References of N,N-dimethyl-N'-pyridin-2-yl-N'-(thiophen-3-ylmethyl)ethane-1,2-diamine
Title: Thenyldiamine
CAS Registry Number: 91-79-2
CAS Name: N,N-Dimethyl-
N¢-2-pyridinyl-
N¢-(3-thienylmethyl)-1,2-ethanediamine
Synonyms: 2-[(2-dimethylaminoethyl)-3-thenylamino]pyridine;
N,N-dimethyl-
N¢-(a-pyridyl)-
N¢-(3-methylthienyl)ethylenediamine;
N-(a-pyridyl)-
N-(b-thenyl)-
N¢,N¢-dimethylethylenediamine;
N-(2-dimethylaminoethyl)-
N-2-pyridyl-3-thenylamine; dethylandiamine
Manufacturers' Codes: Win-2848
Trademarks: Thenfadil (Winthrop)
Molecular Formula: C14H19N3S
Molecular Weight: 261.39
Percent Composition: C 64.33%, H 7.33%, N 16.08%, S 12.27%
Literature References: Prepn: Campaigne, LeSuer,
J. Am. Chem. Soc. 71, 333 (1949). Toxicity study: Hoppe, Lands,
J. Pharmacol. Exp. Ther. 97, 371 (1949).
Properties: Free base, liquid. bp1.0 169-172°.
nD20 1.5915.
Boiling point: bp1.0 169-172°
Index of refraction: nD20 1.5915
Derivative Type: Hydrochloride
Molecular Formula: C14H19N3S.HCl
Molecular Weight: 297.85
Percent Composition: C 56.45%, H 6.77%, N 14.11%, S 10.77%, Cl 11.90%
Properties: Crystals from methanol, mp 169.5-170°. Bitter taste. Sol in water up to 20%. Slightly sol in alc. pH of 1% aq soln 6.5. LD50 orally in rats: 525 mg/kg (Hoppe, Lands).
Melting point: mp 169.5-170°
Toxicity data: LD50 orally in rats: 525 mg/kg (Hoppe, Lands)
Therap-Cat: Hydrochloride as antihistaminic.
Keywords: Antihistaminic; Ethylenediamine Derivatives.