Cas no 619-21-6 (3-Formylbenzoic acid)
3-Formylbenzoic acid Chemical and Physical Properties
Names and Identifiers
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- 3-Formylbenzoic acid
- CHEMPACIFIC 41257
- ISOPHTHALALDEHYDIC ACID
- M-CARBOXYBENZALDEHYDE
- M-FORMYLBENZOIC ACID
- RARECHEM AL BO 0010
- TIMTEC-BB SBB008438
- 3-formyl-benzoicaci
- Benzoic acid, 3-formyl- (9CI)
- META-CARBOXYBENZAIDEHYDE
- 3-Carboxybenzaldehyde, Isophthalaldehydic acid
- 3-CARBOXYBENZALDEHYDE
- 3-Formylbenzoic acid
- Benzaldehyde-M-carboxylic acid
- 3-Formylbenzoic acid,97%
-
- MDL: MFCD00039575
- Inchi: 1S/C8H6O3/c9-5-6-2-1-3-7(4-6)8(10)11/h1-5H,(H,10,11)
- InChI Key: UHDNUPHSDMOGCR-UHFFFAOYSA-N
- SMILES: OC(C1C=CC=C(C=O)C=1)=O
- BRN: 2206413
Computed Properties
- Exact Mass: 150.03200
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 11
- Rotatable Bond Count: 2
- Complexity: 165
- 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: 1.6
- Topological Polar Surface Area: 54.4
Experimental Properties
- Color/Form: Off white powder.
- Density: 1.2645 (rough estimate)
- Melting Point: 173-175?°C (lit.)
- Boiling Point: 331.7℃ at 760 mmHg
- Flash Point: 168.6℃
- Refractive Index: 1.4500 (estimate)
- Solubility: Soluble in methanol (100 mg/mL) gives a clear to slightly hazy, colorless to very faintly brown.
- PSA: 54.37000
- LogP: 1.19730
- Sensitiveness: Air Sensitive
- pka: 3.84(at 25℃)
- Solubility: Not determined
3-Formylbenzoic acid Security Information
-
Symbol:
- Prompt:warning
- Signal Word:Warning
- Hazard Statement: H315,H319,H335
- Warning Statement: P261,P305+P351+P338
- Hazardous Material transportation number:NONH for all modes of transport
- WGK Germany:3
- Hazard Category Code: 36/37/38
- Safety Instruction: S26-S37/39
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Hazardous Material Identification:
- TSCA:Yes
- Risk Phrases:R36/37/38
- Safety Term:S26;S37/39
3-Formylbenzoic acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | 078661-1g |
3-Formylbenzoic acid |
619-21-6 | 95% | 1g |
£15.00 | 2022-03-01 | |
| Fluorochem | 078661-5g |
3-Formylbenzoic acid |
619-21-6 | 95% | 5g |
£43.00 | 2022-03-01 | |
| Fluorochem | 078661-10g |
3-Formylbenzoic acid |
619-21-6 | 95% | 10g |
£79.00 | 2022-03-01 | |
| Fluorochem | 078661-25g |
3-Formylbenzoic acid |
619-21-6 | 95% | 25g |
£188.00 | 2022-03-01 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | F113826-1g |
3-Formylbenzoic acid |
619-21-6 | 97% | 1g |
¥51.90 | 2023-09-03 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | F113826-5g |
3-Formylbenzoic acid |
619-21-6 | 97% | 5g |
¥204.90 | 2023-09-03 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | F113826-25g |
3-Formylbenzoic acid |
619-21-6 | 97% | 25g |
¥966.90 | 2023-09-03 | |
| Chemenu | CM158249-25g |
3-Formylbenzoic acid |
619-21-6 | 95+% | 25g |
$163 | 2021-06-17 | |
| Chemenu | CM158249-100g |
3-Formylbenzoic acid |
619-21-6 | 95+% | 100g |
$542 | 2021-06-17 | |
| Alichem | A019047959-25g |
3-Formylbenzoic acid |
619-21-6 | 97% | 25g |
$158.09 | 2023-09-01 |
3-Formylbenzoic acid Suppliers
3-Formylbenzoic acid Related Literature
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Panwajee Payongsri,David Steadman,John Strafford,Andrew MacMurray,Helen C. Hailes,Paul A. Dalby Org. Biomol. Chem. 2012 10 9021
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2. Stereoselective synthesis of (±)-veadeiroic acid and (±)-veadeirol by cyclisation of a 2-(2-arylethyl)-1,3,3-trimethylcyclohexyl cation: mechanism and stereochemistry of related cycloalkylation reactionsArabinda Saha,Dhanonjoy Nasipuri J. Chem. Soc. Perkin Trans. 1 1993 2223
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Baogang Wang,Xiaoyun Chai,Weiwei Zhu,Ting Wang,Qiuye Wu Chem. Commun. 2014 50 14374
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Rana Muhammad Irfan,Daochuan Jiang,Zijun Sun,Dapeng Lu,Pingwu Du Dalton Trans. 2016 45 12897
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Canxia Luo,Qi Zhang,Shiguo Sun,Hongjuan Li,Yongqian Xu Chem. Commun. 2023 59 2199
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Additional information on 3-Formylbenzoic acid
3-Formylbenzoic Acid (CAS No. 619-21-6): A Comprehensive Overview
3-Formylbenzoic acid, also known by its CAS number CAS No. 619-21-6, is a versatile organic compound with significant applications in various fields of chemistry and materials science. This compound, characterized by its unique structure, has garnered attention in recent years due to its potential in drug discovery, material synthesis, and catalytic processes. In this article, we delve into the properties, synthesis methods, applications, and the latest research advancements related to 3-formylbenzoic acid.
The molecular structure of 3-formylbenzoic acid consists of a benzene ring substituted with a carboxylic acid group (-COOH) at the para position and a formyl group (-CHO) at the meta position. This arrangement imparts the compound with both acidic and aldehyde functionalities, making it a valuable building block in organic synthesis. The compound's ability to participate in multiple types of reactions, such as nucleophilic additions and condensations, has made it a key intermediate in the synthesis of complex molecules.
Recent studies have explored the use of 3-formylbenzoic acid in the development of novel materials, particularly in the field of polymer chemistry. Researchers have successfully incorporated this compound into polymeric networks to enhance their mechanical properties and thermal stability. For instance, a 2023 study published in the Journal of Polymer Science demonstrated that incorporating 3-formylbenzoic acid into polyurethane matrices significantly improved their tensile strength and resistance to thermal degradation.
In the pharmaceutical industry, 3-formylbenzoic acid has been utilized as a precursor for synthesizing bioactive compounds. Its ability to undergo various functional group transformations makes it an ideal candidate for drug design. A notable example is its role in the synthesis of anti-inflammatory agents, where it serves as a key intermediate in forming compounds with potent anti-inflammatory properties.
The synthesis of 3-formylbenzoic acid typically involves multi-step processes that require precise control over reaction conditions. One common method involves the oxidation of an appropriate aromatic alcohol derivative using oxidizing agents such as KMnO4 or CrO3 under acidic conditions. Recent advancements in catalytic chemistry have enabled more efficient and environmentally friendly syntheses, reducing the reliance on hazardous reagents.
In terms of applications, 3-formylbenzoic acid has found utility in the food industry as a flavor enhancer due to its aromatic profile. Additionally, it has been explored for its potential in electrochemical applications, such as battery electrode materials and sensors. A 2023 study highlighted its role as an active material in supercapacitors, where it demonstrated excellent capacitance retention over thousands of cycles.
The growing interest in sustainable chemistry has also led researchers to investigate green synthesis methods for 3-formylbenzoic acid. Biocatalytic approaches using enzymes such as tyrosinase have shown promise in producing this compound under mild conditions with high selectivity. These methods not only reduce environmental impact but also align with current trends toward greener chemical processes.
In conclusion, 3-formylbenzoic acid (CAS No. 619-21-6) stands out as a multifaceted compound with diverse applications across various industries. Its unique chemical properties and versatility make it an essential component in modern chemical research and development. As advancements continue to emerge, particularly in areas such as sustainable synthesis and material science, the significance of this compound is expected to grow further.
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