Cas no 24821-17-8 (2-Nitro-6-(trifluoromethyl)aniline)
2-Nitro-6-(trifluoromethyl)aniline Chemical and Physical Properties
Names and Identifiers
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- 2-Nitro-6-(trifluoromethyl)aniline
- 2-AMINO-3-NITROBENZOTRIFLUORIDE
- Benzenamine,2-nitro-6-(trifluoromethyl)-
- 2-Nitro-6-trifluormethyl-anilin
- 2-nitro-6-trifluoromethylaniline
- 2-nitro-6-trifluoromethyl-phenylamine
- 6-nitro-2-trifluoromethylaniline
- SB78572
- PS-10534
- 2-Amino-3-nitrobenzotrifluoride 99%
- DTXSID50443726
- Benzenamine, 2-nitro-6-(trifluoromethyl)-
- SCHEMBL1768922
- CL8407
- 2-Nitro-6-(trifluoromethyl)aniline, 97%
- MFCD08532494
- 2-nitro-6-trifluoromethyl aniline
- AKOS015999907
- J-015687
- 24821-17-8
- EN300-127182
- AKOS015912862
- DB-365204
- 2-amino-3-trifluoromethylnitrobenzene
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- MDL: MFCD08532494
- Inchi: 1S/C7H5F3N2O2/c8-7(9,10)4-2-1-3-5(6(4)11)12(13)14/h1-3H,11H2
- InChI Key: MFLJFFUIURSSKM-UHFFFAOYSA-N
- SMILES: FC(C1C=CC=C(C=1N)[N+](=O)[O-])(F)F
Computed Properties
- Exact Mass: 206.03000
- Monoisotopic Mass: 206.03031189g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 14
- Rotatable Bond Count: 2
- Complexity: 226
- 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: 2.5
- Topological Polar Surface Area: 71.8?2
Experimental Properties
- Color/Form: No data available
- Density: 1.503±0.06 g/cm3 (20 oC 760 Torr),
- Melting Point: 48-52?°C
- Boiling Point: 261.1±35.0 oC (760 Torr),
- Flash Point: Degrees Fahrenheit:>230°F
Degrees Celsius:>110°C - Refractive Index: 1.525
- Solubility: Very slightly soluble (0.17 g/l) (25 o C),
- PSA: 71.84000
- LogP: 3.30020
2-Nitro-6-(trifluoromethyl)aniline Security Information
- Signal Word:warning
- Hazard Statement: Harmful
-
Warning Statement:
P264Thoroughly clean after treatment
P280Wear protective gloves/Wear protective clothing/Wear protective goggles/Wear a protective mask
P305If it enters the eyes
P351Rinse carefully with water for a few minutes
P338Remove the contact lens(If any)And easy to operate,Continue flushing
P337If eye irritation persists
P313Obtain medical advice/care - Hazardous Material transportation number:NONH for all modes of transport
- WGK Germany:3
- Safety Instruction: H303May be harmful if swallowed+H313Skin contact may be harmful+H333Inhalation may be harmful to the body
- Storage Condition:Store at 4°C,-4At ℃Store…Better
2-Nitro-6-(trifluoromethyl)aniline 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%
2-Nitro-6-(trifluoromethyl)aniline Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | L-HJ181-1g |
2-Nitro-6-(trifluoromethyl)aniline |
24821-17-8 | 97% | 1g |
¥1221.0 | 2022-09-28 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | L-HJ181-200mg |
2-Nitro-6-(trifluoromethyl)aniline |
24821-17-8 | 97% | 200mg |
¥400.0 | 2022-09-28 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBTYC0938-1 G |
2-nitro-6-(trifluoromethyl)aniline |
24821-17-8 | 95% | 1g |
¥ 686.00 | 2021-05-07 | |
| NAN JING YAO SHI KE JI GU FEN Co., Ltd. | PBTYC0938-5 G |
2-nitro-6-(trifluoromethyl)aniline |
24821-17-8 | 95% | 5g |
¥ 2,072.00 | 2021-05-07 | |
| Chemenu | CM192235-5g |
2-nitro-6-(trifluoromethyl)aniline |
24821-17-8 | 95+% | 5g |
$430 | 2021-06-16 | |
| Chemenu | CM192235-10g |
2-nitro-6-(trifluoromethyl)aniline |
24821-17-8 | 95+% | 10g |
$818 | 2021-06-16 | |
| Alichem | A013006395-250mg |
2-Nitro-6-(trifluoromethyl)aniline |
24821-17-8 | 97% | 250mg |
$489.60 | 2023-09-02 | |
| Alichem | A013006395-500mg |
2-Nitro-6-(trifluoromethyl)aniline |
24821-17-8 | 97% | 500mg |
$831.30 | 2023-09-02 | |
| Alichem | A013006395-1g |
2-Nitro-6-(trifluoromethyl)aniline |
24821-17-8 | 97% | 1g |
$1519.80 | 2023-09-02 | |
| Apollo Scientific | PC5277-1g |
2-Amino-3-nitrobenzotrifluoride |
24821-17-8 | 99% | 1g |
£46.00 | 2025-02-21 |
2-Nitro-6-(trifluoromethyl)aniline Suppliers
2-Nitro-6-(trifluoromethyl)aniline Related Literature
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1. A convenient copper-catalyzed direct amination of nitroarenes with O-alkylhydroxylaminesShinzo Seko,Kunihito Miyake,Norio Kawamura J. Chem. Soc. Perkin Trans. 1 1999 1437
Additional information on 2-Nitro-6-(trifluoromethyl)aniline
Introduction to 2-Nitro-6-(trifluoromethyl)aniline (CAS No. 24821-17-8)
2-Nitro-6-(trifluoromethyl)aniline, with the CAS number 24821-17-8, is a versatile compound that has garnered significant attention in the fields of organic chemistry, pharmaceuticals, and materials science. This aromatic amine features a nitro group and a trifluoromethyl group, which endow it with unique chemical properties and reactivity. This introduction will delve into the chemical structure, synthesis methods, applications, and recent research advancements related to this compound.
The molecular formula of 2-Nitro-6-(trifluoromethyl)aniline is C9H6F3N2O2, and its molecular weight is approximately 213.15 g/mol. The presence of the nitro group (NO2) and the trifluoromethyl group (CF3) imparts strong electron-withdrawing properties to the molecule, making it highly reactive in various chemical reactions. The aromatic ring provides additional stability and reactivity, making this compound a valuable intermediate in the synthesis of more complex molecules.
The synthesis of 2-Nitro-6-(trifluoromethyl)aniline can be achieved through several methods. One common approach involves the nitration of 6-(trifluoromethyl)aniline using a mixture of nitric acid and sulfuric acid. This method is well-documented in the literature and has been optimized to achieve high yields and purity. Another method involves the reaction of 3-nitrobenzotrifluoride with ammonia in the presence of a suitable catalyst, such as palladium on carbon. This approach offers an alternative route that can be tailored to specific process requirements.
In the pharmaceutical industry, 2-Nitro-6-(trifluoromethyl)aniline has found applications as an intermediate in the synthesis of various drugs. Its unique chemical properties make it suitable for use in the development of compounds with specific biological activities. For example, recent studies have explored its potential in the synthesis of anti-cancer agents and anti-inflammatory drugs. The trifluoromethyl group enhances lipophilicity, which can improve drug absorption and distribution in biological systems.
Beyond pharmaceuticals, 2-Nitro-6-(trifluoromethyl)aniline has also been investigated for its use in materials science. Its strong electron-withdrawing properties make it a valuable component in the development of electronic materials, such as organic semiconductors and dyes for photovoltaic applications. Research in this area has shown that compounds derived from 2-Nitro-6-(trifluoromethyl)aniline can exhibit improved charge transport properties and stability under various environmental conditions.
The environmental impact of chemicals is an important consideration in their development and application. Studies on the environmental fate and toxicity of 2-Nitro-6-(trifluoromethyl)aniline have shown that it degrades relatively quickly under natural conditions, reducing its potential for long-term environmental accumulation. However, proper handling and disposal practices are still essential to minimize any adverse effects on ecosystems.
In conclusion, 2-Nitro-6-(trifluoromethyl)aniline (CAS No. 24821-17-8) is a multifaceted compound with significant potential in various scientific and industrial applications. Its unique chemical structure and properties make it a valuable intermediate in pharmaceutical synthesis, materials science, and other fields. Ongoing research continues to uncover new uses and improvements for this compound, highlighting its importance in modern chemistry.
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