4-Hydroxyethyl-4-methylmorpholinium chloride

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منابع مشابه

A racemization test in peptide synthesis using 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM).

Racemization of the C-terminal amino acid (Ala) has been studied in various solvents during coupling between 4-methoxybenzyloxycarbonyl (Z(OMe))-Gly-L-Ala-OH and phenylalanine benzyl ester (H-Phe-OBzl) with 4-(4,6-dimethoxy-1,3,5-thiazin-2-yl)-4-methylmorpholinium chloride (DMT-MM). The reaction occurred without substantial racemization in AcOEt, tetrahydrofuran (THF), N,N-dimethylformamide (DM...

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4-Allyl-4-ethyl­morpholinium chloride

In the title molecular salt, C(9)H(18)NO(+)·Cl(-), the morpholine ring adopts a chair conformation. In the crystal structure, intra-molecular C-H⋯Cl bonds occur and inter-molecular C-H⋯O and C-H⋯Cl hydrogen bonds link the mol-ecules.

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4-(4-Nitro­benzene­sulfonamido)pyri­dinium chloride

In the title compound, C(11)H(10)N(3)O(4)S(+)·Cl(-), the benzene ring makes an angle of 89.2 (1)° with the pyridinium ring. The dihedral angle between the nitro group and the benzene ring is 15.7 (1)°. The crystal structure is stabilized by N-H⋯Cl hydrogen bonds.

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4-Hydroxy­ethyl-4-methyl­morpholinium chloride

In the title compound, C(7)H(16)NO(2) (+)·Cl(-), the asymmetric unit consists of two cation-anion pairs, in which the ion pairs are inter-connected by weak C-H⋯Cl hydrogen bonds. Each cation forms a network of weak C-H⋯Cl hydrogen bonds to surrounding chloride ions. The morpholine ring is in a chair conformation. The crystal structure is consolidated by O-H⋯Cl, C-H⋯Cl and C-H⋯O inter-molecular ...

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4-(4-Methoxy­phen­yl)piperazin-1-ium chloride

In the title compound, C(11)H(17)N(2)O(+)·Cl(-), the dihedral angle between the benzene ring and the basal plane of piperazine ring is 39.20 (8)°. In the crystal, intermolecular N-H⋯Cl hydrogen bonds occur. There is also a C-H⋯π inter-action between the benzene rings.

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ژورنال

عنوان ژورنال: Acta Crystallographica Section E Structure Reports Online

سال: 2008

ISSN: 1600-5368

DOI: 10.1107/s1600536808030195