Home > Name List By n > N,N-Dimethylmethyleneiminium iodide Germany

CAS No 33797-51-2 , N,N-Dimethylmethyleneiminium iodide Search by region : Germany

  • Name: N,N-Dimethylmethyleneiminium iodide
  • Synonyms: N,N-Dimethylmethyleneiminium iodide;N,N-Dimethylmethyleneiminium iodide; Dimethyl methyleneimmonium iodide; Eschenmoser salt;Dimethyl methyleneammonium iodide~Eschenmosers iodide salt;
  • CAS Registry Number:
  • Flash Point: °C
  • Boiling Point: °Cat760mmHg
  • Density: g/cm3
  • Safety Statements: R36/37/38
  • Hazard Symbols: Xi: Irritant;
  • Flash Point: °C
  • EINECS: 251-680-2
  • Molecular Weight: 185.01
  • InChI: InChI=1/C3H8N.HI/c1-4(2)3;/h1H2,2-3H3;1H/q+1;/p-1
  • Risk Statements: S26;S36
  • Molecular Formula: C3H8N.I
  • Molecular Structure:CAS No:33797-51-2 N,N-Dimethylmethyleneiminium iodide

Related products

Select to

33797-51-2 (N,N-Dimethyl)methyleneammonium iodide; 97%

  • (N,N-Dimethyl)methyleneammonium iodide; 97%
  • Germany ABCR GmbH & Co KG [Manufacturer]
  • Tel: +49 721 95061-0
  • Fax: +49 721 95061-80
  • Address: Im Schlehert 10
    76187 Karlsruhe
    Germany null,nullGermany
Contact Supplier

33797-51-2 N,N-Dimethylmethyleneammonium iodide

  • N,N-Dimethylmethyleneammonium iodide
  • Germany CHEMOS GmbH [Manufacturer]
  • Tel: 0049 9402/9336 0
  • Fax: 0049 9402/9336 13
  • Address: CHEMOS GmbH
    Werner-von-Siemensstr. 3
    93128 Regenstauf
    Germany null,nullGermany
Contact Supplier

Select to

1/1
References of N,N-Dimethylmethyleneiminium iodide
Title: Dimethyl(methylene)ammonium Iodide
CAS Registry Number: 33797-51-2
CAS Name: N-Methyl-N-methylenemethanaminium iodide
Synonyms: Eschenmoser's salt
Molecular Formula: C3H8IN
Molecular Weight: 185.01
Percent Composition: C 19.48%, H 4.36%, I 68.59%, N 7.57%
Line Formula: H2C=N(CH3)2I
Literature References: Mannich type intermediate originally developed to introduce methyl groups into corrin chromophore. Prepn from trimethylamine and diiodomethane: J. Schreiber et al., Angew. Chem. Int. Ed. 10, 330 (1971); from N,N,N￠,N￠-tetramethylmethylenediamine: T. A. Bryson et al., J. Org. Chem. 45, 524 (1980). Used in prepn of Mannich bases: J. Hooz, J. N. Bridson, J. Am. Chem. Soc. 95, 602 (1973). In functionalization of indoles: A. P. Kozikowski, H. Isida, Heterocycles 14, 55 (1980). In prepn of a-methylene carbonyls: J. L. Roberts et al., Tetrahedron Lett. 1977, 1621; of terminal olefins: eidem, ibid. 1299.
Properties: Colorless crystals from tetrahydrothiophene dioxide, dec ~240°. Sublimes at 120° at 0.05 torr.
Use: In organic synthesis.