The Synthetic Routes of (6-Chloro-pyridazin-3-yl)-piperidin-3-yl-aMine hydrochloride, 98+% C9H14Cl2N4, MW: 249.14

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Introduction
The synthesis of new

Chlorine

Chlorination

Hydrochloric acid or simply

Hydrochloric

Chlorine

Chlorine

Chlorine

Chlorine

piperidine derivative

Hydrochloride

Hydrochloride

piperidine derivative

piperidine derivative

piperidine derivative

Introduction
The
synthesis of
new

piperidine
derivative

Introduction
The
synthesis
of
new

Chlorine

Chlorination

Hydrochloric
acid
or

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

Introduction
The
synthesis
of
new

piperidine
derivative

Introduction
The
synthesis
of
new

piperidine
derivative

Chlorine

Chlorination

Hydrochloric
acid
or

Hydrochloric
acid
or

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

Introduction
The
synthesis
of
new

piperidine
derivative

Introduction
The
synthesis
of
new

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

Introduction
The
synthesis
of
new

piperidine
derivative

Introduction
The
synthesis
of
new

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

piperidine
derivative

Introduction:

The
synthesis
of
new
piperidine
derivatives
plays
a
crucial
role
in
modern
organic
chemistry.

One
of
the
most
common
methods
involves
chlorination
of
piperidine
using
hydrochloric
acid.

This
article
will
review
the
synthetic
routes
of
(6-chloro-pyridazin-3-yl)-piperidin-3-yl-amine
hydrochloride,
98+%
C9H14Cl2N4,
MW:
249.
14,
in
the
chemical
industry.

Hydrochloric
acid
is
a
strong
acid
that
when
reacts
with
piperidine,
it
can
decompose
to
form
chlorine
gas.

This
chlorine
can
react
with
the
nitrogen
atoms
of
the
piper