Teilstruktursuche

[Cl-].[Na+]

CCC1(COS(=O)(=O)c2ccc(C)cc2)COC(=O)N1
Reaction #949
beige solid
DOI: 10.6084/m9.figshare.5104873.v1
OC1CCCCC2(C1)OCCO2
Reaction #1000
3-hydroxycycloheptanone ethylene ketal
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1[C@@H]1CN(Cc2ccccc2)C[C@H]1CO
Reaction #1166
expected product
DOI: 10.6084/m9.figshare.5104873.v1
NC1CCN(C(=O)OCc2ccccc2)CC1
Reaction #1174
4-amino-1-benzyloxycarbonylpiperidine
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C#Cc2ccc([N+](=O)[O-])s2)cc1
Reaction #1723
4-[(5-nitro-2-thienyl)ethynyl]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCc1ccsc1
Reaction #1827
oil
Ausbeute 87.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1C2CCC(=O)C21
Reaction #1861
title compound
Ausbeute 68.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(F)c(F)c(F)c1F
Reaction #1966
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=P([O-])([O-])O.[NH4+].[Na+]
Reaction #2022
Sodium ammonium phosphate
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])[O-].[NH4+].[NH4+]
Reaction #2023
ammonium sulphate
DOI: 10.6084/m9.figshare.5104873.v1
CCC#CCOS(=O)(=O)c1ccc(C)cc1
Reaction #2032
2-pentyn-1-yl p-toluenesulphonate
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCNC(=O)CC(P(=O)(OCC)OCC)P(=O)(OCC)OCC
Reaction #2068
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(OCC)C(C)CCCCOC1CCCCO1
Reaction #2110
Diethyl 1-methyl-5-(tetrahydropyran-2-yloxy)pentylphosphonate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](C)Oc1ccccc1C=Cc1cc2ccccc2n1C
Reaction #2244
(S)-2-{2[2-(1-methoxycarbonylethoxy)phenyl]vinyl}-1-methylindole
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CN(c2ccncc2)CCN1c1ccc(OCc2ccccc2)cc1
Reaction #2348
4-benzyloxy [4-(4-pyridyl)piperazin-2-one-1-yl]benzene
Ausbeute 123.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)C1CCN(CCN(C(=O)c2ccc([N+](=O)[O-])cc2)c2cccnc2)CC1
Reaction #2613
title compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncoc1C(=O)c1ccoc1
Reaction #2891
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #2901
( a )
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1C[C@@H](C(=O)O)N(C(=O)OC(C)(C)C)C1=O
Reaction #2977
product
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(/C=C\c2ccc(Cl)c([N+](=O)[O-])c2)cc(OC)c1OC
Reaction #2993
intended compound
Ausbeute 50.9%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter