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Page 1
m-[125I]iodoaniline: a useful reagent for radiolabeling biotin.
Khawli LA, Kassis AI. Khawli LA, et al. Int J Rad Appl Instrum B. 1992 Apr;19(3):297-301. doi: 10.1016/0883-2897(92)90114-e. Int J Rad Appl Instrum B. 1992. PMID: 1629019
Biotinyl-m-[125I]iodoanilide (BIA) was synthesized by coupling biotin to m-[125I]iodoaniline via a mixed anhydride reaction. m-[125I]Iodoaniline was produced from the tin precursor, which was prepared using a palladium catalyzed reaction of hexabutylditin with m-bromoan
Biotinyl-m-[125I]iodoanilide (BIA) was synthesized by coupling biotin to m-[125I]iodoaniline via a mixed anhydride reaction. m-[125I]Iodoani …
N-(m-[125I]iodophenyl)maleimide: an agent for high yield radiolabeling of antibodies.
Khawli LA, van den Abbeele AD, Kassis AI. Khawli LA, et al. Int J Rad Appl Instrum B. 1992 Apr;19(3):289-95. doi: 10.1016/0883-2897(92)90113-d. Int J Rad Appl Instrum B. 1992. PMID: 1629018
The unlabeled intermediate was synthesized in greater than or equal to 75% yield using a palladium catalyzed reaction of hexabutylditin with m-bromoaniline, followed by reaction with maleic anhydride and ring annulation. All products were confirmed by NMR and elemen …
The unlabeled intermediate was synthesized in greater than or equal to 75% yield using a palladium catalyzed reaction of hexabutylditin with …
Synthesis of Carboxy ATTO 647N Using Redox Cycling for Xanthone Access.
Bachman JL, Pavlich CI, Boley AJ, Marcotte EM, Anslyn EV. Bachman JL, et al. Org Lett. 2020 Jan 17;22(2):381-385. doi: 10.1021/acs.orglett.9b03981. Epub 2019 Dec 11. Org Lett. 2020. PMID: 31825225 Free PMC article.
This route proceeds in 11 forward steps from 3-bromoaniline with the key xanthone intermediate formed using a new oxidation methodology. ...
This route proceeds in 11 forward steps from 3-bromoaniline with the key xanthone intermediate formed using a new oxidation me …
Relation between photochromic properties and molecular structures in salicylideneaniline crystals.
Johmoto K, Ishida T, Sekine A, Uekusa H, Ohashi Y. Johmoto K, et al. Acta Crystallogr B. 2012 Jun;68(Pt 3):297-304. doi: 10.1107/S0108768112010993. Epub 2012 May 4. Acta Crystallogr B. 2012. PMID: 22610680
The crystal structures of the salicylideneaniline derivatives N-salicylidene-4-tert-butyl-aniline (1), N-3,5-di-tert-butyl-salicylidene-3-methoxyaniline (2), N-3,5-di-tert-butyl-salicylidene-3-bromoaniline (3), N-3,5-di-tert-butyl-salicylidene-3-chloroaniline …
The crystal structures of the salicylideneaniline derivatives N-salicylidene-4-tert-butyl-aniline (1), N-3,5-di-tert-butyl-salicylidene-3-me …
Acute renal and hepatic effects induced by 3-haloanilines in the Fischer 344 rat.
Rankin GO, Valentovic MA, Nicoll DW, Ball JG, Anestis DK, Brown PI, Hubbard JL. Rankin GO, et al. J Appl Toxicol. 1995 Mar-Apr;15(2):139-46. doi: 10.1002/jat.2550150214. J Appl Toxicol. 1995. PMID: 7782560
The decreasing order of in vitro nephrotoxic potential was 3-iodoaniline > 3-bromoaniline > 3-chloroaniline > aniline > 3-fluoroaniline. These results indicate that the 3-haloanilines are not potent nephrotoxicants or hepatotoxicants at sublethal …
The decreasing order of in vitro nephrotoxic potential was 3-iodoaniline > 3-bromoaniline > 3-chloroaniline > …
Development of 3-iodophenylisothiocyanate for radioiodination of monoclonal antibodies.
Ram S, Buchsbaum DJ. Ram S, et al. Int J Rad Appl Instrum A. 1992 Nov;43(11):1387-91. doi: 10.1016/0883-2889(92)90013-5. Int J Rad Appl Instrum A. 1992. PMID: 1333460
The starting material, 3-tri-n-butylstannylphenylisothiocyanate was prepared via a reaction of hexabutylditin with 3-bromoaniline, followed by treatment with thiophosgene with an overall yield of 72%. ...
The starting material, 3-tri-n-butylstannylphenylisothiocyanate was prepared via a reaction of hexabutylditin with 3-bromoaniline
Discovery of anilino-furo[2,3-d]pyrimidine derivatives as dual inhibitors of EGFR/HER2 tyrosine kinase and their anticancer activity.
Hossam M, Lasheen DS, Ismail NSM, Esmat A, Mansour AM, Singab ANB, Abouzid KAM. Hossam M, et al. Eur J Med Chem. 2018 Jan 20;144:330-348. doi: 10.1016/j.ejmech.2017.12.022. Epub 2017 Dec 9. Eur J Med Chem. 2018. PMID: 29275232
Three derivatives bearing 5-carboxylic acid side chain, namely the 3-chloroanilino derivative (8c), the 3-bromoaniline (8d) and the lapatinib analogue (10) demonstrated the most significant submicromolar EGFR inhibition. ...
Three derivatives bearing 5-carboxylic acid side chain, namely the 3-chloroanilino derivative (8c), the 3-bromoaniline (8d) an …
pH-Triggered Molecular Alignment for Reproducible SERS Detection via an AuNP/Nanocellulose Platform.
Wei H, Vikesland PJ. Wei H, et al. Sci Rep. 2015 Dec 11;5:18131. doi: 10.1038/srep18131. Sci Rep. 2015. PMID: 26658696 Free PMC article.
Tests with additional analytes (melamine, 2,4-dichloroaniline, 4-chloroaniline, 3-bromoaniline, and 3-nitroaniline) further illustrate that the AuNP/BC platform provides reproducible analyte detection and quantification while avoiding the uncontrolled aggregation an …
Tests with additional analytes (melamine, 2,4-dichloroaniline, 4-chloroaniline, 3-bromoaniline, and 3-nitroaniline) further il …
Relationship between properties of a series of anilines and their transformation by bacteria.
Paris DF, Wolfe NL. Paris DF, et al. Appl Environ Microbiol. 1987 May;53(5):911-6. doi: 10.1128/aem.53.5.911-916.1987. Appl Environ Microbiol. 1987. PMID: 3606098 Free PMC article.
For the pure-culture and environmental water samples studied, the rate of transformation of the compounds decreased in the following order: aniline greater than 3-bromoaniline greater than 3-chloroaniline greater than 3-methylaniline greater than 3-methoxyaniline gr …
For the pure-culture and environmental water samples studied, the rate of transformation of the compounds decreased in the following order: …
Design, synthesis and evaluation of 2-amino-4-m-bromoanilino-6-arylmethyl-7H-pyrrolo[2,3-d]pyrimidines as tyrosine kinase inhibitors and antiangiogenic agents.
Gangjee A, Zhao Y, Raghavan S, Ihnat MA, Disch BC. Gangjee A, et al. Bioorg Med Chem. 2010 Jul 15;18(14):5261-73. doi: 10.1016/j.bmc.2010.05.049. Epub 2010 May 25. Bioorg Med Chem. 2010. PMID: 20558072 Free PMC article.
Chlorination at the 4-position followed by displacement with 3-bromoaniline or 3-bromo-N-methylaniline and methylation of the 7-NH afforded the target compounds. ...
Chlorination at the 4-position followed by displacement with 3-bromoaniline or 3-bromo-N-methylaniline and methylation of the …
21 results