1,4-phenylene diisocyanate

FC(F)(F)c1ccon1
Reaction #327991
trifluoromethyl isoxazole
Yield 56.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cc1ccc(N=C=O)cc1N=C=O
Reaction #414563
2,4-tolylene diisocyanate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
CCOC(=O)c1c(COC2CCCCO2)noc1-c1ccccc1Cl
Reaction #436442
title compound
Yield 94.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
—
Reaction #452411
phosgenating-aniline formaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CCc1cc(-c2cnc(SC)c(Cl)c2)on1
Reaction #455474
desired product
Yield 479.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
Cc1ccc(N=C=O)cc1N=C=O
Reaction #460125
2,4-tolylene diisocyanate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_11
Nc1ccccc1
Reaction #523907
aniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_06
—
Reaction #533817
polyisocyanates
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
—
Reaction #535455
polyisocyanates
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
Cc1ccc(N=C=O)cc1N=C=O
Reaction #554138
2,4-tolylene diisocyanate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_10
Cc1ccc(N=C=O)cc1N=C=O
Reaction #574037
2,4-tolylene diisocyanate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_03
—
Reaction #693795
polyisocyanates
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
COc1ccc(COC(=O)CC(c2ccc(OCc3ccc(OC)cc3)cc2)c2ccon2)cc1
Reaction #818390
76.4
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
O=C=Nc1ccc(Cc2ccc(N=C=O)cc2)cc1
Reaction #949318
4,4'diphenylmethane diisocyanate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_02
O=CNc1ccccc1
Reaction #970627
aniline formaldehyde
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
Cc1cc(N(C)C)c2cc(NC(=O)Nc3ccc(NC(=O)Nc4ccc5nc(C)cc(N(C)C)c5c4)cc3)ccc2n1
Reaction #977432
1-(4-dimethylamino-2-methylquinolin-6-yl)-3-{4-[3-(4-dimethylamino-2-methylquinolin-6-yl)ureido]phenyl}urea
Yield 48.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_02
COc1ccc(COC(=O)CC(c2ccc(OCc3ccc(OC)cc3)cc2)c2ccon2)cc1
Reaction #1009382
material
Yield 40.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CCOC(=O)CCCCc1cc(-c2ccccc2OC)on1
Reaction #1126390
orange oil
Yield 97.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
CCOC(=O)CCCCc1cc(-c2cc(Cl)ccc2OC)on1
Reaction #1126395
orange oil
Yield 64.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
COC(=O)CCCc1cc(-c2ccccc2OC)on1
Reaction #1126405
yellow oil
Yield 112.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
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