tributylamine

O=c1[nH]ccc2sccc12
Reaction #2856
title compound
المردود 49.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCC[NH+](CCCC)CCCC.CCCC[NH+](CCCC)CCCC.CCCC[NH+](CCCC)CCCC.O=P([O-])([O-])OP(=O)([O-])O
Reaction #4983
tris(tri-n-butylammonium) pyrophosphate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)C=Cc1ccc2c(-c3c(-c4cccc(C)n4)nn4c3CCC4)ccnc2c1
Reaction #8348
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
—
Reaction #9810
salt
المردود 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCC(CC)CC1(C(=O)Cl)CCCCC1
Reaction #42029
1-(2-ethyl-butyl)-cyclohexanecarbonyl chloride
المردود 95.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C(CCC=O)C(=O)OCC
Reaction #54190
yellow oil
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CC=CN1CCN(C(=O)Cl)C1=O
Reaction #55999
1-chlorocarbonyl-2-oxo-3-propenyl-imidazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
C=C(C(F)(F)F)C(F)(F)F
Reaction #63668
2-trifluoromethyl-3,3,3-trifluoropropene
المردود 75.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
Oc1ccc2c(c1)c(/C=C/c1cnn(CCOC3CCCCO3)c1)nn2C1CCCCO1
Reaction #69792
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #75004
cholesterol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
Nc1cc(O)c2ccccc2n1
Reaction #75229
2-Amino-4-hydroxyquinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
O=[N+]([O-])c1ccc2snc(Cl)c2c1
Reaction #77255
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(C=C2c3ccccc3C(=O)NC2C)cn1
Reaction #77512
rac. 4-[1-(6-methoxy-pyridin-3-yl)-methylidene]-3-methyl-3,4-dihydro-2H-isoquinolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)[C@H]1OC[C@H](Nc2ncc(Cc3ccc(O)nc3)c3ccccc23)CO1
Reaction #77513
trans 1-(2-isopropyl-[1,3]dioxan-5-ylamino)-4-[(6-hydroxy-pyridin-3-yl)methyl]-isoquinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=P([O-])([O-])OP(=O)([O-])OP(=O)([O-])OP(=O)(O)O.O=c1ccn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c(=O)[nH]1.O=c1ccn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c(=O)[nH]1.[NH4+].[NH4+].[NH4+].[NH4+]
Reaction #78833
diuridine tetraphosphate tetraammonium salt
المردود 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCCCOc1ocnc1C
Reaction #79486
4-methyl-5-n-butoxyoxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
C=CC(COC(C)=O)OC(C)=O
Reaction #83002
3,4-diacetoxy-1-butene
المردود 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=c1[nH]ccc2oc(Br)cc12
Reaction #88662
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(NC1CCCCC1)NC1CCCCC1
Reaction #93073
dicyclohexylurea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
O=C(NC1CCCCC1)NC1CCCCC1
Reaction #93074
dicyclohexylurea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
الصفحة 1التالي