4-chlorobenzenediazonium chloride

Nc1nc(N)c(N=Nc2ccc(Cl)cc2)c(Cl)n1
Reaction #1262
6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidinediamine
Yield 41.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #334534
( V )
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_11
Cc1cccc([N+]#N)c1.[Cl-]
Reaction #549672
m-toluenediazonium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_05
N#[N+]c1ccc(Cl)cc1.[Cl-]
Reaction #563500
4-Chlorophenyldiazonium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
N#[N+]c1ccc(Cl)cc1.[Cl-]
Reaction #656636
p-Chlorobenzenediazonium chloride
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_03
N#[N+]c1ccc(Cl)cc1.[Cl-]
Reaction #741481
4-Chlorobenzenediazonium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_07
Nc1nc(N)c(N=Nc2ccc(Cl)cc2)c(Cl)n1
Reaction #741482
6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidinediamine
Yield 41.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_07
Nc1nc(Cl)c(N=Nc2ccc(Cl)cc2)c(N[C@H]2C=C[C@@H](CO)C2)n1
Reaction #815826
title compound
Yield 6623.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_09
N#[N+]c1ccc(Cl)cc1.[Cl-]
Reaction #980786
4-Chlorobenzenediazonium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_06
Nc1nc(N)c(N=Nc2ccc(Cl)cc2)c(Cl)n1
Reaction #980787
6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidinediamine
Yield 41.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_06
N#[N+]c1ccc(Cl)cc1.[Cl-]
Reaction #1060541
p-Chlorobenzenediazonium chloride
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_11
Nc1nc(Cl)c(N=Nc2ccc(Cl)cc2)c(N[C@H]2C=C[C@@H](CO)C2)n1
Reaction #1174214
title compound
Yield 137.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_07
Nc1nc(Cl)c(N=Nc2ccc(Cl)cc2)c(N[C@H]2C=C[C@@H](CO)C2)n1
Reaction #1621329
title compound
Yield 137.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_02
Nc1nc(Cl)c(N=Nc2ccc(Cl)cc2)c(N[C@H]2C=C[C@@H](CO)C2)n1
Reaction #1621577
title compound
Yield 137.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_02
Nc1nc(Cl)c(N=Nc2ccc(Cl)cc2)c(N[C@H]2C=C[C@@H](CO)C2)n1
Reaction #1678595
title compound
Yield 137.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_04
N#[N+]c1ccc(Cl)cc1.[Cl-]
Reaction #2168977
4-Chlorobenzenediazonium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_02
Nc1nc(N)c(N=Nc2ccc(Cl)cc2)c(Cl)n1
Reaction #2168978
6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidinediamine
Yield 41.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_02