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Detail of "12086-40-7"

  • CAS Number:
  • 12086-40-7
  • Name:
  • Methanaminium,1-ferrocenyl-N,N,N-trimethyl-, iodide (1:1)

  • Molecular Structure:
  • Formula:
  • C14H20 Fe N . I
  • Molecular Weight:
  • 250.1017
  • Synonyms:
  • Ammonium,(ferrocenylmethyl)trimethyl-, iodide (8CI); Iron,cyclopentadienyl[[(dimethylamino)methyl]cyclopentadienyl]-, methiodide(6CI,7CI); Methanaminium, 1-ferrocenyl-N,N,N-trimethyl-, iodide (9CI);(Ferrocenylmethyl)trimethylammonium iodide; (N,N-Dimethylaminomethyl)ferrocenemethiodide; (Trimethylammoniomethyl)ferrocene iodide; N,N,N-Trimethyl(ferrocenylmethyl)ammoniumiodide; N-(Ferrocenylmethyl)trimethylammonium iodide;N-Ferrocenylmethyl-N,N,N-trimethylammonium iodide; NSC 20888
  • Density:
  • g/cm3
  • Melting Point:
  • 220°C (dec.)
  • Boiling Point:
  • °Cat760mmHg
  • Flash Point:
  • °C
  • Risk Codes:
  • R20/21/22;R36/37/38;

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CAS No.12086-40-7 Methanaminium,1-ferrocenyl-N,N,N-trimethyl-, iodide (1:1)

(Ferrocenylmethyl)trimethylammonium Iodide

Supplier:shanghai yinrui chemical technology co,.ltd [ China (Mainland)]

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CAS No.12086-40-7 (FERROCENYLMETHYL)TRIMETHYLAMMONIUM IODIDE

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Supplier:PARISH [ United States]

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Tel:(801) 226-2018

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CAS No.12086-40-7 Methanaminium,1-ferrocenyl-N,N,N-trimethyl-, iodide (1:1)

Supplier:Parish Chemical Company [ United States]

600Integral
600

Tel:801-226-2018

Address:PO Box 277

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Reference

a-Ferrocenylalkylation of polyfunctional nucleophilic compounds
a-Ferrocenylalkylation of polyfunctional nucleophilic compounds. Boev, V. I.; Betankourt, P.In this study, 12086-40-7 and 139750-30-4 are also used. M.; Popova, L. V.; Babin, V. N. (Lipetsk. Pedagog. Inst., Lipetsk, USSR). Zh. Obshch. Khim., 61(7), 1651-61 (Russian) 1991. CODEN: ZOKHA4. ISSN: 0044-460X. DOCUMENT TYPE: Journal CA Section: 29 (Organometallic and Organometalloidal Compounds) Reaction of FcCH(R)OH (Fc = ferrocenyl; R = H, Me, Ph) with polyfunctional nucleophiles, e.g., derivs. of benzimidazole, 2-mercaptothiazole, 2-methyl-8-mercaptoquinoline, and 2-methyl-6-(5-mercapto-1-tetrazolyl)benzothiazole, in a two-phase CH2Cl2-H2O system contg. HBF4 gave products of a-ferrocenylalkylation depending on the basicity of the nucleophiles, on their steric properties, and on the molar ratio of reactants. Mono- bis-, and tris (ferrocenylalkylation) products were obtained in high yields. E.g., reaction of 6-nitrobenzimidazole with 1 or 2 equiv FcCH2OH in CH2Cl2-H2O contg. HBF4 gave 71, 65% derivs. I (R = H, CH2Fc), resp. .
Ferrocenylmethylation of aniline: non-kinetic determination of a reaction mechanism
Ferrocenylmethylation of aniline: non-kinetic determination of a reaction mechanism. Lombardo, Anthony; Bieber, Theodore I. (Florida Atl. Univ., Boca Raton, FL 33431, USA). J. Chem.There are some reagents with their cas registry numbers 62-53-3 and 12086-40-7 are used in this study. Educ., 60(12), 1080-1 (English) 1983. CODEN: JCEDA8. ISSN: 0021-9584. DOCUMENT TYPE: Journal CA Section: 20 (History, Education, and Documentation) Expts. are described for the detn. of the reaction mechanism of the ferrocenylmethylation of aniline in a N atm. Products of the reaction are sepd. by column chromatog., identified by IR and NMR spectroscopy, and reaction mechanisms proposed. .
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