Detail of "26116-12-1"

CAS Number:
26116-12-1
Name:
2-Pyrrolidinemethanamine,1-ethyl-
Superlist Name:
2-(Aminomethyl)-N-ethylpyrrolidine
Molecular Structure:
Formula:
C₇H₁₆N₂
Molecular Weight:
128.22
Synonyms:
Pyrrolidine,2-(aminomethyl)-1-ethyl- (7CI,8CI);(1-Ethyl-2-pyrrolidinyl)methylamine;1-(1-Ethylpyrrolidin-2-yl)methanamine;1-Ethyl-2-(aminomethyl)pyrrolidine;1-Ethyl-2-pyrrolidinemethylamine;2-(Aminomethyl)-1-ethylpyrrolidine;N-Ethyl-2-(aminomethyl)pyrrolidine;
EINECS:
247-466-3
Density:
0.902 g/cm³
Boiling Point:
161.901 °C at 760 mmHg
Flash Point:
60.556 °C
Appearance:
clear yellow liquid
Hazard Symbols:
Xi,Xn
Risk Codes:
36/37/38-20/21/22
Safety:
26-36 Details
Transport Information:
UN 1993 3/PG 3

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O-(4-Chlorophenoxyisobutyryl)salicylic acids: O-(4-Chlorophenoxyisobutyryl)salicylic acids. Dufour, Claude (Societe d'Etudes et Applications Chimiques, Fr.). Ger. Offen. DE 2612321 7 Oct 1976, 29 pp. (German). (Germany). CODEN: GWXXBX. CLASS: IC: C07C069-67. PRIORITY: FR 75-9195 24 Mar 1975. 109-89-7 and 26116-12-1 are also in the experiment. DOCUMENT TYPE: Patent CA Section: 25 (Noncondensed Aromatic Compounds) 2-(4-ClC6H4OCMe2CO2)C6H4CO2H (I), as well as its salts, esters, and amides were prepd. from salicylic acid (II). Thus, II and 4-ClC6H4OCMe2COCl were refluxed in CHCl3 and Et3N to give I, which was converted into its esters and amides via the acid chloride. I and its derivs. are useful as antipyretics, anticholesteremics, and antiinflammatory agents. .

Enamines: Enamines. Bulteau, Gerard; Acher, Jacques; Monier, Jean C. (Societe d'Etudes Scientifiques et Industrielles de I'lle-de-France, Fr.). Ger. Offen. DE 2623076 30 Dec 1976, 6 pp.Some commonly used reagents like 62039-46-7 and 26116-12-1 are used in this experiment. (German). (Germany). CODEN: GWXXBX. CLASS: IC: C07D207-08. PRIORITY: FR 75-18344 12 Jun 1975. DOCUMENT TYPE: Patent CA Section: 27 (Heterocyclic Compounds (One Hetero Atom)) Reaction of 2-(aminomethyl)-1-ethylpyrrolidine with MeCOCH2CO2Me in presence of HCl at 20-54.degree. gives after cooling and 1 h stirring at room temp. 81.1% I which when dissolved in Me2CO and treated with alc. HCl gives 95.2% I.HCl. .