hexanediamine

NCCCCCCNC(=O)c1cc2ccc([C@@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)cc2oc1=O
Reaction #215338
N-(6-Aminohexyl)-7-β-galactosylcoumarin-3-carboxamide
المردود 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
—
Reaction #347590
copolymer
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
—
Reaction #462408
copolymer
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
—
Reaction #463089
copolymer
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
CCCCCC(N)N.Nc1nc2ncc(CNc3ccc(C(=O)N[C@@H](CCC(=O)[O-])C(=O)O)cc3)nc2c(=O)[nH]1
Reaction #645234
folate diaminohexane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
—
Reaction #698928
copolymer
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
—
Reaction #813342
copolymer
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_01
CCCCCCCCCCCCCCCCCCOC(=O)CCN(CCCCCCN(CCC(=O)OCCCCCCCCCCCCCCCCCC)C1CC(C)(C)NC(C)(C)C1)C1CC(C)(C)NC(C)(C)C1
Reaction #948848
Compound O
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_02
—
Reaction #951802
powder
المردود 42.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_10
NCCCCCCNC(=O)c1cc2ccc([C@@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)cc2oc1=O
Reaction #1153118
N-(6-Aminohexyl)-7-β-galactosylcoumarin-3-carboxamide
المردود 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_05
CCCCCC(N)N
Reaction #1164732
hexanediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_08
CCCCCC(N)N
Reaction #1168709
hexanediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_12
NCCCCCCNC(=O)c1cc2ccc([C@@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)cc2oc1=O
Reaction #1365340
N-(6-Aminohexyl)-7-β-galactosylcoumarin-3-carboxamide
المردود 10.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_07
—
Reaction #1741737
copolymer
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_04
CCCCCCCCCCCCCCCCCCOC(=O)CCN(CCCCCCN(CCC(=O)OCCCCCCCCCCCCCCCCCC)C1CC(C)(C)NC(C)(C)C1)C1CC(C)(C)NC(C)(C)C1
Reaction #1807647
Compound O
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_04
—
Reaction #1822646
N -1-trifluoroacetylhexanediamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_07
—
Reaction #1823808
powder
المردود 42.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_07
CCCCCCCCCCCCCCCCCCOC(=O)CCN(CCCCCCN(CCC(=O)OCCCCCCCCCCCCCCCCCC)C1CC(C)(C)NC(C)(C)C1)C1CC(C)(C)NC(C)(C)C1
Reaction #1857177
Compound O
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_01
Brc1ccc(-n2c3ccccc3c3ccccc32)c2ccccc12
Reaction #1980282
title compound
المردود 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
c1ccc(-c2ccc3[nH]c4ccc(-c5ccc(-c6cccc7ccccc67)cc5)cc4c3c2)cc1
Reaction #1980285
title compound
المردود 6.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
الصفحة 1التالي