{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,25]],"date-time":"2025-11-25T20:39:50Z","timestamp":1764103190658,"version":"3.37.3"},"reference-count":14,"publisher":"International Union of Crystallography (IUCr)","issue":"4","license":[{"start":{"date-parts":[[2021,4,20]],"date-time":"2021-04-20T00:00:00Z","timestamp":1618876800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/legalcode"},{"start":{"date-parts":[[2021,4,20]],"date-time":"2021-04-20T00:00:00Z","timestamp":1618876800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/legalcode"}],"content-domain":{"domain":["iucr.org","wiley.com","iucrj.org"],"crossmark-restriction":true},"short-container-title":["IUCrData","IUCr Data","International Union Crystallogr Data","Int Union Cryst Data"],"accepted":{"date-parts":[[2021,4,12]]},"published-print":{"date-parts":[[2021,4,28]]},"abstract":"<jats:p>In the title solvated crystal, C<jats:sub>8<\/jats:sub>H<jats:sub>5<\/jats:sub>Br<jats:sub>2<\/jats:sub>NO<jats:sub>3<\/jats:sub>\u00b7C<jats:sub>3<\/jats:sub>H<jats:sub>8<\/jats:sub>O, the acid molecules form inversion dimers by pairwise N\u2014H...O hydrogen bonds between carbamoyl groups and the carboxyl and carbamoyl groups link to form head-to-tail inversion dimers. The 2-propanol hydroxyl group interposes between adjacent head-tail pairs, resulting in <jats:italic>C<\/jats:italic>\n                  <jats:sub>3<\/jats:sub>\n                  <jats:sup>3<\/jats:sup>(10) chains of hydrogen bonds propagating along [100]. The molecules of 2-propanol are disordered over two sets of sites in a 0.598\u2005(8):0.402\u2005(8) ratio. The best-fit planes of the carbamoyl group and benzene ring are inclined by 88.26\u2005(11)\u00b0. This is a greater inclination than was previously reported with CH<jats:sub>3<\/jats:sub>, Cl, F or H in place of the Br atoms, although those analogues did not have a <jats:italic>para<\/jats:italic> carboxyl group.<\/jats:p>","DOI":"10.1107\/s2414314621003916","type":"journal-article","created":{"date-parts":[[2021,4,20]],"date-time":"2021-04-20T07:59:58Z","timestamp":1618905598000},"update-policy":"https:\/\/doi.org\/10.1107\/cm_01","source":"Crossref","is-referenced-by-count":1,"title":["3,5-Dibromo-4-carbamoylbenzoic acid 2-propanol monosolvate"],"prefix":"10.1107","volume":"6","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8183-0767","authenticated-orcid":true,"given":"Wayland E.","family":"Noland","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ryan J.","family":"Herzig","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Renee J.","family":"Fox","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4554-6707","authenticated-orcid":true,"given":"Kenneth J.","family":"Tritch","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"329","published-online":{"date-parts":[[2021,4,20]]},"reference":[{"key":"hb4381_bb1","doi-asserted-by":"crossref","first-page":"2201","DOI":"10.1107\/S0567740872005801","volume":"28","author":"Blake","year":"1972","journal-title":"Acta Cryst. 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