Cas no 28447-17-8 (Ethyl (E)-3-(3-Pyridinyl)-2-propenoate)
Ethyl (E)-3-(3-Pyridinyl)-2-propenoate Chemical and Physical Properties
Names and Identifiers
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- Ethyl 3-(pyridin-3-yl)acrylate
- (E)-ethyl 3-(pyridin-3-yl)acrylate
- 3-PYRIDINEACRYLIC ACID ETHYL ESTER
- ETHYL 3-(3-PYRIDYL)ACRYLATE
- Ethyl 3-(3-pyridyl)propenoate
- 3PYAAE
- 3-pyridin-3-yl-acrylic acid ethyl ester
- AURORA KA-1039
- Ethyl 3-pyridineacrylate
- RARECHEM AL BI 1522
- ethyl (E)-3-(3-pyridinyl)-2-propenoate
- ethyl (E)-3-pyridin-3-ylprop-2-enoate
- W-203225
- 59607-99-7
- CE-0210
- SCHEMBL533790
- J-502030
- ethyl trans-3-(3-pyridyl)acrylate
- Ethyl (2E)-3-(3-pyridinyl)-2-propenoate #
- DTXSID50905036
- EN300-1455928
- (E)-ethyl3-(pyridin-3-yl)acrylate
- W11611
- 28447-17-8
- ethyl (2E)-3-(pyridin-3-yl)prop-2-enoate
- CHEMBL2289662
- A853261
- Ethyl-3-pyridine acrylate
- CS-0088304
- AKOS005072199
- MFCD02177443
- 2-Propenoic acid, 3-(3-pyridinyl)-, ethyl ester, (E)-
- 3-Pyridin-3-ylacrylic Acid Ethyl Ester;
- ALBB-032764
- Ethyl (E)-3-(3-Pyridinyl)-2-propenoate
-
- Inchi: 1S/C10H11NO2/c1-2-13-10(12)6-5-9-4-3-7-11-8-9/h3-8H,2H2,1H3/b6-5+
- InChI Key: PIEQSBWGIODYPE-AATRIKPKSA-N
- SMILES: O(C(/C=C/C1C=NC=CC=1)=O)CC
Computed Properties
- Exact Mass: 177.07900
- Monoisotopic Mass: 177.079
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 13
- Rotatable Bond Count: 4
- Complexity: 189
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 1
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 39.2A^2
- XLogP3: 1.5
Experimental Properties
- Density: 1.1±0.1 g/cm3
- Melting Point: NA
- Boiling Point: 285.2±15.0 °C at 760 mmHg
- Flash Point: Not available
- Refractive Index: 1.553
- PSA: 39.19000
- LogP: 1.65790
- Vapor Pressure: 0.0±0.6 mmHg at 25°C
Ethyl (E)-3-(3-Pyridinyl)-2-propenoate Security Information
- Signal Word:warning
- Hazard Statement: H303May be harmful if swallowed+H313Skin contact may be harmful+H333Inhalation may be harmful to the body
-
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 - Safety Instruction: H303May be harmful if swallowed+H313Skin contact may be harmful+H333Inhalation may be harmful to the body
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
Ethyl (E)-3-(3-Pyridinyl)-2-propenoate Customs Data
- HS CODE:2933399090
- Customs Data:
China Customs Code:
2933399090Overview:
2933399090. Other compounds with non fused pyridine rings in structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date
Summary:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Ethyl (E)-3-(3-Pyridinyl)-2-propenoate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM374529-1g |
Ethyl 3-(pyridin-3-yl)acrylate |
28447-17-8 | 95%+ | 1g |
$117 | 2022-06-11 | |
| Chemenu | CM374529-5g |
Ethyl 3-(pyridin-3-yl)acrylate |
28447-17-8 | 95%+ | 5g |
$367 | 2022-06-11 | |
| Apollo Scientific | OR303585-500mg |
Ethyl (E)-3-(3-pyridinyl)-2-propenoate |
28447-17-8 | 500mg |
£70.00 | 2023-08-31 | ||
| Apollo Scientific | OR303585-1g |
Ethyl (E)-3-(3-pyridinyl)-2-propenoate |
28447-17-8 | 1g |
£90.00 | 2023-08-31 | ||
| Apollo Scientific | OR303585-5g |
Ethyl (E)-3-(3-pyridinyl)-2-propenoate |
28447-17-8 | 5g |
£161.00 | 2025-02-19 | ||
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X91445-1g |
ethyl 3-(pyridin-3-yl)acrylate |
28447-17-8 | 99% | 1g |
¥648.0 | 2023-09-05 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X91445-5g |
ethyl 3-(pyridin-3-yl)acrylate |
28447-17-8 | 99% | 5g |
¥2088.0 | 2023-09-05 | |
| TRC | E927620-5mg |
Ethyl (E)-3-(3-Pyridinyl)-2-propenoate |
28447-17-8 | 5mg |
$ 50.00 | 2022-06-05 | ||
| TRC | E927620-10mg |
Ethyl (E)-3-(3-Pyridinyl)-2-propenoate |
28447-17-8 | 10mg |
$ 65.00 | 2022-06-05 | ||
| TRC | E927620-50mg |
Ethyl (E)-3-(3-Pyridinyl)-2-propenoate |
28447-17-8 | 50mg |
$ 80.00 | 2022-06-05 |
Ethyl (E)-3-(3-Pyridinyl)-2-propenoate Suppliers
Ethyl (E)-3-(3-Pyridinyl)-2-propenoate Related Literature
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1. An investigation of the electrochemical delithiation process of carbon coated α-Fe2O3nanoparticlesAdrian Brandt,Florian Winter,Sebastian Klamor,Frank Berkemeier,Jatinkumar Rana,Rainer P?ttgen,Andrea Balducci J. Mater. Chem. A, 2013,1, 11229-11236
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Sandip Gangadhar Balwe,Yeon Tae Jeong Org. Biomol. Chem., 2018,16, 1287-1296
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Christian K. Rank,Alexander W. Jones,Tatjana Wall,Patrick Di Martino-Fumo,Sarah Schr?ck,Markus Gerhards,Frederic W. Patureau Chem. Commun., 2019,55, 13749-13752
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Benjamin Gabriel Poulson,Kacper Szczepski,Joanna Izabela Lachowicz,Lukasz Jaremko,Abdul-Hamid Emwas,Mariusz Jaremko RSC Adv., 2020,10, 215-227
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Alvin Tanudjaja,Shinsuke Inagi,Fusao Kitamura,Toshikazu Takata,Ikuyoshi Tomita Dalton Trans., 2021,50, 3037-3043
Additional information on Ethyl (E)-3-(3-Pyridinyl)-2-propenoate
Comprehensive Overview of Ethyl (E)-3-(3-Pyridinyl)-2-propenoate (CAS No. 28447-17-8)
Ethyl (E)-3-(3-Pyridinyl)-2-propenoate, with the CAS number 28447-17-8, is a versatile organic compound widely utilized in pharmaceutical and agrochemical research. This ester derivative, featuring a pyridine ring and an (E)-configured propenoate moiety, has garnered significant attention due to its potential applications in drug discovery and material science. Its molecular structure combines the aromatic properties of 3-pyridinyl with the reactivity of an α,β-unsaturated ester, making it a valuable intermediate for synthesizing bioactive molecules.
In recent years, the demand for pyridine-based compounds like Ethyl (E)-3-(3-Pyridinyl)-2-propenoate has surged, driven by their role in developing kinase inhibitors and antimicrobial agents. Researchers frequently search for "synthesis of Ethyl (E)-3-(3-Pyridinyl)-2-propenoate" or "applications of CAS 28447-17-8," reflecting its relevance in modern chemistry. The compound’s Michael acceptor capability also positions it as a key player in click chemistry and polymer cross-linking reactions, aligning with trends in sustainable material design.
From an analytical perspective, 28447-17-8 exhibits distinct spectroscopic signatures, including characteristic IR carbonyl stretches (~1700 cm?1) and NMR chemical shifts for the pyridine protons (δ 8.5–9.0 ppm). These features facilitate its identification in complex mixtures, a topic often queried as "spectral data of Ethyl (E)-3-(3-Pyridinyl)-2-propenoate." Additionally, its stability under ambient conditions and solubility in common organic solvents (e.g., DMSO, ethanol) enhance its practicality in lab settings.
The compound’s mechanism of action in biological systems often revolves around its ability to form covalent bonds with nucleophilic residues, a property exploited in "proteomics research" and "targeted drug delivery." Recent publications highlight its utility in designing fluorescent probes for cellular imaging, addressing the growing interest in "bioimaging reagents" among life scientists. Regulatory databases confirm its non-hazardous status for standard handling, though proper lab protocols are always recommended.
Innovations in green chemistry have further spotlighted Ethyl (E)-3-(3-Pyridinyl)-2-propenoate as a candidate for solvent-free reactions. Queries like "eco-friendly synthesis of pyridine esters" underscore this trend. Its compatibility with microwave-assisted and flow chemistry techniques also aligns with industrial demands for scalable, energy-efficient processes. As research continues, this compound’s role in heterocyclic chemistry and medicinal chemistry is expected to expand, solidifying its position as a cornerstone in synthetic methodologies.
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