- Photoredox-catalyzed oxo-amination of aryl cyclopropanesGe, Liang; Wang, Ding-Xing; Xing, Renyi; Ma, Di; Walsh, Patrick J. ; et al, Nature Communications (2019, 2019, 10(1), 1-9
Cas no 98017-60-8 (ethyl 2-(4-methoxyphenyl)cyclopropane-1-carboxylate)
98017-60-8 structure
Product Name:ethyl 2-(4-methoxyphenyl)cyclopropane-1-carboxylate
CAS No:98017-60-8
MF:C13H16O3
MW:220.264344215393
MDL:MFCD02258631
CID:1002335
PubChem ID:244562
Update Time:2024-12-09
ethyl 2-(4-methoxyphenyl)cyclopropane-1-carboxylate Chemical and Physical Properties
Names and Identifiers
-
- ETHYL 2-(4'-METHOXYPHENYL)-1-CYCLOPROPANECARBOXYLATE
- ETHYL 2-(4-METHOXYPHENYL)CYCLOPROPANECARBOXYLATE
- Cyclopropanecarboxylic acid, 2-(p-methoxyphenyl)-, ethyl ester (6CI, 7CI)
- Ethyl 2-(4-methoxyphenyl)cyclopropane-1-carboxylate
- 345905-97-7
- Cyclopropanecarboxylic acid, 2-(4-methoxyphenyl)-, ethyl ester
- DB-416178
- EN300-130250
- SCHEMBL435326
- MFCD29925663
- Ethyl-2-(4-methoxyphenyl)-cyclopropanecarboxylate
- Ethyl (1R,2R)-2-(4-Methoxyphenyl)cyclopropanecarboxylate
- NSC55526
- LNIFCHLLDTWCIH-UHFFFAOYSA-N
- J-520619
- ethyl (1S,2S)-2-(4-methoxyphenyl)cyclopropanecarboxylate
- 6142-64-9
- AE-848/00900038
- NSC-55526
- MFCD02258631
- 98017-60-8
- Cyclopropanecarboxylic acid, 2-(4-methoxyphenyl)-, ethyl ester, (1R,2R)-ethyl (1R,2R)-2-(4-methoxyphenyl)cyclopropane-1-carboxylate
- rel-Ethyl (1R,2R)-2-(4-methoxyphenyl)cyclopropane-1-carboxylate
- DTXSID70976980
- CS-0056045
- Ethyl(1S,2S)-2-(4-Methoxyphenyl)cyclopropanecarboxylate
- MFCD31696300
- SY266135
- SY266136
- Z1010778970
- ethyl2-(4-methoxyphenyl)cyclopropanecarboxylate
- AKOS027327746
- ethyl 2-(4-methoxyphenyl)cyclopropane-1-carboxylate
-
- MDL: MFCD02258631
- Inchi: 1S/C13H16O3/c1-3-16-13(14)12-8-11(12)9-4-6-10(15-2)7-5-9/h4-7,11-12H,3,8H2,1-2H3
- InChI Key: LNIFCHLLDTWCIH-UHFFFAOYSA-N
- SMILES: O=C(C1C(C2C=CC(OC)=CC=2)C1)OCC
Computed Properties
- Exact Mass: 220.11000
- Monoisotopic Mass: 220.11
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 16
- Rotatable Bond Count: 5
- Complexity: 244
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 2
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 2.3
- Topological Polar Surface Area: 35.5?2
Experimental Properties
- Density: 1.126
- Boiling Point: 309.4°Cat760mmHg
- Flash Point: 126.3°C
- Refractive Index: 1.531
- PSA: 35.53000
- LogP: 2.36180
- Vapor Pressure: 0.0±0.7 mmHg at 25°C
ethyl 2-(4-methoxyphenyl)cyclopropane-1-carboxylate 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: P264+P280+P305+P351+P338+P337+P313
- Safety Instruction: H303+H313+H333
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
ethyl 2-(4-methoxyphenyl)cyclopropane-1-carboxylate 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%
ethyl 2-(4-methoxyphenyl)cyclopropane-1-carboxylate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | E940713-10mg |
Ethyl 2-(4-Methoxyphenyl)cyclopropanecarboxylate |
98017-60-8 | 10mg |
$ 50.00 | 2022-06-05 | ||
| TRC | E940713-50mg |
Ethyl 2-(4-Methoxyphenyl)cyclopropanecarboxylate |
98017-60-8 | 50mg |
$ 185.00 | 2022-06-05 | ||
| TRC | E940713-100mg |
Ethyl 2-(4-Methoxyphenyl)cyclopropanecarboxylate |
98017-60-8 | 100mg |
$ 275.00 | 2022-06-05 | ||
| abcr | AB444431-1 g |
Ethyl 2-(4-methoxyphenyl)cyclopropanecarboxylate; min. 95% |
98017-60-8 | 1g |
€1,025.00 | 2023-04-22 | ||
| Chemenu | CM111024-100mg |
ethyl 2-(4-methoxyphenyl)cyclopropanecarboxylate |
98017-60-8 | 95% | 100mg |
$*** | 2023-05-29 | |
| Chemenu | CM111024-250mg |
ethyl 2-(4-methoxyphenyl)cyclopropanecarboxylate |
98017-60-8 | 95% | 250mg |
$*** | 2023-05-29 | |
| Chemenu | CM111024-1g |
ethyl 2-(4-methoxyphenyl)cyclopropanecarboxylate |
98017-60-8 | 95% | 1g |
$*** | 2023-05-29 | |
| Alichem | A019125114-250mg |
Ethyl 2-(4-methoxyphenyl)cyclopropanecarboxylate |
98017-60-8 | 95% | 250mg |
$597.32 | 2023-08-31 | |
| Alichem | A019125114-1g |
Ethyl 2-(4-methoxyphenyl)cyclopropanecarboxylate |
98017-60-8 | 95% | 1g |
$1424.80 | 2023-08-31 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1126685-1g |
Ethyl 2-(4-methoxyphenyl)cyclopropane-1-carboxylate |
98017-60-8 | 98% | 1g |
¥2438.00 | 2024-04-23 |
ethyl 2-(4-methoxyphenyl)cyclopropane-1-carboxylate Production Method
Production Method 1
Reaction Conditions
1.1 Reagents: Tetrabutylammonium fluoride Solvents: Tetrahydrofuran ; 30 °C
1.2 Reagents: Sodium hydride Solvents: Dimethyl sulfoxide ; rt
1.2 Reagents: Sodium hydride Solvents: Dimethyl sulfoxide ; rt
Reference
Production Method 2
Reaction Conditions
1.1 Reagents: Sodium dithionite Solvents: Water ; 16 h, pH 7, rt
Reference
- Cyclopropanations via Heme Carbenes: Basic Mechanism and Effects of Carbene Substituent, Protein Axial Ligand, and Porphyrin SubstitutionWei, Yang; Tinoco, Antonio ; Steck, Viktoria; Fasan, Rudi ; Zhang, Yong, Journal of the American Chemical Society (2018, 2018, 140(5), 1649-1662
Production Method 3
Reaction Conditions
1.1 Catalysts: Copper, [dihydrobis(1H-pyrazolato-κN1)borato(1-)-κN2,κN2′]- Solvents: 1,2-Dichloroethane
Reference
- BpCu-Catalyzed Cyclopropanation of Olefins: A Simple System That Operates under Homogeneous and Heterogeneous Conditions (Bp = Dihydridobis(pyrazolyl)borate)Diaz-Requejo, M. Mar; Nicasio, M. Carmen; Perez, Pedro J., Organometallics (1998, 1998, 17(14), 3051-3057
Production Method 4
Reaction Conditions
1.1 Catalysts: 2803878-20-6 Solvents: N,N-Dimethylformamide-d7 ; 30 h, 40 °C
Reference
- A Novel M8L6 Cubic Cage That Binds Tetrapyridyl Porphyrins: Cage and Solvent Effects in Cobalt-Porphyrin-Catalyzed Cyclopropanation ReactionsMouarrawis, Valentinos; Bobylev, Eduard O.; de Bruin, Bas; Reek, Joost N. H., Chemistry - A European Journal (2021, 2021, 27(32), 8390-8397
Production Method 5
Reaction Conditions
1.1 Reagents: Sodium dodecyl sulfate Catalysts: Iron(4+), chloro[[4,4′,4′′,4′′′-(21H,23H-porphine-5,10,15,20-tetrayl)tetrakis[1-… Solvents: Water ; 15 min, rt
1.2 1 h, rt
1.2 1 h, rt
Reference
- Cationic iron porphyrins with sodium dodecyl sulphate for micellar catalysis of cyclopropanation reactionsMaaskant, Ruben V.; Polanco, Ehider A.; van Lier, Roos C. W.; Roelfes, Gerard, Organic & Biomolecular Chemistry (2020, 2020, 18(4), 638-641
Production Method 6
Reaction Conditions
1.1 Reagents: Sodium hydride Solvents: Tetrahydrofuran ; 25 °C; 1 h
1.2 Solvents: Dimethyl sulfoxide ; 12 h, rt
1.3 -
1.2 Solvents: Dimethyl sulfoxide ; 12 h, rt
1.3 -
Reference
- A Gold- and Bronsted Acid Catalytic Interplay Towards the Synthesis of Highly Substituted TetrahydrocarbazolesGarayalde, David; Rusconi, Giulia; Nevado, Cristina, Helvetica Chimica Acta (2017, 2017, 100(3),
Production Method 7
Reaction Conditions
1.1 Catalysts: Palladium diacetate ; rt
Reference
- Intermolecular metal-catalyzed carbenoid cyclopropanationsDavies, Huw M. L.; Antoulinakis, Evan G., Organic Reactions (Hoboken, 2001, ,
Production Method 8
Reaction Conditions
1.1 Catalysts: Ruthenium(1+), aquabromodicarbonyl[1-(5,7-dimethyl-1,8-naphthyridin-2-yl-κN1)-1,… Solvents: Dichloromethane ; 6 h, 40 °C
Reference
- A RuII-N-heterocyclic carbene (NHC) complex from metal-metal singly bonded diruthenium(I) precursor: Synthesis, structure and catalytic evaluationSinha, Arup; Daw, Prosenjit; Rahaman, S. M. Wahidur; Saha, Biswajit; Bera, Jitendra K., Journal of Organometallic Chemistry (2011, 2011, 696(6), 1248-1257
Production Method 9
Reaction Conditions
1.1 Catalysts: 2097677-62-6 Solvents: Dichloromethane ; rt
Reference
- The elusive palladium-diazo adduct captured: synthesis, isolation and structural characterization of [(ArNHC-PPh2)Pd(η2-N2C(Ph)CO2Et)]Rull, Silvia G.; Alvarez, Eleuterio; Fructos, Manuel R.; Belderrain, Tomas R.; Perez, Pedro J., Chemistry - A European Journal (2017, 2017, 23(32), 7667-7671
ethyl 2-(4-methoxyphenyl)cyclopropane-1-carboxylate Raw materials
- Triethyl phosphonoacetate
- Trimethylsulfoxonium iodide
- 4-Methoxycinnamic Acid Ethyl Ester
- Sulfur, iodotrimethyloxo-
- p-Methoxybenzaldehyde
- p-Methoxystyrene
ethyl 2-(4-methoxyphenyl)cyclopropane-1-carboxylate Preparation Products
ethyl 2-(4-methoxyphenyl)cyclopropane-1-carboxylate Suppliers
Amadis Chemical Company Limited
Gold Member
(CAS:98017-60-8)ethyl 2-(4-methoxyphenyl)cyclopropane-1-carboxylate
Order Number:A1095792
Stock Status:in Stock
Quantity:1g
Purity:99%
Pricing Information Last Updated:Thursday, 29 August 2024 20:16
Price ($):399.0
Email:[email protected]
ethyl 2-(4-methoxyphenyl)cyclopropane-1-carboxylate Related Literature
-
José M. Rivera,Mariana Martín-Hidalgo,Jean C. Rivera-Ríos Org. Biomol. Chem., 2012,10, 7562-7565
-
3. 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
-
H. V. Jain,D. Verthelyi,S. L. Beaucage RSC Adv., 2017,7, 42519-42528
-
Doug Ogrin,Laura H. van Poppel,Simon G. Bott,Andrew R. Barron Dalton Trans., 2004, 3689-3694
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Recommended suppliers
Amadis Chemical Company Limited
(CAS:98017-60-8)ethyl 2-(4-methoxyphenyl)cyclopropane-1-carboxylate
Purity:99%
Quantity:1g
Price ($):399.0