Участвует в 9 реакциях

C(CSSCCN)N.Cl

C=C(C)C(=O)OCC(C)O
Reaction #48472
HPMA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1c2cccc3c(Cl)ccc(c23)C(=O)N1CCSSCCN1C(=O)c2cccc3c(Cl)ccc(c23)C1=O
Reaction #507595
2,2′-(disulfanediyldiethane-2,1-diyl)bis(6-chloro-1H-benzo[de]-isoquinoline-1,3(2H)-dione)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
O=C1c2cccc3c(Cl)ccc(c23)C(=O)N1CCSSCCN1C(=O)c2cccc3c(Cl)ccc(c23)C1=O
Reaction #1130533
2,2′-(Disulphanediyldiethane-2,1-diyl)bis(6-chloro-1H-benzo[de]-isoquinoline-1,3(2H)-dione)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
C=C(C)C(=O)OCC(C)O
Reaction #1697085
HPMA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_01
O=C1c2cccc3c(Cl)ccc(c23)C(=O)N1CCSSCCN1C(=O)c2cccc3c(Cl)ccc(c23)C1=O
Reaction #1751263
2,2′-(Disulphanediyldiethane-2,1-diyl)bis(6-chloro-1H-benzo[de]-isoquinoline-1,3(2H)-dione)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_10
O=C1c2cccc3c(Cl)ccc(c23)C(=O)N1CCSSCCN1C(=O)c2cccc3c(Cl)ccc(c23)C1=O
Reaction #2278356
2,2′-(Disulphanediyldiethane-2,1-diyl)bis(6-chloro-1H-benzo[de]-isoquinoline-1,3(2H)-dione)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_12
O=C(CCCCl)NCCSSCCNC(=O)CCCCl
Reaction #2324520
N,N′-(disulfanediyldiethane-2,1-diyl)bis(4-chlorobutanamide)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_05
O=C1c2cccc3c(Cl)ccc(c23)C(=O)N1CCSSCCN1C(=O)c2cccc3c(Cl)ccc(c23)C1=O
Reaction #2446057
2,2′-(Disulphanediyldiethane-2,1-diyl)bis(6-chloro-1H-benzo[de]-isoquinoline-1,3(2H)-dione)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_04
O=C(CCCCl)NCCSSCCNC(=O)CCCCl
Reaction #2513000
N,N′-(disulfanediyldiethane-2,1-diyl)bis(4-chlorobutanamide)
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_06