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450944

Sigma-Aldrich

Iron(II) chloride

AnhydroBeads, −10 mesh, 99.9% trace metals basis

Synonym(s):

Ferrous chloride, Iron dichloride

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About This Item

Linear Formula:
FeCl2
CAS Number:
Molecular Weight:
126.75
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23
grade:
for synthesis
synthesis grade

grade

for synthesis
synthesis grade

product line

AnhydroBeads

Assay

99.9% trace metals basis

reaction suitability

reagent type: catalyst
core: iron

impurities

≤1500.0 ppm Trace Metal Analysis

particle size

−10 mesh

mp

677 °C (lit.)

density

3.16 g/mL at 25 °C (lit.)

application(s)

battery manufacturing

SMILES string

Cl[Fe]Cl

InChI

1S/2ClH.Fe/h2*1H;/q;;+2/p-2

InChI key

NMCUIPGRVMDVDB-UHFFFAOYSA-L

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Application

Used in the synthesis of a novel cis-Fe(BPE5)2Cl2 (BPE5=1,2-diphospholanoethane) complex, which has potential application in many types of reactions such as intra- or intermolecular activation.

Legal Information

AnhydroBeads is a trademark of Sigma-Aldrich Co. LLC

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1

Storage Class Code

8B - Non-combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

does not flash

Flash Point(C)

does not flash

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

450944-10G-PW:
450944-VAR:
450944-50G:4548173941448
450944-BULK:
450944-50G-PW:
450944-10G:4548173941431


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Field, L.D. et al.
Inorganic Chemistry, 37, 612-612 (1998)
Chong Qin et al.
Angewandte Chemie (International ed. in English), 51(28), 6971-6975 (2012-06-13)
Ironing it out: an efficient and convenient nitrogenation strategy involving C-C bond cleavage for the straightforward synthesis of versatile arylamines is presented. Various alkyl azides and alkylarenes, including the common industrial by-product cumene, react using this protocol. Moreover, this method
Qand Agha Nazari et al.
Journal of pharmacological sciences, 120(2), 105-111 (2012-09-29)
Sodium nitroprusside (SNP) is widely used as a potent vasodilator and a nitric oxide (NO) donor, whereas the cytotoxicity of SNP has been well documented. SNP releases several potentially toxic products such as cyanide anion, NO, and iron. We investigated
Qinqin Xia et al.
The Journal of organic chemistry, 77(20), 9366-9373 (2012-10-03)
Iron-catalyzed direct C-N bond formation between azoles and amides is described. The oxidative coupling reactions of sp(3) C-H bonds adjacent to a nitrogen atom in amides and sulfonamides with the N-H bond in azoles proceeded smoothly in the presence of
Jiangfei Meng et al.
Journal of food science, 77(1), C8-14 (2011-12-21)
Wines made from 3 spine grape (Vitis davidii Foex) genotypes-Junzi 1# (JZ 1#), Junzi 2# (JZ 2#), and Liantang (LT)-and Cherokee rose (Rosa laevigata Michx., CR) were evaluated for their phenolics composition and antioxidant activities by several assays, including 2,2'-azino-bis-(3-ethylbenzothiazoline-6-sulfonic

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