Cas no 3299-05-6 (Benzene,(1-ethoxyethyl)-)
Benzene,(1-ethoxyethyl)- structure
Product Name:Benzene,(1-ethoxyethyl)-
Benzene,(1-ethoxyethyl)- Chemical and Physical Properties
Names and Identifiers
-
- Benzene,(1-ethoxyethyl)-
- Benzene, (1-ethoxyethyl)-; AC1L2CLR; 1-phenyl-diethyl ether; ethyl (+/-)-sec-phenylethyl ether; 1-ethoxy-1-phenyl ethane; ethyl 1-phenylethyl ether; (1-ETHOXYETHYL)BENZENE; 1-phenylethyl ethyl ether; Benzene,(1-ethoxyethyl)-; SureCN585596;
- .alpha.-Phenyldiethyl ether
- 2E2F35SUC3
- NS00049611
- 3299-05-6
- MVTKJCAAJPVUHJ-UHFFFAOYSA-N
- ETHYL 1-PHENYLETHYL ETHER
- Benzene, ethoxyethyl-
- EINECS 221-968-2
- NSC 104
- 1-Ethoxy-1-phenylethane
- alpha-Phenyldiethyl ether
- NSC-104
- 1-Phenylethyl ethyl ether
- UNII-2E2F35SUC3
- 1-ethoxyethylbenzene
- (1-Ethoxy-ethyl)-benzene
- .alpha.-Methylbenzyl ethyl ether
- Benzene, (1-ethoxyethyl)-
- Ether, ethyl .alpha.-methylbenzyl
- Phenylather
- DTXSID201347798
- alpha-Methylbenzyl ethyl ether
- SCHEMBL7644979
- NSC104
- (1-ETHOXYETHYL)BENZENE
- SCHEMBL585596
- (1-Ethoxyethyl)benzene #
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- Inchi： 1S/C10H14O/c1-3-11-9(2)10-7-5-4-6-8-10/h4-9H,3H2,1-2H3
- InChI Key： MVTKJCAAJPVUHJ-UHFFFAOYSA-N
- SMILES： O(CC)C(C)C1C=CC=CC=1
Computed Properties
- Exact Mass: 150.10452
- Monoisotopic Mass: 150.104
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 11
- Rotatable Bond Count: 3
- Complexity: 95
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 1
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 9.2A^2
- XLogP3: 2.3
Experimental Properties
- Density: 0.925
- Boiling Point: 183.1°Cat760mmHg
- Flash Point: 60.2°C
- Refractive Index: 1.488
- PSA: 9.23
- LogP: 2.78410
Benzene,(1-ethoxyethyl)- Related Literature
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1. Elaboration of α-substituted benzyl alkyl ethers and sulphides by suppression of the Wittig and related rearrangements via complexation to tricarbonylchromiumJulian Blagg,Stephen G. Davies,Nicholas J. Holman,Charles A. Laughton,Bryan E. Mobbs J. Chem. Soc. Perkin Trans. 1 1986 1581
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Thais Delgado-Abad,Jaime Martínez-Ferrer,Rafael Acerete,Gregorio Asensio,Rossella Mello,María Elena González-Nú?ez Org. Biomol. Chem. 2016 14 6554
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3. 934. Organic peroxides. Part IX. A stereochemical study of the formation of alkyl hydroperoxides from hydrogen peroxideAlwyn G. Davies,R. Feld J. Chem. Soc. 1958 4637
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4. 226. Interaction of boron trichloride with optically active alcohols and ethersW. Gerrard,M. F. Lappert J. Chem. Soc. 1951 1020
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5. The mechanism of thermal eliminations. Part 26. Substituent effects at each carbon of vinyl ethers: non-planarity of the transition stateRoger Taylor J. Chem. Soc. Perkin Trans. 2 1988 737
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