Substructure Search

7410

CCOCn1cnc2c1c(=O)n(CCCCCP(=O)(OCC)OCC)c(=O)n2C
Reaction #2104
Diethyl [5-(7-ethoxymethyl-3-methylxanthin-1-yl)pentyl]phosphonate
DOI: 10.6084/m9.figshare.5104873.v1
CCCn1cnc2c1c(=O)n(CCCCCP(=O)(OCC)OCC)c(=O)n2C
Reaction #2105
Diethyl [5-(3-methyl-7-propylxanthin-1-yl)-pentyl]phosphonate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)c1ccc(N2CCCCC2)cc1
Reaction #10880
2-bromo-1-[4-(1-piperidinyl)phenyl]ethanone
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(C(=O)OC)nc2-c2ccncc2)cc1
Reaction #40820
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(C(=O)OC)nc2-c2ccccn2)cc1
Reaction #40821
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccc(Nc2nc3cc(OC4(C(=O)O)C=CC=CN4)ccc3n2C)cc1
Reaction #41736
2-{[4-(dimethylamino)phenylamino)-1-methylbenzimidazol-5-yloxy)pyridin-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCO[Si](CCP(=O)(OCC)OCC)(OCC)OCC
Reaction #42004
(EtO)3SiCH2CH2PO(OEt)2
Yield 33.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc2nn[nH]c2cc1[N+](=O)[O-]
Reaction #46054
[ 19 ]
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CNCc1cccnc1-c1cc(C(C)(C)C)c(O)c(C(C)(C)C)c1)OCC
Reaction #49892
compound
Yield 66.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(CNC(CCc1ccccc1)c1cc(C(C)(C)C)c(OC)c(C(C)(C)C)c1)OCC
Reaction #49894
yellow oil
Yield 37.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(OCC)c1ccc(C(NC(=O)OC(C)(C)C)C(=O)OCc2ccccc2)cc1
Reaction #61088
tert-butoxycarbonylamino-[4-(diethoxy-phosphoryl)-phenyl]-acetic acid benzyl ester
Yield 93.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccc([N+](=O)[O-])c(N2CCCCC2)c1
Reaction #61172
title compound
Yield 27.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1ccc(NC)c(N2CCCCC2)c1
Reaction #61173
title compound
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCCC(=O)c1ccc(OC)c(OC)c1OC
Reaction #62231
product
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC(=O)c1ccc(OC)c(OC)c1OC
Reaction #62236
55
Yield 72.7%DOI: 10.6084/m9.figshare.5104873.v1
COCC(=O)C(O)(CC(=O)[O-])C[N+](C)(C)C.[Cl-]
Reaction #63654
methoxy acetyl carnitine chloride
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOCC(=O)C(O)(CC(=O)[O-])C[N+](C)(C)C.[Cl-]
Reaction #63655
title compound
Yield 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCOP(=O)(O)O[C@H](CC(=O)O)C[N+](C)(C)C.[OH-]
Reaction #64412
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #64421
salt
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)N1CCN(c2ccc([N+](=O)[O-])cc2)CC1
Reaction #66122
2,2-dimethyl-1-[4-(4-nitro-phenyl)-piperazin-1-yl]-propan-1-one
Yield 85.8%DOI: 10.6084/m9.figshare.5104873.v1
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