sodium cyanamide

N#CNC(=O)c1ccccc1
Reaction #4586
2
المردود 89.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
N#CNC(=O)C12CC3CC(CC(C3)C1)C2
Reaction #4587
4
المردود 85.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCCCCCCCCCCCCCCC(=O)NC#N
Reaction #4588
6
المردود 96.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCCCCCCCCCCCCCCCCC(=O)NC#N
Reaction #4589
Stearoylcyanamide
المردود 92.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
N#CNC(=O)CNC(=O)c1ccccc1
Reaction #4590
N-Benzoylglycylcyanamide
المردود 56.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)C[C@H](NC(=O)c1ccccc1)C(=O)NC#N
Reaction #4592
N-Benzoyl-L-leucylcyanamide
المردود 42.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
N#CNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCC(=O)N1
Reaction #4594
15
المردود 42.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
NC1=NC[C@@H](COc2ccc(C3CCCCC3)cc2)O1
Reaction #309131
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)c1ccc(OC[C@@H]2CN=C(N)O2)cc1
Reaction #324912
(S)-5-(4-tert-butyl-phenoxymethyl)-(4,5-dihydro-oxazol-2-yl)amine
المردود 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
NC1=NCC(COc2ccc(F)cc2)O1
Reaction #324914
5-(4-fluorophenoxymethyl)-(4,5-dihydro-oxazol-2-yl)amine
المردود 37.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC1(C)CCC(c2ccc(OCC3CN=C(N)O3)cc2)CC1
Reaction #324920
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
NC1=NCC(COc2ccc(C3CCOCC3)cc2)O1
Reaction #324922
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
NC1=NCC(COCc2ccccc2)O1
Reaction #324924
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC(C)(C)c1ccc(COCC2CN=C(N)O2)cc1
Reaction #324926
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CN1C(C)(C)CC(c2ccc(OCC3CN=C(N)O3)cc2)CC1(C)C
Reaction #324930
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CC1(COc2ccc(C3CCCCC3)cc2)CNC(=N)O1
Reaction #325049
white solid
المردود 75.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
NC1=NC[C@@H](COCc2ccccc2)O1
Reaction #325061
title compound
المردود 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COC(=O)C1=C(C)NC(C)=C(C(=O)OC)N1c1cccc(NC(=NC#N)NCCCN2CCC(c3ccccc3)CC2)c1
Reaction #654086
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
CCN1CCC[C@@H](CN2CCN(C(=NC#N)Nc3ccc(Cl)c(Cl)c3)CC2)C1
Reaction #690354
title compound
المردود 37.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
CCN(CC)CC1CN=C(N)O1
Reaction #702313
2-Amino-5-diethylaminomethyl-2-oxazoline
المردود 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_02
الصفحة 1التالي