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CAS No 87-52-5 , 1-(1H-indol-3-yl)-N,N-dimethylmethanamine

  • Name: 1-(1H-indol-3-yl)-N,N-dimethylmethanamine
  • Synonyms: Donaxine; 87-52-5; Donaxin;1-(1H-indol-3-yl)-N,N-dimethylmethanamine; beta-Dimethylaminomethylindole;3-(Dimethylaminomethyl)indole; N,N-dimethyl-; 1H-Indole-3-methanamine; Gramin;
  • CAS Registry Number:
  • Melting Point: 131-139 ºC
  • Flash Point: 167 ºC
  • Boiling Point:
  • Density: 0.7692 g/cm3 (20 C)
  • Refractive index: 1.44 (20 C)
  • Safety Statements: R36:Irritatingtoeyes.;
  • Hazard Symbols: Xi:Irritant;
  • Flash Point: 167 ºC
  • EINECS: 201-749-8
  • Molecular Weight: 174.24226
  • InchiKey: OCDGBSUVYYVKQZ-UHFFFAOYSA-N
  • InChI: InChI=1S/C11H14N2/c1-13(2)8-9-7-12-11-6-4-3-5-10(9)11/h3-7,12H,8H2,1-2H3
  • Risk Statements: S26:Incaseofcontactwitheyes,rinseimmediatelywithplentyofwaterandseekmedicaladvice.;S46:Ifswallowed,seekmedicaladviceimmediatelyandshowthiscontainerorlabel.;
  • Molecular Formula: C11H14N2
  • Molecular Structure:CAS No:87-52-5 1-(1H-indol-3-yl)-N,N-dimethylmethanamine

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87-52-5 GRAMINE

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87-52-5 Gramine

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87-52-5 Donaxine

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87-52-5 3-(dimethylaminomethyl)indole

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References of 1-(1H-indol-3-yl)-N,N-dimethylmethanamine
Title: Gramine
CAS Registry Number: 87-52-5
CAS Name: N,N-Dimethyl-1H-indole-3-methanamine
Synonyms: 3-(dimethylaminomethyl)indole
Trademarks: Donaxine
Molecular Formula: C11H14N2
Molecular Weight: 174.24
Percent Composition: C 75.83%, H 8.10%, N 16.08%
Literature References: In chlorophyll-deficient mutants of barley: Euler et al., Z. Physiol. Chem. 217, 23 (1933). In the Asiatic reed Arundo donax L., Gramineae: Orechoff, Norkina, Ber. 68, 436 (1935). From Acer saccharinum L. (the Silver Maple) and A. rubrum L., Aceraceae: Pachter et al., J. Org. Chem. 24, 1285 (1959); Pachter, J. Am. Pharm. Assoc. Sci. Ed. 48, 670 (1959). Synthesis: Kühn, Stein, Ber. 70, 567 (1937). Biosynthesis from tryptophan in barley: Bowden, Marion, Can. J. Chem. 29, 1037 (1951); O'Donovan, Leete, J. Am. Chem. Soc. 85, 461 (1963); Gower, Leete, ibid. 3683; see also Gross et al., Tetrahedron Lett. 1971, 4047.
Properties: Shiny, flat needles or plates from acetone, mp 138-139°. Absorption spectrum: Kanakoa et al., Chem. Pharm. Bull. 8, 294 (1960). Sol in alcohol, ether, chloroform; slightly sol in cold acetone. Practically insol in petr ether, water.
Melting point: mp 138-139°
 
Derivative Type: Hydrochloride
Molecular Formula: C11H14N2.HCl
Molecular Weight: 210.70
Percent Composition: C 62.70%, H 7.18%, N 13.30%, Cl 16.83%
Properties: Crystals from ethanol + ether, dec 191°. Sol in water.
 
Derivative Type: Methiodide
Molecular Formula: C11H14N2.CH3I
Molecular Weight: 316.18
Percent Composition: C 45.58%, H 5.42%, N 8.86%, I 40.14%
Properties: Crystals from methanol + benzene, mp 168-169°. Sol in water: Geissman, Armen, J. Am. Chem. Soc. 74, 3916 (1952).
Melting point: mp 168-169°