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33797-51-2 - (N,N-Dimethyl)methyleneammonium iodide, 97% - N,N-Dimethylmethyleneiminium iodide - Eschenmoser's iodide salt - A15146 - Alfa Aesar

A15146 (N,N-Dimethyl)methyleneammonium iodide, 97%

Numéro de CAS
33797-51-2
Synonymes
N,N-Dimethylmethyleneiminium iodide
Eschenmoser's iodide salt

Conditionnement Prix ($) Quantité Disponibilité
10g 69,30
50g 230,00
250g 1048,00
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(N,N-Dimethyl)methyleneammonium iodide, 97%

MDL
MFCD00011810
EINECS
251-680-2

Propriétés chimiques

Formule
C3H8IN
Poids moleculaire
185.01
Point de fusion
ca 240° dec.
Sensibilité
Moisture & Light Sensitive
Solubilité
Soluble in dimethylformamide. Partially soluble in acetonitrile, tetrahydrofuran and dichloromethane.

Applications

(N,N-Dimethyl)methyleneammonium iodide is a useful reagent for many synthetic applications like aminomethylation. It is also essential for the conversion of ketones to α, β-unsaturated enones. It is utilized to prepare derivatives of the type RCH2N(CH3)2. It is extensively used in medicines like painkillers and sedatives- Tramadol hydrochloride intermediate viz. 2-dimethylamine methylcyclohexanone. It is also employed in reactive dyes, synthesized spices. It plays an essential role in Mannich reactions.

Notes

Moisture and light sensitive. Store in a cool place. Keep the container tightly closed in a dry and well-ventilated place.

Références bibliographiques

Crystalline salt of the Mannich intermediate, used by Eschenmoser to introduce a dimethylaminomethyl group into the corrin nucleus: Angew. Chem. Int. Ed., 10, 330 (1971). Enolates of ketones, esters and lactones give the Mannich bases from which the ɑ-methylene derivatives can be prepared by quaternization and elimination: Tetrahedron Lett., 1621 (1977). Malonate esters are converted to ɑ-substituted acrylates: J. Am. Chem. Soc., 104, 6787 (1982); 108, 8068 (1986); J. Chem. Soc., Chem. Commun., 480 (1989).

The dimethylaminomethylenation of phenols gives high yields and shows a high ortho-regioselectivity: Synthesis, 906 (1983). Indoles are converted almost quantitatively to their 3-dimethylaminomethyl derivatives: Heterocycles, 14, 55 (1980).

/n

Cesario, C.; Miller, M. J. Palladium(0)/indium iodide-mediated allylations of electrophiles generated from the hydrolysis of Eschenmoser’s salt: one-pot preparation of diverse carbocyclic scaffolds. Tetrahedron Lett. 2010, 51 (23), 3050-3052.

Yamada, K.; Masaki, K.; Hagimoto, Y.; Kamiya, S.; Kunishima, M. A new method using 2-chloro-4,6-dimethoxy-1,3,5-triazine for facile elimination of dimethylamino group in Eschenmoser’s methylenation for synthesis of alpha,beta-unsaturated esters. Tetrahedron Lett. 2013, 54 (13), 1758-1760.

Mentions de danger et de prudence du SGH

Mentions de danger (UE): H315-H319-H335

Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.

Mentions de prudence: P261-P280a-P305+P351+P338-P304+P340-P405-P501a

Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves and eye/face protection. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Autres références

Merck
14,3251
Beilstein
3594966
Code tarifaire harmonisé
2925.29
TSCA
No

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