1,4-diisocyanatobutane

CN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(S(=O)(=O)NCCOCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCOCCNS(=O)(=O)c3cccc(C4CN(C)Cc5c(Cl)cc(Cl)cc54)c3)c2)C1
Reaction #74023
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(S(=O)(=O)NCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCNS(=O)(=O)c3cccc(C4CN(C)Cc5c(Cl)cc(Cl)cc54)c3)c2)C1
Reaction #74040
title compound
Ausbeute 64.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CN1Cc2c(Cl)cc(Cl)cc2C(c2ccc(S(=O)(=O)NCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCNS(=O)(=O)c3ccc(C4CN(C)Cc5c(Cl)cc(Cl)cc54)cc3)cc2)C1
Reaction #74041
title compound
Ausbeute 3.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CN1Cc2c(Cl)cc(Cl)cc2C(c2ccc(S(=O)(=O)NCCOCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCOCCNS(=O)(=O)c3ccc(C4CN(C)Cc5c(Cl)cc(Cl)cc54)cc3)cc2)C1
Reaction #74043
title compound
Ausbeute 64.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1ccc(N=C=O)cc1N=C=O
Reaction #414563
2,4-tolylene diisocyanate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
—
Reaction #452411
phosgenating-aniline formaldehyde
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
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
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
CN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(S(=O)(=O)NCCOCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCOCCNS(=O)(=O)c3cccc(C4CN(C)Cc5c(Cl)cc(Cl)cc54)c3)c2)C1
Reaction #957418
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
CN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(S(=O)(=O)NCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCNS(=O)(=O)c3cccc(C4CN(C)Cc5c(Cl)cc(Cl)cc54)c3)c2)C1
Reaction #957435
title compound
Ausbeute 64.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
CN1Cc2c(Cl)cc(Cl)cc2C(c2ccc(S(=O)(=O)NCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCNS(=O)(=O)c3ccc(C4CN(C)Cc5c(Cl)cc(Cl)cc54)cc3)cc2)C1
Reaction #957436
title compound
Ausbeute 3.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
CN1Cc2c(Cl)cc(Cl)cc2C(c2ccc(S(=O)(=O)NCCOCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCOCCNS(=O)(=O)c3ccc(C4CN(C)Cc5c(Cl)cc(Cl)cc54)cc3)cc2)C1
Reaction #957438
title compound
Ausbeute 64.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
CN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(S(=O)(=O)NCCOCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCOCCNS(=O)(=O)c3cccc(C4CN(C)Cc5c(Cl)cc(Cl)cc54)c3)c2)C1
Reaction #1557365
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
CN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(S(=O)(=O)NCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCNS(=O)(=O)c3cccc(C4CN(C)Cc5c(Cl)cc(Cl)cc54)c3)c2)C1
Reaction #1557382
title compound
Ausbeute 64.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
CN1Cc2c(Cl)cc(Cl)cc2C(c2ccc(S(=O)(=O)NCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCNS(=O)(=O)c3ccc(C4CN(C)Cc5c(Cl)cc(Cl)cc54)cc3)cc2)C1
Reaction #1557383
title compound
Ausbeute 3.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
CN1Cc2c(Cl)cc(Cl)cc2C(c2ccc(S(=O)(=O)NCCOCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCOCCNS(=O)(=O)c3ccc(C4CN(C)Cc5c(Cl)cc(Cl)cc54)cc3)cc2)C1
Reaction #1557385
title compound
Ausbeute 64.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
CN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(S(=O)(=O)NCCOCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCOCCNS(=O)(=O)c3cccc(C4CN(C)Cc5c(Cl)cc(Cl)cc54)c3)c2)C1
Reaction #1566630
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
CN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(S(=O)(=O)NCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCNS(=O)(=O)c3cccc(C4CN(C)Cc5c(Cl)cc(Cl)cc54)c3)c2)C1
Reaction #1566647
title compound
Ausbeute 64.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_08
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