iodine monochloride

O=Cc1cc(I)ccc1O
Reaction #2852
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(I)c(CC(=O)O)c1
Reaction #4376
2-iodo-5-methoxybenzeneacetic acid
收率 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
O=c1[nH]c(=O)n([C@H]2CC[C@@H](CO)O2)cc1I
Reaction #4984
iodide
收率 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=S(=O)(c1ccccc1)n1cc(I)c2cc(F)cc(F)c21
Reaction #8210
N-Benzenesulfonyl-3-iodo-5,7-difluoroindole
收率 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(OC)c(C=O)cc1I
Reaction #10849
title compound
收率 87.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1cc(I)c(O)c([N+](=O)[O-])c1
Reaction #42461
title compound
收率 91075.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#Cc1ccc([C@@]2(O)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)cc1Cc1ccc(I)cc1
Reaction #48114
4-(β-D-glucopyranos-1-yl)-2-(4-iodo-benzyl)-benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Nc1ccc(-c2nc3c(F)cccc3s2)cc1I
Reaction #53542
4-Fluoro-2-(4′-amino-3′-iodophenyl)benzothiazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cn1cc(-c2ccnc3c2cc(I)n3S(=O)(=O)c2ccccc2)c(-c2ccc([N+](=O)[O-])cc2)n1
Reaction #57283
title product
收率 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1cc(C(C)C)c(Oc2cnc(N)nc2N)cc1I
Reaction #66632
5-(5-iodo-2-isopropyl-4-methoxy-phenoxy)-pyrimidine-2,4-diamine
收率 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cc(C(C)C)c(S(=O)(=O)c2ccc(C)cc2)cc1I
Reaction #66672
1-Iodo-4-isopropyl-2-methoxy-5-(toluene-4-sulfonyl)-benzene
收率 91.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(O)c1ccc(I)c(O)c1
Reaction #78196
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COC(=O)C(I)CCn1cccc1C(=O)c1ccccc1
Reaction #82182
4-(2-benzoylpyrrol-1-yl)-2-iodobutyric acid methyl ester
收率 91.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1nc(N)nc(N)c1I
Reaction #82526
2,4-diamino-5-iodo-6-methylpyrimidine
收率 73.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=c1[nH]c(=O)n([C@H]2CC[C@@H](CO)O2)cc1I
Reaction #83995
iodide
收率 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Brc1cc2c(cn1)[nH]c1ncc(I)cc12
Reaction #88591
title compound
收率 84.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)S(=O)(=O)c1ccc(-c2cnc3[nH]cc(I)c3n2)cc1
Reaction #155839
sub-title compound
收率 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)c1ccc2c(cnn2S(=O)(=O)c2ccc(C)cc2)c1Nc1ccc(I)cc1F
Reaction #166198
title compound
收率 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)c1ccc2c(cnn2C(=O)OC(C)(C)C)c1Nc1ccc(I)cc1F
Reaction #166205
title compound
收率 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)c1ccc2sncc2c1Nc1ccc(I)cc1F
Reaction #166211
title compound
收率 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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