: 63-67?°C (lit.)
- Boiling Point: 354°Cat760mmHg
- Flash Point: 167.9°C
- Refractive Index: 1.511
- PSA: 88.34000
- LogP: 4.14510
- Solubility: Soluble
- Sensitiveness: Lachrymatory
4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride Security Information
-
Symbol:
- Signal Word：Danger
- Hazard Statement： H314
- Warning Statement： P280-P305+P351+P338-P310
- Hazardous Material transportation number：UN 3261 8/PG 2
- WGK Germany：3
- Hazard Category Code： 34
- Safety Instruction： S26-S36/37/39-S45
-
Hazardous Material Identification：
- HazardClass：8
- PackingGroup：II
- Safety Term：8
- Packing Group：II
- Risk Phrases：R34
4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride Customs Data
- HS CODE：2904909090
- Customs Data：
China Customs Code:
2904909090Overview:
2904909090 Sulfonation of other hydrocarbons\nitrification\Nitrosative derivative(Whether halogenated or not). VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:5.5% general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
HS:2904909090 sulphonated, nitrated or nitrosated derivatives of hydrocarbons, whether or not halogenated VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%
4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-RB556-5g |
4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride |
39234-83-8 | 95+% | 5g |
1946.0CNY | 2021-07-14 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-RB556-200mg |
4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride |
39234-83-8 | 95+% | 200mg |
168.0CNY | 2021-07-14 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-RB556-1g |
4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride |
39234-83-8 | 95+% | 1g |
522.0CNY | 2021-07-14 | |
| TRC | N233220-500mg |
4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride |
39234-83-8 | 500mg |
$ 220.00 | 2022-06-03 | ||
| TRC | N233220-1000mg |
4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride |
39234-83-8 | 1g |
$ 365.00 | 2022-06-03 | ||
| TRC | N233220-2000mg |
4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride |
39234-83-8 | 2g |
$ 580.00 | 2022-06-03 | ||
| Apollo Scientific | PC6567-250mg |
4-Nitro-3-(trifluoromethyl)benzenesulphonyl chloride |
39234-83-8 | 250mg |
￡10.00 | 2023-09-01 | ||
| Apollo Scientific | PC6567-1g |
4-Nitro-3-(trifluoromethyl)benzenesulphonyl chloride |
39234-83-8 | 1g |
￡70.00 | 2025-02-21 | ||
| Apollo Scientific | PC6567-5g |
4-Nitro-3-(trifluoromethyl)benzenesulphonyl chloride |
39234-83-8 | 5g |
￡225.00 | 2025-02-21 | ||
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | N89860-5g |
4-Nitro-3-(trifluoromethyl)benzene-1-sulfonyl chloride |
39234-83-8 | 95% | 5g |
￥496.0 | 2024-07-19 |
4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride Suppliers
Audited Supplier
4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride Related Literature
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1. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139
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Jacob S. Jordan,Evan R. Williams Analyst, 2021,146, 2617-2625
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Joo Chuan Yeo,Kenry Lab Chip, 2016,16, 4082-4090
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Jason Wan Lab Chip, 2020,20, 4528-4538
Additional information on 4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride
4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride: A Comprehensive Overview
4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride, also known by its CAS number 39234-83-8, is a highly specialized organic compound with significant applications in various fields of chemistry. This compound is characterized by its unique structure, which includes a benzenesulfonyl group substituted with a nitro group at the 4-position and a trifluoromethyl group at the 3-position. The combination of these substituents imparts distinctive chemical properties, making it valuable for research and industrial purposes.
The molecular structure of 4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride consists of a benzene ring with three key substituents: a sulfonyl chloride group (-SO?Cl), a nitro group (-NO?), and a trifluoromethyl group (-CF?). The sulfonyl chloride group is highly reactive, making it a versatile building block in organic synthesis. The nitro group introduces electron-withdrawing effects, enhancing the electrophilic character of the molecule, while the trifluoromethyl group contributes to both steric and electronic effects, further modulating the compound's reactivity.
Recent studies have highlighted the importance of 4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride in the development of advanced materials and pharmaceuticals. For instance, researchers have explored its role in synthesizing bioactive molecules with potential applications in drug discovery. The compound's ability to participate in nucleophilic aromatic substitution reactions has been extensively studied, with findings published in leading journals such as Journal of Medicinal Chemistry and Organic Letters.
In terms of synthesis, 4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride is typically prepared via multi-step processes involving sulfonation and subsequent substitution reactions. Recent advancements in catalytic methods have improved the efficiency and selectivity of these reactions, reducing production costs and minimizing environmental impact. These developments are particularly relevant for industries focused on fine chemicals and specialty materials.
The application of 4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride extends beyond traditional organic synthesis. It has been utilized as an intermediate in the production of agrochemicals, where its reactivity and stability under various conditions are highly advantageous. Additionally, its role in polymer chemistry has been explored, with researchers investigating its potential as a crosslinking agent or as part of functional polymers.
In conclusion, 4-Nitro-3-(Trifluoromethyl)Benzenesulfonyl Chloride, CAS No. 39234-83-8, stands as a pivotal compound in modern chemistry. Its unique structure and reactivity make it indispensable for both academic research and industrial applications. As ongoing research continues to uncover new potentials for this compound, its significance in the chemical landscape is expected to grow further.
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