Welcome to LookChem.com Sign In|Join Free
  • or
Ortho-ferrocenyl benzoyl ethyl ester is a complex organic compound with the chemical formula C19H18FeO3. It is a derivative of benzoic acid, featuring a ferrocene group attached to the ortho position of the benzene ring. Ferrocene is an organometallic compound consisting of a cyclopentadienyl anion and a central iron atom. The molecule also contains an ethyl ester group, which is formed by the esterification of benzoic acid with ethanol. ortho-ferrocenyl benzoyl ethyl ester is known for its unique chemical properties and potential applications in various fields, such as pharmaceuticals, materials science, and catalysis. Due to its complex structure and the presence of a metal center, ortho-ferrocenyl benzoyl ethyl ester exhibits interesting electronic and steric properties, making it a subject of interest for researchers in organometallic chemistry.

1294-29-7

Post Buying Request

1294-29-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1294-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1294-29-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,9 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1294-29:
(6*1)+(5*2)+(4*9)+(3*4)+(2*2)+(1*9)=77
77 % 10 = 7
So 1294-29-7 is a valid CAS Registry Number.

1294-29-7Downstream Products

1294-29-7Relevant academic research and scientific papers

N-ortho-Ferrocenyl benzoyl dipeptide esters: Synthesis, structural characterization and in vitro anti-cancer activity of N-{ortho-(ferrocenyl)benzoyl}-glycine-l-alanine ethyl ester and N-{ortho-(ferrocenyl)benzoyl}-l-alanine-glycine ethyl ester

Corry, Alan J.,Goel, Alok,Alley, Steven R.,Kelly, Paula N.,O'Sullivan, Dermot,Savage, David,Kenny, Peter T.M.

, p. 1405 - 1410 (2007)

N-ortho-ferrocenyl benzoyl dipeptide esters 2-6 were prepared by coupling ortho-ferrocenyl benzoic acid 1 to the dipeptide ethyl esters GlyGly(OEt) (2), GlyAla(OEt) (3), GlyPhe(OEt) (4), AlaGly(OEt) (5) and AlaPhe(OEt) (6). The compounds were fully characterized by a range of NMR spectroscopic techniques, mass spectrometry and cyclic voltammetry. The cytotoxicity of 3 and 5 towards lung cancer cells has been determined.

Synthesis, characterization and in vitro anti-cancer activity of N-(ferrocenyl)benzoyl tri- and tetrapeptide esters

Corry, Alan J.,Mooney, áine,O'Sullivan, Dermot,Kenny, Peter T.M.

, p. 2957 - 2961 (2009/09/26)

N-ortho, N-meta and N-para-(ferrocenyl)benzoyl tri- and tetrapeptide esters (2-7) were prepared by coupling ortho, meta and para-ferrocenyl benzoic acids to the tri- and tetrapeptide ethyl esters of GlyGlyGly(OEt) and GlyGlyGlyGly(OEt) in the presence of

The synthesis and structural characterization of N-ortho-ferrocenyl benzoyl amino acid esters. The X-ray crystal structure of N-{ortho-(ferrocenyl)benzoyl} -l-phenylalanine ethyl ester

Savage, David,Malone, Gwen,Alley, Steven R.,Gallagher, John F.,Goel, Alok,Kelly, Paula N.,Mueller-Bunz, Helge,Kenny, Peter T.M.

, p. 463 - 469 (2007/10/03)

A series of N-ortho-ferrocenyl benzoyl amino acid ethyl esters 3-9 have been prepared by coupling ortho-ferrocenyl benzoic acid 2 to the amino acid ethyl esters of glycine, l-alanine, l-leucine, l-phenylalanine, β-alanine, 4-aminobutyric acid and (±)-2-aminobutyric acid using the conventional 1,3-dicyclohexylcarbodiimide, 1-hydroxybenzotriazole protocol. The compounds were fully characterized by a range of NMR spectroscopic techniques and by mass spectrometry (MALDI-MS, ESI-MS). The X-ray crystal structure of the l-phenylalanine derivative 6 has been determined.

Bis(ferrocenyl)mercury as a source of ferrocenyl moiety in Pd-catalyzed reactions of carbon-carbon bond formation

Beletskaya, Irina P.,Tsvetkov, Alexei V.,Latyshev, Gennadij V.,Tafeenko, Victor A.,Lukashev, Nikolai V.

, p. 653 - 663 (2007/10/03)

The application of bis(ferrocenyl)mercury as a source of ferrocenyl group in Pd-catalyzed reactions with aryl halides, acid chlorides and electrophilic alkynes has been demonstrated. The formation of dimethyl-(Z)-2,3-di(ferrocenyl)-2-butenedioate in Pd-catalyzed addition of bis(ferrocenyl)mercury to dimethylacetylenedicarboxylate has been confirmed by X-ray analysis.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1294-29-7