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Iron(II) chloride

Catalog Number
ACM7758943
CAS Number
7758-94-3
Product Name
Iron(II) chloride
Structure
Category
Electrolytes
Synonyms
Ferrous chloride
Iron(II) chloride
7758-94-3
Dichloroiron
FeCl2
Iron(2+) chloride
Iron (II) chloride
Iron(II)chloridetetrahydrate
Iron(II) chloride, anhydrous
Ferrous dichloride
Iron protochloride
Iron chloride (FeCl2)
Iron(II) chloride (1:2)
Fe(II) chloride
iron (11) chloride
Description
Iron(II) chloride, also known as ferrous chloride, is the chemical compound of formula FeCl2. It is a paramagnetic solid with a high melting point. The compound is white, but typical samples are often off-white.
IUPAC Name
Dichloroiron
Molecular Weight
126.75
Molecular Formula
FeCl2
Canonical SMILES
Cl[Fe]Cl
InChI
InChI=1S/2ClH.Fe/h2*1H;/q;+2/p-2
InChI Key
NMCUIPGRVMDVDB-UHFFFAOYSA-L
Boiling Point
1023 °C
Melting Point
677 °C
Flash Point
1023ºC
Purity
99%+
Density
3.16 g/mL at 25 °C (lit.)
Solubility
Soluble in water, alcohol and acetone
Appearance
Greenish white crystalline solid
Application
Ferrous chloride (FeCl2) is used in pharmaceutical preparations, for sewage treatment, and as a mordant (which fixes dyes so that they will not run) in textiles.Aside from use in the laboratory synthesis of iron complexes, ferrous chloride serves as a coagulation and flocculation agent in wastewater treatment, especially for wastes containing chromate or sulfides.It is used for odor control in wastewater treatment. It is used as a precursor to make various grades of hematite that can be used in a variety of pigments. It is the precursor to hydrated iron(III) oxides that are magnetic pigments. FeCl2 finds some use as a reagent in organic synthesis.
Complexity
2.8
Covalently-Bonded Unit Count
1
Defined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Exact Mass
125.872641
Formal Charge
0
Hazard Statements
C:Corrosive
Heavy Atom Count
3
Hydrogen Bond Acceptor Count
0
Hydrogen Bond Donor Count
0
Isotope Atom Count
0
Monoisotopic Mass
125.872641
Odor
Odorless
Rotatable Bond Count
0
Safety Description
S26-S36/37/39-S45
Topological Polar Surface Area
0 Ų
Undefined Atom Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Case Study

Preparation of Iron-Diphosphine Complexes from Iron(II) Chloride for Catalytic Suzuki-Miyaura Coupling

Hatakeyama, Takuji, et al. Journal of the American Chemical Society, 2010, 132.31, 10674-10676.

The transition-metal-catalyzed cross-coupling reaction of organoboron compounds, known as Suzuki-Miyaura coupling, is one of the most prevalent organic synthetic reactions for the production of functional molecules, such as drug intermediates and organic electronic materials. In the presence of iron(II) chloride-diphosphine complexes and magnesium bromide, lithium arylborates react with primary and secondary alkyl halides to give the corresponding coupling products in good to excellent yields.
Iron(II) chloride-diphosphine complexes
· The iron(II) chloride-diphosphine complexes bear one o-phenylene-tethered diphosphine ligand possessing bulky substituents at the 3 and 5 positions of the diphenylphoshino groups.
· The bulky substituents were expected to introduce peripheral steric bulk around the iron center, preventing the formation of coordinatively saturated octahedral iron complexes.

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