Dibromido[N-propyl-N′-(2-pyridylmethylidene)ethane-1,2-diamine]zinc(II)
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چکیده
منابع مشابه
Methyl-n-propyl ether.
ME T H Y L N P R O P Y L ETHER is an isomer of di-ethyl ether and possesses the formula CHs-O(CHI)J-CHJ. The physical properties of the two drugs are similar, and the vapour pressure curve of methyl-n-propyl ether is such that it may be used in the Oxford Vaporizer No. 1 without any alteration in the calibration of the instrument (see Figure). Methyl-n-propyl ether has a very unpleasant pungent...
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Two independent mol-ecules comprise the asymmetric unit in the title thio-carbamide derivative, C(10)H(13)NOS. These differ in the relative orientations of terminal ethyl groups [C-C-C-O torsion angles = -66.95 (13) and 55.92 (13)°, respectively]. The phenyl ring is twisted out of the plane of the central residue [C(q)-N-C(ph)-C(ph) = -146.20 (12) and -144.15 (12)°, respectively; q = quaternary...
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Before the preliminary account of the present work (Grenby & Young, 1959) there appears to have been no report of the isolation of a biosynthetic alkylmercapturic acid. Evidence had been obtained, however, which suggested that alkylmercapturic acids could probably be isolated from the urine of animals which had been dosed with certain alkylating agents. Roberts & Warwick (1957, 1958), by means ...
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In the title compound, C(12)H(14)N(2)O(2), the benzene ring and imidazole ring are almost coplanar, making a dihedral angle of 2.47 (14)°. Inter-molecular O-H⋯N, N-H⋯O and C-H⋯O hydrogen bonds stabilize the crystal structure.
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The present study was designed to evaluate the antidepressant potential of 5-HT3 receptor antagonist N-n-propyl-3-ethoxyquinoxaline-2-carboxamide (6n). The compound '6n' with optimum log P and pA 2 value identified from a series of compounds synthesized in our laboratory was subjected to forced Swim Test (FST) (1, 2, and 4 mg/kg, i.p) and Tail Suspension Test (TST) (1, 2, and 4 mg/kg, i.p.). Th...
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ژورنال
عنوان ژورنال: Acta Crystallographica Section E Structure Reports Online
سال: 2008
ISSN: 1600-5368
DOI: 10.1107/s1600536808023660