Dimethylformamide (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Dimethylformamide" in English language version.

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12doi.org

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4nih.gov

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3harvard.edu

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aist.go.jp

"Dimethylformamide". Spectral Database for Organic Compounds. Japan: AIST. Retrieved 2012-06-28.^{[permanent dead link]}

archive.org

Clayden, J. (2001). Organic Chemistry. Oxford: Oxford University Press. pp. 276–296. ISBN 0-19-850346-6.

books.google.com

Walter Leitner; Philip G. Jessop (1999). Chemical synthesis using supercritical fluids. Wiley-VCH. pp. 408–. ISBN 978-3-527-29605-7. Retrieved 27 June 2011.
Li, Jie Jack (2014). "Bouveault aldehyde synthesis". Name Reactions: A Collection of Detailed Mechanisms and Synthetic Applications (5th ed.). Springer Science & Business Media. pp. 72–73. ISBN 978-3-319-03979-4.

cdc.gov

NIOSH Pocket Guide to Chemical Hazards. "#0226". National Institute for Occupational Safety and Health (NIOSH).
"Dimethylformamide". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).

doi.org

Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. pp. 841, 844. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4. The traditional name 'formamide' is retained for HCO-NH₂ and is the preferred IUPAC name. Substitution is permitted on the –NH₂ group.
H. S. Gutowsky; C. H. Holm (1956). "Rate Processes and Nuclear Magnetic Resonance Spectra. II. Hindered Internal Rotation of Amides". J. Chem. Phys. 25 (6): 1228–1234. Bibcode:1956JChPh..25.1228G. doi:10.1063/1.1743184.
Bipp, H.; Kieczka, H. "Formamides". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a12_001.pub2. ISBN 978-3-527-30673-2.
Taft, R. W.; Abraham, M. H.; Doherty, R. M.; Kamlet, M. J. (1985). "The molecular properties governing solubilities of organic nonelectrolytes in water". Nature. 313 (6001): 384–386. Bibcode:1985Natur.313..384T. doi:10.1038/313384a0. S2CID 36740734.
Comins, Daniel L.; Joseph, Sajan P. (2001). "N,N-Dimethylformamide". N,N-Dimethylformamide. Encyclopedia of Reagents for Organic Synthesis. John Wiley & Sons. doi:10.1002/047084289x.rd335. ISBN 9780470842898.
Vilsmeier, Anton; Haack, Albrecht (1927). "Über die Einwirkung von Halogenphosphor auf Alkyl-formanilide. Eine neue Methode zur Darstellung sekundärer und tertiärer p-Alkylamino-benzaldehyde" [On the reaction of phosphorus halides with alkyl formanilides. A new method for the preparation of secondary and tertiary p-alkylamino-benzaldehyde]. Ber. Dtsch. Chem. Ges. A/B (in German). 60 (1): 119–122. doi:10.1002/cber.19270600118.
Meth-Cohn, Otto; Stanforth, Stephen P. (1993). "The Vilsmeier-Haack Reaction". In Trost, Barry M.; Heathcock, Clayton H. (eds.). Additions to CX π-Bonds, Part 2. Comprehensive Organic Synthesis: Selectivity, Strategy and Efficiency in Modern Organic Chemistry. Vol. 2. Elsevier. pp. 777–794. doi:10.1016/B978-0-08-052349-1.00049-4. ISBN 9780080405933.
Jones, Gurnos; Stanforth, Stephen P. (2000). "The Vilsmeier Reaction of Non-Aromatic Compounds". Org. React. 56 (2): 355–686. doi:10.1002/0471264180.or056.02.
Vogel G. C.; Drago, R. S. (1996). "The ECW Model". Journal of Chemical Education. 73 (8): 701–707. Bibcode:1996JChEd..73..701V. doi:10.1021/ed073p701.
Cramer, R. E.; Bopp, T. T. (1977). "Graphical display of the enthalpies of adduct formation for Lewis acids and bases". Journal of Chemical Education. 54: 612–613. doi:10.1021/ed054p612. The plots shown in this paper used older parameters. Improved E&C parameters are listed in ECW model.
Lyle, W. H.; Spence, T. W.; McKinneley, W. M.; Duckers, K. (1979). "Dimethylformamide and alcohol intolerance". British Journal of Industrial Medicine. 36 (1): 63–66. doi:10.1136/oem.36.1.63. PMC 1008494. PMID 444443.
Redlich, C.; Beckett, W. S.; Sparer, J.; Barwick, K. W.; Riely, C. A.; Miller, H.; Sigal, S. L.; Shalat, S. L.; Cullen, M. R. (1988). "Liver disease associated with occupational exposure to the solvent dimethylformamide". Annals of Internal Medicine. 108 (5): 680–686. doi:10.7326/0003-4819-108-5-680. PMID 3358569.

harvard.edu

ui.adsabs.harvard.edu

H. S. Gutowsky; C. H. Holm (1956). "Rate Processes and Nuclear Magnetic Resonance Spectra. II. Hindered Internal Rotation of Amides". J. Chem. Phys. 25 (6): 1228–1234. Bibcode:1956JChPh..25.1228G. doi:10.1063/1.1743184.
Taft, R. W.; Abraham, M. H.; Doherty, R. M.; Kamlet, M. J. (1985). "The molecular properties governing solubilities of organic nonelectrolytes in water". Nature. 313 (6001): 384–386. Bibcode:1985Natur.313..384T. doi:10.1038/313384a0. S2CID 36740734.
Vogel G. C.; Drago, R. S. (1996). "The ECW Model". Journal of Chemical Education. 73 (8): 701–707. Bibcode:1996JChEd..73..701V. doi:10.1021/ed073p701.

hathitrust.org

babel.hathitrust.org

Verley, A. (1893). "Sur la préparation des amides en général" [On the preparation of amides in general]. Bulletin de la Société Chimique de Paris. 3rd series (in French). 9: 690–692. On p. 692, Verley states that DMF is prepared by a procedure analogous to that for the preparation of dimethylacetamide (see p. 691), which would be by distilling dimethylamine hydrochloride and potassium formate.
Bouveault, Louis (1904). "Modes de formation et de préparation des aldéhydes saturées de la série grasse" [Methods of preparation of saturated aldehydes of the aliphatic series]. Bulletin de la Société Chimique de Paris. 3rd series (in French). 31: 1306–1322.
Bouveault, Louis (1904). "Nouvelle méthode générale synthétique de préparation des aldéhydes" [Novel general synthetic method for preparing aldehydes]. Bulletin de la Société Chimique de Paris. 3rd series (in French). 31: 1322–1327.

mst.dk

Magnus Løfstedt. "Skumlegetøj afgiver farlige kemikalier (in English- Squishies giving dangerous chemicals)". Archived from the original on 2021-09-03. Retrieved 2019-06-13.

nih.gov

pubmed.ncbi.nlm.nih.gov

Lyle, W. H.; Spence, T. W.; McKinneley, W. M.; Duckers, K. (1979). "Dimethylformamide and alcohol intolerance". British Journal of Industrial Medicine. 36 (1): 63–66. doi:10.1136/oem.36.1.63. PMC 1008494. PMID 444443.
Redlich, C.; Beckett, W. S.; Sparer, J.; Barwick, K. W.; Riely, C. A.; Miller, H.; Sigal, S. L.; Shalat, S. L.; Cullen, M. R. (1988). "Liver disease associated with occupational exposure to the solvent dimethylformamide". Annals of Internal Medicine. 108 (5): 680–686. doi:10.7326/0003-4819-108-5-680. PMID 3358569.

pubchem.ncbi.nlm.nih.gov

"Hazardous Substances Data Bank (HSDB) - N,N-DIMETHYLFORMAMIDE".

ncbi.nlm.nih.gov

Lyle, W. H.; Spence, T. W.; McKinneley, W. M.; Duckers, K. (1979). "Dimethylformamide and alcohol intolerance". British Journal of Industrial Medicine. 36 (1): 63–66. doi:10.1136/oem.36.1.63. PMC 1008494. PMID 444443.

nist.gov

wtt-pro.nist.gov

N,N-Dimethylmethanamide, NIST web thermo tables

nist.gov

Haddon, R.; Itkis, M. (March 2008). "3. Near-Infrared (NIR) Spectroscopy" (pdf). In Freiman, S.; Hooker, S.; Migler; K.; Arepalli, S. (eds.). Publication 960-19 Measurement Issues in Single Wall Carbon Nanotubes. NIST. p. 20. Retrieved 2012-06-28.

semanticscholar.org

api.semanticscholar.org

Taft, R. W.; Abraham, M. H.; Doherty, R. M.; Kamlet, M. J. (1985). "The molecular properties governing solubilities of organic nonelectrolytes in water". Nature. 313 (6001): 384–386. Bibcode:1985Natur.313..384T. doi:10.1038/313384a0. S2CID 36740734.

web.archive.org

Magnus Løfstedt. "Skumlegetøj afgiver farlige kemikalier (in English- Squishies giving dangerous chemicals)". Archived from the original on 2021-09-03. Retrieved 2019-06-13.