1,3-Dimethyl-2-imidazolidinone (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "1,3-Dimethyl-2-imidazolidinone" in English language version.

refsWebsite

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7doi.org

2^nd place

3worldcat.org

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2acs.org

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2patents.google.com

1,182^nd place

725^th place

1mitsuichemicals.com

low place

1academia.edu

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1rsc.org

2,020^th place

1,872^nd place

1books.google.com

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1springer.com

274^th place

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1harvard.edu

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1nih.gov

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1semanticscholar.org

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1tcichemicals.com

low place

academia.edu (Global: 121^st place; English: 142^nd place)

Barker, Barbara J.; Rosenfarb, Joseph; Caruso, Joseph A. (1979). "Ureas as Solvents for Chemical Investigations". Angewandte Chemie International Edition in English. 18 (7): 503–507. doi:10.1002/anie.197905031. ISSN 1521-3773.

acs.org (Global: 1,248^th place; English: 1,104^th place)

pubs.acs.org

Rosenfarb, Joseph; Huffman, Hugh L. Jr.; Caruso, Joseph A. (1976). "Dielectric constants, viscosities, and related physical properties of several substituted liquid ureas at various temperatures". Journal of Chemical & Engineering Data. 21 (2): 150–153. doi:10.1021/je60069a034. ISSN 0021-9568.
Zaugg, Harold E. (1960). "Specific Solvent Effects in the Alkylation of Enolate Anions. IV. Kinetic Order of Solvent Participation". Journal of the American Chemical Society. 83 (4): 837–840. doi:10.1021/ja01465a025. Retrieved 2025-01-18.

books.google.com (Global: 3^rd place; English: 3^rd place)

Lien, Eric J. (1966). Dipole Moment, Structure and Activity of Cyclic Ureas, Thioureas and Related Compounds. University of California, San Francisco.

doi.org (Global: 2^nd place; English: 2^nd place)

Leahy, Ellen M. "1,3-Dimethyl-2-imidazolidinone" e-EROS Encyclopedia of Reagents for Organic Synthesis (2001),doi:10.1002/047084289X.rd342
Rosenfarb, Joseph; Huffman, Hugh L. Jr.; Caruso, Joseph A. (1976). "Dielectric constants, viscosities, and related physical properties of several substituted liquid ureas at various temperatures". Journal of Chemical & Engineering Data. 21 (2): 150–153. doi:10.1021/je60069a034. ISSN 0021-9568.
Barker, Barbara J.; Rosenfarb, Joseph; Caruso, Joseph A. (1979). "Ureas as Solvents for Chemical Investigations". Angewandte Chemie International Edition in English. 18 (7): 503–507. doi:10.1002/anie.197905031. ISSN 1521-3773.
Boon, W. R. (1947). "Respiratory stimulants. Part I. Fully-substituted ureas derived from αω-alkylenediamines". Journal of the Chemical Society (Resumed): 307–318. doi:10.1039/JR9470000307. ISSN 0368-1769.
Zaugg, Harold E. (1960). "Specific Solvent Effects in the Alkylation of Enolate Anions. IV. Kinetic Order of Solvent Participation". Journal of the American Chemical Society. 83 (4): 837–840. doi:10.1021/ja01465a025. Retrieved 2025-01-18.
Ulrich, Henri (1968), Ulrich, Henri (ed.), "Cyclic Imidoyl Halides", The Chemistry of Imidoyl Halides, New York, NY: Springer US, pp. 193–210, doi:10.1007/978-1-4684-8947-7_8, ISBN 978-1-4684-8947-7, retrieved 2025-01-18{{citation}}: CS1 maint: work parameter with ISBN (link)
Lo, C.-C.; Chao, P.-M. (1990). "Replacement of carcinogenic solvent HMPA by DMI in insect sex pheromone synthesis". Journal of Chemical Ecology. 16 (12): 3245–3253. Bibcode:1990JCEco..16.3245L. doi:10.1007/BF00982095. PMID 24263426. S2CID 9859086.

harvard.edu (Global: 18^th place; English: 17^th place)

ui.adsabs.harvard.edu

Lo, C.-C.; Chao, P.-M. (1990). "Replacement of carcinogenic solvent HMPA by DMI in insect sex pheromone synthesis". Journal of Chemical Ecology. 16 (12): 3245–3253. Bibcode:1990JCEco..16.3245L. doi:10.1007/BF00982095. PMID 24263426. S2CID 9859086.

mitsuichemicals.com (Global: low place; English: low place)

DMI at Mitsui Chemicals

nih.gov (Global: 4^th place; English: 4^th place)

pubmed.ncbi.nlm.nih.gov

Lo, C.-C.; Chao, P.-M. (1990). "Replacement of carcinogenic solvent HMPA by DMI in insect sex pheromone synthesis". Journal of Chemical Ecology. 16 (12): 3245–3253. Bibcode:1990JCEco..16.3245L. doi:10.1007/BF00982095. PMID 24263426. S2CID 9859086.

patents.google.com (Global: 1,182^nd place; English: 725^th place)

rsc.org (Global: 2,020^th place; English: 1,872^nd place)

pubs.rsc.org

Boon, W. R. (1947). "Respiratory stimulants. Part I. Fully-substituted ureas derived from αω-alkylenediamines". Journal of the Chemical Society (Resumed): 307–318. doi:10.1039/JR9470000307. ISSN 0368-1769.

semanticscholar.org (Global: 11^th place; English: 8^th place)

api.semanticscholar.org

Lo, C.-C.; Chao, P.-M. (1990). "Replacement of carcinogenic solvent HMPA by DMI in insect sex pheromone synthesis". Journal of Chemical Ecology. 16 (12): 3245–3253. Bibcode:1990JCEco..16.3245L. doi:10.1007/BF00982095. PMID 24263426. S2CID 9859086.

springer.com (Global: 274^th place; English: 309^th place)

link.springer.com

Ulrich, Henri (1968), Ulrich, Henri (ed.), "Cyclic Imidoyl Halides", The Chemistry of Imidoyl Halides, New York, NY: Springer US, pp. 193–210, doi:10.1007/978-1-4684-8947-7_8, ISBN 978-1-4684-8947-7, retrieved 2025-01-18{{citation}}: CS1 maint: work parameter with ISBN (link)

tcichemicals.com (Global: low place; English: low place)

DMI at TCI

worldcat.org (Global: 5^th place; English: 5^th place)

search.worldcat.org

Rosenfarb, Joseph; Huffman, Hugh L. Jr.; Caruso, Joseph A. (1976). "Dielectric constants, viscosities, and related physical properties of several substituted liquid ureas at various temperatures". Journal of Chemical & Engineering Data. 21 (2): 150–153. doi:10.1021/je60069a034. ISSN 0021-9568.
Barker, Barbara J.; Rosenfarb, Joseph; Caruso, Joseph A. (1979). "Ureas as Solvents for Chemical Investigations". Angewandte Chemie International Edition in English. 18 (7): 503–507. doi:10.1002/anie.197905031. ISSN 1521-3773.
Boon, W. R. (1947). "Respiratory stimulants. Part I. Fully-substituted ureas derived from αω-alkylenediamines". Journal of the Chemical Society (Resumed): 307–318. doi:10.1039/JR9470000307. ISSN 0368-1769.

1,3-Dimethyl-2-imidazolidinone (English Wikipedia)

academia.edu (Global: 121st place; English: 142nd place)

acs.org (Global: 1,248th place; English: 1,104th place)

pubs.acs.org

books.google.com (Global: 3rd place; English: 3rd place)

doi.org (Global: 2nd place; English: 2nd place)

harvard.edu (Global: 18th place; English: 17th place)