Naphthalene, 2-propyl-
- Formula: C13H14
- Molecular weight: 170.2503
- IUPAC Standard InChI: InChI=1S/C13H14/c1-2-5-11-8-9-12-6-3-4-7-13(12)10-11/h3-4,6-10H,2,5H2,1H3
- IUPAC Standard InChIKey: LQBNOHAXLHRIQW-UHFFFAOYSA-N
- CAS Registry Number: 2027-19-2
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
View 3d structure (requires JavaScript / HTML 5) - Other names: 2-Propylnaphthalene
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Normal boiling point
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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
| Tboil (K) | Reference | Comment |
|---|---|---|
| 547.9 | Romadane, 1957 | Uncertainty assigned by TRC = 2. K; TRC |
| 541. | Luther, 1955 | Uncertainty assigned by TRC = 5. K; TRC |
| 546.7 | Anderson, Smith, et al., 1953 | Uncertainty assigned by TRC = 3. K; TRC |
| 546.7 | Bailey, Pickering, et al., 1949 | Uncertainty assigned by TRC = 1.5 K; TRC |
| 547. | Morrell, Pickering, et al., 1948 | Uncertainty assigned by TRC = 2. K; TRC |
| 551. | Vavon and Mottez, 1944 | Uncertainty assigned by TRC = 6. K; TRC |
| 551. | Bargellini and Melacini, 1908 | Uncertainty assigned by TRC = 6. K; 1935 robdav 0 found that this was probably 1-propylnaphth.; TRC |
| 551. | Bargellini and Melacini, 1908, 2 | Uncertainty assigned by TRC = 6. K; 1935 robdav 0 found that this was probably 1-propylnaphth.; TRC |
References
Go To: Top, Normal boiling point, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Romadane, 1957
Romadane, I.,
Zh. Obshch. Khim., 1957, 27, 1833. [all data]
Luther, 1955
Luther, H.,
Private Communication 1955, 1955. [all data]
Anderson, Smith, et al., 1953
Anderson, D.G.; Smith, J.C.; Rallings, R.J.,
J. Chem. Soc., 1953, 1953, 443. [all data]
Bailey, Pickering, et al., 1949
Bailey, A.S.; Pickering, G.B.; Smith, J.C.,
Alkylnaphthalenes: III the n-butyl, amyl, and hexylnaphthalenes,
J. Inst. Pet., 1949, 35, 103-17. [all data]
Morrell, Pickering, et al., 1948
Morrell, S.H.; Pickering, G.B.; Smith, J.C.,
Alkylnaphthalenes II. The Methyl-, Ethyl-, and Propylnaphthalenes,
J. Inst. Pet., 1948, 34, 677. [all data]
Vavon and Mottez, 1944
Vavon, G.; Mottez, P.,
Action of Halogenated Derivatives on Aromatic Magnesium Halides in the Presence of FeCl3,
C. R. Hebd. Seances Acad. Sci., 1944, 218, 557. [all data]
Bargellini and Melacini, 1908
Bargellini, G.; Melacini, G.,
Atti R. Accad. Naz. Lincei, Mem. Cl. Sci. Fis., Mat. Nat., 1908, 17, 26. [all data]
Bargellini and Melacini, 1908, 2
Bargellini, G.; Melacini, G.,
Gazz. Chim. Ital, 1908, 36, 567. [all data]
Notes
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- Symbols used in this document:
Tboil Boiling point - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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