Cas no 1075-49-6 (4-Vinylbenzoic acid)
4-Vinylbenzoic acid Chemical and Physical Properties
Names and Identifiers
-
- 4-Vinylbenzoic acid
- 4-ethenyl-benzoic acid
- Styrene-4-carboxylic acid
- 4-Vinylbenzoic Acid (stabilized with BHT)
- 4-ethenylBenzoic acid
- p-Vinylbenzoic Acid
- 4-Carboxystyrene
- 4-Carboxystyrene (stabilized with BHT)
- NSC 176003
- p-Carboxystyrene
- 4-ethenylbenzoate
- VINYLBENZOIC ACID
- TIMTEC-BB SBB006579
- RARECHEM AL BO 0691
- 4-VinylbenzoicAcid99%
- Benzoic acid, 4-ethenyl-
- 4-VinYl-Benzoic Acid
- TBU4QT9N3K
- IRQWEODKXLDORP-UHFFFAOYSA-N
- p-vinyl benzoic acid
- 4-vinyl benzoic acid
- para-vinyl benzoic acid
- PubChem12624
- KSC181O7H
- IRQWEODKXLDO
- IRQWEODKXLDORP-UHFFFAOYSA-
- AM20020177
- NSC-176003
- 4-Vinylbenzoic acid, 97%
- 4-vinylbenzoate
- EN300-106706
- SY011290
- EINECS 214-053-4
- GEO-03384
- J-516028
- MFCD00002569
- FT-0619550
- Q2403334
- MW7
- V0059
- NSC176003
- DTXSID70148069
- 4-Vinylbenzoic Acid, (stabilized with BHT)
- AKOS006222563
- BENZOIC ACID, P-VINYL-
- CS-W007654
- PS-5895
- NS00023466
- 1075-49-6
- UNII-TBU4QT9N3K
- AC-33572
- A801723
- 28391-39-1
- SCHEMBL13341634
- InChI=1/C9H8O2/c1-2-7-3-5-8(6-4-7)9(10)11/h2-6H,1H2,(H,10,11)
- SCHEMBL16536
- 4-VINYLBENZOICACID
- DB-040767
-
- MDL: MFCD00002569
- Inchi: 1S/C9H8O2/c1-2-7-3-5-8(6-4-7)9(10)11/h2-6H,1H2,(H,10,11)
- InChI Key: IRQWEODKXLDORP-UHFFFAOYSA-N
- SMILES: OC(C1C=CC(C=C)=CC=1)=O
- BRN: 2041130
Computed Properties
- Exact Mass: 148.05200
- Monoisotopic Mass: 148.05243
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 11
- Rotatable Bond Count: 2
- Complexity: 155
- 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
- Molecular Weight: 148.16
- Surface Charge: 0
- XLogP3: 2.7
- Topological Polar Surface Area: 37.3
Experimental Properties
- Color/Form: Off white to beige powder.
- Density: 1.3
- Melting Point: 142-144?°C (lit.)
- Boiling Point: 228.74°C (rough estimate)
- Flash Point: 132.8℃
- Refractive Index: 1.5290 (estimate)
- Solubility: Soluble in dichloromethane and methanol
- Stability/Shelf Life: Store in a Cool Dry Area.
- PSA: 37.30000
- LogP: 2.02780
- Sensitiveness: Light Sensitive
- Solubility: Not determined
4-Vinylbenzoic 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-S36-S37/39
- FLUKA BRAND F CODES:10
-
Hazardous Material Identification:
- Safety Term:S26;S37/39
- Risk Phrases:R36/37/38
- HazardClass:IRRITANT, KEEP COLD
- Storage Condition:0-10°C
4-Vinylbenzoic acid Customs Data
- HS CODE:2916399090
- Customs Data:
China Customs Code:
2916399090Overview:
2916399090 Other aromatic monocarboxylic acids. 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, Acrylic acid\Acrylates or esters shall be packaged clearly
Summary:
2916399090 other aromatic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%
4-Vinylbenzoic acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | 001222-1g |
4-Vinylbenzoic acid |
1075-49-6 | 97% | 1g |
£17.00 | 2022-03-29 | |
| Fluorochem | 001222-5g |
4-Vinylbenzoic acid |
1075-49-6 | 97% | 5g |
£60.00 | 2022-03-29 | |
| Fluorochem | 001222-10g |
4-Vinylbenzoic acid |
1075-49-6 | 97% | 10g |
£90.00 | 2022-03-29 | |
| Fluorochem | 001222-25g |
4-Vinylbenzoic acid |
1075-49-6 | 97% | 25g |
£142.00 | 2022-03-29 | |
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 254738-1G |
4-Vinylbenzoic acid |
1075-49-6 | 1g |
¥582.97 | 2023-12-09 | ||
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 254738-5G |
4-Vinylbenzoic acid |
1075-49-6 | 5g |
¥2817.87 | 2023-12-09 | ||
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | V0059-25G |
4-Vinylbenzoic Acid (stabilized with BHT) |
1075-49-6 | >97.0%(GC)(T) | 25g |
¥1990.00 | 2024-04-18 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | V117230-1g |
4-Vinylbenzoic acid |
1075-49-6 | 97%,100ppm BHT | 1g |
¥75.90 | 2023-08-31 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | V117230-100g |
4-Vinylbenzoic acid |
1075-49-6 | 97%,100ppm BHT | 100g |
¥2182.90 | 2023-08-31 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | V117230-25g |
4-Vinylbenzoic acid |
1075-49-6 | 97%,100ppm BHT | 25g |
¥840.90 | 2023-08-31 |
4-Vinylbenzoic acid Suppliers
4-Vinylbenzoic acid Related Literature
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Saloni Mehra,Safiya Nisar,Sonal Chauhan,Gurmeet Singh,Virender Singh,Sunita Rattan Polym. Chem. 2021 12 2404
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D. Gr?fe,S. Zschoche,D. Appelhans,B. Voit RSC Adv. 2016 6 34809
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Related Categories
- Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzoic acids
- Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzoic acids and derivatives Benzoic acids
- Solvents and Organic Chemicals Organic Compounds Acids/Esters
- Pharmaceutical and Biochemical Products Pharmaceutical Intermediates
Additional information on 4-Vinylbenzoic acid
Introduction to 4-Vinylbenzoic Acid (CAS No. 1075-49-6)
4-Vinylbenzoic acid, with the chemical formula C?H?O? and CAS number 1075-49-6, is a versatile organic compound that has garnered significant attention in the field of pharmaceuticals, agrochemicals, and material science. This compound serves as a crucial intermediate in the synthesis of various functional materials and bioactive molecules, making it a subject of extensive research and industrial application.
The unique structure of 4-vinylbenzoic acid features a benzoic acid moiety attached to a vinyl group at the para position. This configuration imparts reactivity that is highly valuable for polymerization processes, cross-linking reactions, and the development of novel drug candidates. The presence of both an aromatic ring and a reactive double bond allows for diverse chemical modifications, enabling its use in synthesizing complex molecules with tailored properties.
In recent years, 4-vinylbenzoic acid has been extensively studied for its potential applications in medicinal chemistry. Researchers have leveraged its reactivity to develop new therapeutic agents targeting various diseases. For instance, studies have demonstrated its role in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs) and other pharmacologically active compounds. The compound’s ability to undergo Michael addition reactions makes it particularly useful in constructing heterocyclic frameworks, which are prevalent in many bioactive molecules.
Moreover, 4-vinylbenzoic acid has found utility in the field of advanced materials. Its incorporation into polymer matrices enhances the mechanical and thermal properties of synthetic resins, making it valuable for applications in coatings, adhesives, and composite materials. The vinyl group’s capability to participate in radical polymerization reactions allows for the creation of high-performance polymers with specific functionalities.
Recent advancements in green chemistry have also highlighted the importance of 4-vinylbenzoic acid as a sustainable building block. Researchers are exploring methods to produce this compound using environmentally friendly processes, such as catalytic hydrogenation and biocatalytic routes. These efforts align with the growing demand for eco-conscious chemical synthesis methods across industries.
The pharmaceutical industry has been particularly keen on exploring the therapeutic potential of derivatives of 4-vinylbenzoic acid. For example, researchers have synthesized analogs that exhibit antimicrobial and antiviral properties. These derivatives are being tested in preclinical studies to evaluate their efficacy against various pathogens. The benzoic acid moiety is known for its pharmacological activity, which can be modulated by introducing different substituents at strategic positions on the aromatic ring.
In material science, 4-vinylbenzoic acid has been utilized to develop photoactive materials for organic electronics. Its ability to absorb light across multiple wavelengths makes it suitable for use in photovoltaic cells and optoelectronic devices. Additionally, its incorporation into liquid crystals enhances their stability and performance, contributing to advancements in display technologies.
The synthesis of 4-vinylbenzoic acid typically involves the vinylation of benzoic acid or its derivatives using traditional organic chemistry techniques. However, modern synthetic methodologies are focusing on more efficient and scalable processes. For instance, transition metal-catalyzed cross-coupling reactions have been employed to introduce the vinyl group with high selectivity and yield. These innovations are streamlining the production of 4-vinylbenzoic acid, making it more accessible for industrial applications.
Industrial applications of 4-vinylbenzoic acid extend beyond pharmaceuticals and materials science. It is widely used as a monomer in producing specialty polymers that exhibit unique properties such as UV resistance and chemical stability. These polymers find applications in automotive components, aerospace materials, and medical implants where durability is paramount.
Recent research has also explored the role of 4-vinylbenzoic acid in drug delivery systems. Its ability to form stable complexes with other molecules has been exploited to develop controlled-release formulations. These systems enhance drug bioavailability while minimizing side effects, representing a significant advancement in therapeutic strategies.
The future prospects for 4-vinylbenzoic acid appear promising as researchers continue to uncover new applications and refine synthetic methodologies. Its versatility makes it a valuable compound for interdisciplinary research, bridging gaps between chemistry, biology, and engineering. As innovation continues at a rapid pace, 4-vinylbenzoic acid is poised to remain a cornerstone material in both academic research and industrial development.
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