Cas no 623-17-6 (Furfuryl acetate)
Furfuryl acetate Chemical and Physical Properties
Names and Identifiers
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- Furan-2-ylmethyl acetate
- 2-acetoxymethylfuran
- 2-furanmethanol acetate
- 2-Furylcarbinyl acetate
- Furfuryl Acetate
- FURFURYL ACETATE(AS)
- Acetic Acid Furfuryl Ester
- 2-Furanmethanol, acetate
- Furfuryl alcohol, acetate
- 2-Furfuryl acetate
- Acetic acid furfurylester
- 2-Furylmethyl acetate
- 2-Furanmethyl acetate
- 2-Furanmethanol, 2-acetate
- 2-Furfuryl-acetate
- FEMA No. 2490
- 3CJC9ALG3X
- DSSTox_CID_5346
- DSSTox_RID_77759
- DSSTox_GSID_25346
- Fur
- Furfuryl acetate
-
- MDL： MFCD00003251
- Inchi： 1S/C7H8O3/c1-6(8)10-5-7-3-2-4-9-7/h2-4H,5H2,1H3
- InChI Key： CKOYRRWBOKMNRG-UHFFFAOYSA-N
- SMILES： O1C([H])=C([H])C([H])=C1C([H])([H])OC(C([H])([H])[H])=O
- BRN： 0116128
Computed Properties
- Exact Mass: 140.04700
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 10
- Rotatable Bond Count: 3
- Complexity: 122
- 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: 0.7
- Topological Polar Surface Area: 39.4
Experimental Properties
- Color/Form: Yellow liquid. It has fruity, medicinal and pungent fragrance.
- Density: 1.118?g/mL?at 25?°C(lit.)
- Boiling Point: 175-177?°C(lit.)
- Flash Point: Fahrenheit: 150.8 ° f < br / > Celsius: 66 ° C < br / >
- Refractive Index: n20/D 1.462(lit.)
- Water Partition Coefficient: 0.5-1.0 g/100 mL at 23 oC
- PSA: 39.44000
- LogP: 1.34270
- Solubility: It is soluble in alcohol and ether, insoluble in water, and turns brown when exposed to light in air.
- FEMA: 2490
Furfuryl acetate Security Information
- Prompt：warning
- Signal Word：Warning
- Hazard Statement： H227
- Warning Statement： P210-P280-P403+P235-P501
- WGK Germany：3
- Hazard Category Code： 36/37/38
- Safety Instruction： S24/25-S37/39-S26
- RTECS：LU9120000
-
Hazardous Material Identification：
- Risk Phrases：R36/37/38
- Safety Term：S24/25
- TSCA：Yes
- Storage Condition：Store at room temperature
Furfuryl acetate Customs Data
- HS CODE：2932190090
- Customs Data：
China Customs Code:
2932190090Overview:
2932190090 Other structurally non fused furan ring compounds. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:20.0%
Declaration elements:
Product Name, component content, use to
Summary:
2932190090 other compounds containing an unfused furan ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%
Furfuryl acetate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | A0903-25ml |
Furfuryl acetate |
623-17-6 | 97.0%(GC) | 25ml |
￥190.0 | 2022-05-30 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | F158A-25g |
Furfuryl acetate |
623-17-6 | 98% | 25g |
￥39.0 | 2022-05-30 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | F158A-100g |
Furfuryl acetate |
623-17-6 | 98% | 100g |
￥138.0 | 2022-05-30 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | F158A-500g |
Furfuryl acetate |
623-17-6 | 98% | 500g |
￥427.0 | 2022-05-30 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | A0903-100ml |
Furfuryl acetate |
623-17-6 | 97.0%(GC) | 100ml |
￥750.0 | 2022-05-30 | |
| Fluorochem | 068583-10g |
Furfuryl acetate |
623-17-6 | 97% | 10g |
￡10.00 | 2022-03-01 | |
| Fluorochem | 068583-25g |
Furfuryl acetate |
623-17-6 | 97% | 25g |
￡17.00 | 2022-03-01 | |
| Fluorochem | 068583-500g |
Furfuryl acetate |
623-17-6 | 97% | 500g |
￡49.00 | 2022-03-01 | |
| NAN JING HUA XUE SHI JI GU FEN Co., Ltd. | C0831850043- 25g |
Furfuryl acetate |
623-17-6 | 97.0% | 25g |
￥ 34.1 | 2021-05-18 | |
| NAN JING HUA XUE SHI JI GU FEN Co., Ltd. | C0831850035- 100g |
Furfuryl acetate |
623-17-6 | 97.0% | 100g |
￥ 108.2 | 2021-05-18 |
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Furfuryl acetate Related Literature
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M. Pilar Delgado de la Torre,Feliciano Priego-Capote,María Dolores Luque de Castro Anal. Methods 2015 7 1758
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2. Role of lattice strain in bifunctional catalysts for tandem furfural hydrogenation–esterificationLuqman H. Hashim,Ahmed Halilu,Yahaya Balarabe Umar,Mohd Rafie Bin Johan,Mohamed Kheireddine Aroua,Paramita Koley,Suresh K. Bhargava Catal. Sci. Technol. 2023 13 774
Related Categories
- Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Heteroaromatic compounds Heteroaromatic compounds
- Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Heteroaromatic compounds
- Solvents and Organic Chemicals Organic Compounds Heterocyclic Compounds
Additional information on Furfuryl acetate
Furfuryl acetate (CAS No. 623-17-6): Chemical Profile and Emerging Applications
Furfuryl acetate, with the chemical formula C7H8O2 and CAS number 623-17-6, is an ester derivative that has garnered significant attention in the chemical and pharmaceutical industries due to its versatile reactivity and broad spectrum of applications. This compound, also known as 2-furoyl acetate, is a clear, colorless liquid with a characteristic fruity odor, making it a valuable intermediate in organic synthesis and industrial processes.
The structural integrity of furfuryl acetate features a furfuryl group (C5H4O) attached to an acetyl moiety (CH3COO-). This unique configuration imparts distinct chemical properties that make it highly useful in various synthetic pathways. The compound's ability to participate in nucleophilic addition reactions, condensation reactions, and hydrogenation processes underscores its importance in the synthesis of more complex molecules.
In recent years, furfuryl acetate has found increasing relevance in the field of medicinal chemistry. Its role as a precursor in the synthesis of pharmacologically active compounds has been extensively studied. For instance, researchers have explored its utility in the preparation of nonsteroidal anti-inflammatory drugs (NSAIDs) and other therapeutic agents. The ester group in furfuryl acetate allows for facile modifications, enabling chemists to tailor molecular structures for enhanced biological activity.
A notable application of furfuryl acetate lies in its use as a solvent and reagent in polymer chemistry. Its ability to dissolve a wide range of polymers makes it a preferred choice for formulating resins and coatings. Additionally, the compound's compatibility with other monomers and additives enhances its utility in producing high-performance materials with specific mechanical and thermal properties.
The agrochemical sector has also recognized the potential of furfuryl acetate. It serves as an intermediate in the synthesis of herbicides and fungicides, contributing to the development of more effective crop protection agents. The compound's stability under various environmental conditions ensures consistent performance in agricultural applications.
Recent advancements in green chemistry have prompted investigations into sustainable methods for producing furfuryl acetate. Researchers are exploring biocatalytic routes that minimize waste and energy consumption. These efforts align with global initiatives to promote environmentally friendly chemical processes, ensuring that the demand for this compound can be met responsibly.
The pharmaceutical industry continues to leverage furfuryl acetate for its role in drug discovery and development. Its incorporation into novel molecular frameworks has led to the identification of promising candidates for treating neurological disorders, infectious diseases, and metabolic conditions. The compound's versatility as a synthetic building block remains a cornerstone in medicinal chemistry innovation.
In conclusion, furfuryl acetate (CAS No. 623-17-6) is a multifaceted compound with far-reaching applications across multiple industries. Its unique chemical properties make it indispensable in organic synthesis, polymer production, agrochemical formulations, and pharmaceutical research. As scientific understanding evolves, the potential uses for this compound are expected to expand further, driven by ongoing research and technological advancements.
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