Cas no 1878-87-1 (2-(2-nitrophenoxy)acetic acid)
2-(2-nitrophenoxy)acetic acid Chemical and Physical Properties
Names and Identifiers
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- 2-Nitrophenoxyacetic acid
- 2-(2-Nitrophenoxy)acetic acid
- o-Nitrophenoxyacetic Acid
- (2-Nitro-phenoxy)-essigsaeure
- 2-Nitro-phenylaetherglykolsaeure
- F0020-1820
- O-(2-Nitro-phenyl)-glykolsaeure
- TIMTEC-BB SBB000361
- 2-(2-nitrophenoxy)ethanoic acid
- 254
- AKOS BBB
- AKOS BBB/254
- AKOS BBS-00007711
- 2-NITROPHENOXYACETIC ACID, 98+%
- (2-Nitrophenoxy)acetic acid
- Acetic acid, (2-nitrophenoxy)-
- o-nitrophenoxy acetic acid
- TYHHDWAHJRRYCU-UHFFFAOYSA-N
- 2-NitrophenoxyaceticAcid
- (O-Nitrophenoxy)acetic acid
- Oprea1_748771
- ARONIS009917
- Acetic acid,2-(2-nitrophenoxy)-
- NSC37409
- Acet
- 2-(2-nitrophenoxy)acetic acid
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- MDL: MFCD00016993
- Inchi: 1S/C8H7NO5/c10-8(11)5-14-7-4-2-1-3-6(7)9(12)13/h1-4H,5H2,(H,10,11)
- InChI Key: TYHHDWAHJRRYCU-UHFFFAOYSA-N
- SMILES: O(CC(=O)O)C1C=CC=CC=1[N+](=O)[O-]
- BRN: 2114909
Computed Properties
- Exact Mass: 197.03200
- Monoisotopic Mass: 197.032422
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 14
- Rotatable Bond Count: 3
- Complexity: 224
- 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
- XLogP3: 1
- Topological Polar Surface Area: 92.4
Experimental Properties
- Color/Form: powder
- Density: 1.5023 (rough estimate)
- Melting Point: 156.0 to 160.0 deg-C
- Boiling Point: 334.23°C (rough estimate)
- Flash Point: 188.7 °C
- Refractive Index: 1.5700 (estimate)
- Water Partition Coefficient: dissolution
- PSA: 92.35000
- LogP: 1.58140
- Solubility: Insoluble
2-(2-nitrophenoxy)acetic acid Security Information
-
Symbol:
- Prompt:warning
- Hazard Statement: H315-H319
- Warning Statement: P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
- WGK Germany:3
- Hazard Category Code: R22;R36/37/38;R44
- Safety Instruction: S22-S24/25-S37/39-S26
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Hazardous Material Identification:
- Safety Term:S26;S37/39
- Risk Phrases:R22; R36/37/38; R44
- HazardClass:IRRITANT
2-(2-nitrophenoxy)acetic acid Customs Data
- HS CODE:2918990090
- Customs Data:
China Customs Code:
2918990090Overview:
2918990090. Other additional oxy carboxylic acids(Including anhydrides\Acyl halide\Peroxides, peroxyacids and derivatives of this tax number). 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
Summary:
2918990090. other carboxylic acids with additional oxygen function and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
2-(2-nitrophenoxy)acetic acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | 160900-5g |
2-Nitrophenoxyacetic acid; >98% |
1878-87-1 | >98.0%(GC)(T) | 5g |
£13.00 | 2022-02-28 | |
| Fluorochem | 160900-25g |
2-Nitrophenoxyacetic acid; >98% |
1878-87-1 | >98.0%(GC)(T) | 25g |
£50.00 | 2022-02-28 | |
| Fluorochem | 160900-100g |
2-Nitrophenoxyacetic acid; >98% |
1878-87-1 | >98.0%(GC)(T) | 100g |
£188.00 | 2022-02-28 | |
| Fluorochem | 160900-500g |
2-Nitrophenoxyacetic acid; >98% |
1878-87-1 | >98.0%(GC)(T) | 500g |
£563.00 | 2022-02-28 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | N159458-100g |
2-(2-nitrophenoxy)acetic acid |
1878-87-1 | 98% | 100g |
¥1529.90 | 2023-09-01 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | N159458-1g |
2-(2-nitrophenoxy)acetic acid |
1878-87-1 | 98% | 1g |
¥29.90 | 2023-09-01 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | N159458-25G |
2-(2-nitrophenoxy)acetic acid |
1878-87-1 | 98% | 25g |
¥478.90 | 2023-09-01 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | N159458-5G |
2-(2-nitrophenoxy)acetic acid |
1878-87-1 | 98% | 5g |
¥117.90 | 2023-09-01 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | N55100-100g |
(2-nitrophenoxy)acetic acid |
1878-87-1 | 97% | 100g |
¥5009.0 | 2024-07-19 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | N55100-5g |
(2-nitrophenoxy)acetic acid |
1878-87-1 | 97% | 5g |
¥429.0 | 2024-07-19 |
2-(2-nitrophenoxy)acetic acid Related Literature
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1. CCCCI.—Heterocyclic compounds containing arsenic. Part II. Derivatives of 1 : 4-benzisooxazineGeorge Newbery,Montague Alexandra Phillips,Ralph William Ewart Stickings J. Chem. Soc. 1928 3051
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2. Alkylation and acylation reactions. Part II. The interaction of aryloxyacetyl chlorides with aluminium chlorideM. H. Palmer,G. J. McVie J. Chem. Soc. B 1968 745
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3. Formula index
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4. Benzopyrones. Part IV. Pyrano[1,4]benzoxazinones and some dihydrobenzoxazines: synthesis, mass, and nuclear magnetic resonance spectraG. Barker,G. P. Ellis,D. A. Wilson J. Chem. Soc. C 1971 2079
Additional information on 2-(2-nitrophenoxy)acetic acid
2-(2-Nitrophenoxy)Acetic Acid: A Comprehensive Overview
The compound with CAS No. 1878-87-1, commonly referred to as 2-(2-nitrophenoxy)acetic acid, is a significant molecule in the field of organic chemistry. This compound has garnered attention due to its unique chemical properties and diverse applications across various industries. Recent advancements in chemical synthesis and its utilization have further highlighted its importance in modern scientific research.
2-(2-Nitrophenoxy)acetic acid is a derivative of phenoxyacetic acid, where the phenoxy group is substituted with a nitro group at the para position. This substitution imparts distinct electronic and steric effects, making it a versatile compound for various chemical reactions. The molecule's structure allows for easy modification, enabling its use as an intermediate in the synthesis of more complex organic compounds.
One of the most notable applications of 2-(2-nitrophenoxy)acetic acid is in the field of plant physiology. Recent studies have demonstrated its role as a plant growth regulator, particularly in modulating auxin signaling pathways. Auxins are naturally occurring hormones that play a crucial role in plant growth and development. By mimicking auxin activity, this compound can influence root formation, shoot elongation, and overall plant morphology.
In addition to its biological applications, 2-(2-nitrophenoxy)acetic acid has found utility in industrial chemistry. It serves as an intermediate in the production of herbicides and pesticides, contributing to crop protection and yield enhancement. The compound's stability under various environmental conditions makes it an ideal candidate for agricultural applications.
Recent research has also explored the potential of 2-(2-nitrophenoxy)acetic acid in medicinal chemistry. Its ability to interact with specific protein targets has led to investigations into its role as a lead compound for drug development. For instance, studies have shown promise in anti-inflammatory and anti-cancer therapies, where the compound exhibits selective cytotoxicity against cancer cells while sparing healthy cells.
The synthesis of 2-(2-nitrophenoxy)acetic acid involves a multi-step process that typically begins with nitration of phenoxyacetic acid derivatives. Modern techniques have optimized this process, incorporating green chemistry principles to minimize environmental impact. These advancements have not only improved yield but also reduced production costs, making the compound more accessible for large-scale applications.
From an environmental standpoint, understanding the degradation pathways of 2-(2-nitrophenoxy)acetic acid is crucial for assessing its ecological impact. Recent studies utilizing advanced spectroscopic techniques have provided insights into its biodegradation mechanisms under aerobic and anaerobic conditions. These findings are essential for ensuring sustainable use and minimizing ecological risks associated with its application.
In conclusion, 2-(2-nitrophenoxy)acetic acid (CAS No. 1878-87-1) stands out as a versatile compound with wide-ranging applications in agriculture, industry, and medicine. Its unique chemical properties and recent research breakthroughs underscore its significance in contemporary scientific endeavors. As ongoing studies continue to uncover new potentials, this compound is poised to play an even greater role in shaping future innovations across multiple disciplines.
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