Iron(III) chloride hexahydrate

Base Information

• Chemical Name: Iron(III) chloride hexahydrate
• CAS No.: 10225-77-1
• Molecular Formula: C₂₇H₂₄O₈
• Molecular Weight: 476.483
• European Community (EC) Number: 958-611-1
• Wikidata: Q27159033
• Mol file: 10225-77-1.mol

Synonyms:10225-77-1;FERRIC CHLORIDE, 6-HYDRATE;Iron(III) chloride hexahydrate;Iron trichloride hexahydrate;MFCD00149712;Iron (III) Chloride Hexahydrate;trichloroiron;hexahydrate;trichloroiron hexahydrate;FeCl3.6H2O;Iron(III)chloride hexahydrate;trichloroiron--water (1/6);iron(III)-chloride hexahydrate;CHEBI:86254;Iron( cento) chloride hexahydrate;iron(III) trichloride hexahydrate;7705-08-0 (anhyd.);Lyxopyranoside, methyl, tribenzoate;AKOS015903724;Iron(III) chloride hexahydrate, 98%;A919942;Iron(III) chloride hexahydrate, ACS reagent, 97%;Q27159033;Iron(III) chloride hexahydrate, p.a., 97.0-102.0%;Iron(III) chloride hexahydrate, SAJ first grade, >=98.0%;Iron(III) chloride hexahydrate, JIS special grade, >=99.0%;Iron(III) chloride hexahydrate, reagent grade, >=98%, chunks;Iron(III) chloride hexahydrate, Vetec(TM) reagent grade, 98%;Iron(III) chloride hexahydrate, puriss. p.a., Reag. Ph. Eur., >=99%;Iron(III) chloride hexahydrate, puriss. p.a., ACS reagent, crystallized, 98.0-102% (RT)

Chemical Property of Iron(III) chloride hexahydrate

Chemical Property:

• Vapor Pressure: 1 mm Hg ( 194 °C)
• Melting Point: 37 °C(lit.)
• Boiling Point: 280-285 °C(lit.)
• PSA: 97.36000
• Density: 1.32±0.1 g/cm3(Predicted)
• LogP: 3.66590
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 0
• Exact Mass: 268.904882
• Heavy Atom Count: 10
• Complexity: 8

Purity/Quality:

98%,99%, ^*data from raw suppliers

Safty Information:

• Hazard Codes: Xn
• Statements: 22-38-41
• Safety Statements: 26-39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: O.O.O.O.O.O.Cl[Fe](Cl)Cl

Technology Process of Iron(III) chloride hexahydrate

There total 18 articles about Iron(III) chloride hexahydrate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

1,3,5-tri-O-benzoyl-α-D-ribofuranoside (22224-41-5) → methyl tri-O-benzoyl-α-D-arabinopyranoside (6638-76-2,10225-75-9,10225-76-0,10225-77-1,10225-78-2,13035-45-5,32445-39-9,33640-74-3,88165-09-7,88165-10-0,145306-49-6)

Guidance literature:

Multi-step reaction with 3 steps

1: pyridine

2: sodium methylate; methanol; dichloromethane

3: pyridine

With pyridine; methanol; dichloromethane; sodium methylate;

DOI:10.1021/ja01599a048

Reference yield:

methanol (67-56-1) + 2,3,4-tri-O-benzoyl-β-D-ribopyranosyl bromide (13035-44-4,13035-48-8,14206-56-5,14262-83-0,40010-17-1,50271-21-1,58407-63-9,60426-89-3,90365-68-7,108508-31-2,108942-37-6,145374-03-4) → methyl 2,3,4-tri-O-benzoyl-β-D-ribopyranoside (6638-76-2,10225-75-9,10225-76-0,10225-77-1,10225-78-2,13035-45-5,32445-39-9,33640-74-3,88165-09-7,88165-10-0,145306-49-6)

Guidance literature:

DOI:10.1021/ja01192a025

Reference yield:

tetra-O-benzoyl-β-D-ribopyranose (7473-43-0) → methyl 2,3,4-tri-O-benzoyl-β-D-ribopyranoside (6638-76-2,10225-75-9,10225-76-0,10225-77-1,10225-78-2,13035-45-5,32445-39-9,33640-74-3,88165-09-7,88165-10-0,145306-49-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 1,2-dichloro-ethane; hydrogen bromide; acetic acid

With hydrogen bromide; acetic acid; 1,2-dichloro-ethane;

DOI:10.1021/ja01192a025

upstream raw materials:

benzoyl chloride

(2S,3S,4R,5R)-2-Methoxy-tetrahydro-pyran-3,4,5-triol

methanol

2,3,4-tri-O-benzoyl-β-D-arabinopyranosyl bromide

Downstream raw materials:

(2S,3S,4R,5R)-2-Methoxy-tetrahydro-pyran-3,4,5-triol

methyl-(O³,O⁴-dibenzoyl-O²-methanesulfonyl-α-D-arabinopyranoside)

methyl-(O³,O⁴-isopropyliden-α-D-arabinopyranoside)

methyl 2-O-methanesulfonyl-α-D-arabinopyranoside

Refernces

Synthesis, characterization and antimicrobial activity of some transition metal complexes of N-(5-chloro-2-hydroxyphenyl)-3-methoxy-salicylaldimine

10.4314/bcse.v29i1.6

The study focuses on the synthesis, characterization, and antimicrobial activity of transition metal complexes derived from N-(5-chloro-2-hydroxyphenyl)-3-methoxy-salicylaldimine (H2L), an ONO type tridentate ligand. The complexes of Cr(III), Fe(II), Fe(III), Co(II), Ni(II), Cu(II), and Zn(II) were prepared and characterized using various analytical techniques including elemental analysis, magnetic moment measurements, molar conductivity, thermogravimetric analysis (TGA), nuclear magnetic resonance (NMR), infrared (IR), ultraviolet-visible (UV-vis), and electrospray ionization-mass spectrometry (ESI-MS). The research revealed that all complexes, except for [Zn(L)(H2O)2], are paramagnetic and mostly adopt octahedral geometries, with the exception of Zn(II) and Fe(III) which exhibit five coordination geometries and Cu(II) which has a four-coordinated dimeric structure with acetato bridging. The antimicrobial activities of these complexes were tested against six bacterial strains and Candida albicans as a fungal strain, with Ni(II) and Co(II) complexes showing significant selective activity against S. epidermidis and C. albicans, and the Cr(III) complex displaying antibacterial activity against S. epidermidis, while the Zn(II) complex showed antifungal activity against C. albicans. The ligand itself did not exhibit any antimicrobial activity.

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