Teilstruktursuche

1243361

Nc1nc(N)c(N=Nc2ccc(Cl)cc2)c(Cl)n1
Reaction #1262
6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidinediamine
Ausbeute 41.4%DOI: 10.6084/m9.figshare.5104873.v1
NNc1cc(OC2CCCC2)c(Cl)cc1F
Reaction #49769
2-fluoro-4-chloro-5-cyclopentyloxyphenylhydrazine
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(Cl)cc1
Reaction #65060
4-Chlorobenzonitrile
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
Oc1cc(Cl)c(Cl)cc1Cl
Reaction #96083
2,4,5-trichlorophenol
DOI: 10.6084/m9.figshare.5104873.v1
NNc1cc(OC2CCCC2)c(Cl)cc1F
Reaction #215740
2-fluoro-4-chloro-5cyclopentyloxyphenylhydrazine
Ausbeute 90.9%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #334534
( V )
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1[nH]c2cc(Cl)c(Cl)cc2c1-c1ccc(Cl)cc1Cl
Reaction #355048
Ethyl 5,6-dichloro-3-(2,4-dichlorophenyl)indole-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)Cc1nc(N)nc(Cl)c1N
Reaction #400766
DOI: 10.1039/C8SC04228D
COC(=O)CC(=O)/C(=N\Nc1ccc(Cl)c(Cl)c1)C(=O)OC
Reaction #473727
(E)-dimethyl 2-(2-(3,4-dichlorophenyl)hydrazono)-3-oxopentanedioate
Ausbeute 97.6%DOI: 10.6084/m9.figshare.5104873.v1
N#[N+]c1ccc(Cl)cc1[N+](=O)[O-].[Cl-]
Reaction #479738
4-Chloro-2-nitrobenzenediazonium Chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(c1ccc(Cl)cc1)c1cc(N=Nc2cc(Cl)ccc2[N+](=O)[O-])c(O)c(C(C)(C)c2ccc(Cl)cc2)c1
Reaction #479742
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Reaction #479743
solid
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(C)(C)c2cc(C(C)(C)C)cc(-n3nc4ccc(Cl)cc4n3)c2O)cc1
Reaction #479745
title compound
DOI: 10.6084/m9.figshare.5104873.v1
F[B-](F)(F)F.N#[N+]c1cc(F)c(Cl)cc1Cl
Reaction #527339
2,4-dichloro-5-fluorophenyldiazonium tetrafluoroborate
DOI: 10.6084/m9.figshare.5104873.v1
N#[N+]c1cc(F)c(Cl)cc1Cl.O=S(=O)([O-])O
Reaction #527341
2,4-dichloro-5-fluorophenyldiazonium hydrogen sulfate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc([N+]#N)c1.[Cl-]
Reaction #549672
m-toluenediazonium chloride
DOI: 10.6084/m9.figshare.5104873.v1
N#[N+]c1ccc(Cl)cc1.[Cl-]
Reaction #563500
4-Chlorophenyldiazonium chloride
DOI: 10.6084/m9.figshare.5104873.v1
N#[N+]c1ccc(Cl)cc1.[Cl-]
Reaction #656636
p-Chlorobenzenediazonium chloride
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
N#[N+]c1ccc(Cl)cc1.[Cl-]
Reaction #741481
4-Chlorobenzenediazonium chloride
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(N)c(N=Nc2ccc(Cl)cc2)c(Cl)n1
Reaction #741482
6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidinediamine
Ausbeute 41.4%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter