Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride

ISSN:
1573-9171
Keywords:
X-ray crystallographic analysis ; heterylamidine ; N-(1,2,4-triazol-5-yl)benzamidine ; N-(1,2,4-triazol-5-yl)benzamidine hydrochloride
Source:
Springer Online Journal Archives 1860-2000
Topics:
Chemistry and Pharmacology
Notes:
Abstract The crystal and molecular structures of N-(1,2,4-triazol-5-yl)benzamidine (1) and its hydrochloride (2) were determined by x-ray crystallography. In compound 1 both independent molecules are Z isomers of the anidine substituted in the imino group and 5-substituted 1H-1,2,4-triazoles. In the crystal the molecules of compound 1 are linked into a stable dimer by intermolecular hydrogen bonds. An undissociated HCl molecule was unexpectedly found in the structure of compound 2, while the structure of the base corresponded to the Z isomer of the amidine substituted in the amino group and to 2H-1,2,4-triazole substituted at position 5. The structures of compounds 1 and 2 are stabilized by an intramolecular hydrogen bond. The HCl molecule participates in the formation of intermolecular hydrogen bonds in compound 2.
Type of Medium:
Electronic Resource
URL:
_version_ 1798297499013742594
autor Kurella, M. G.
Vorontsova, L. G.
Amamchyan, A. R.
Dorokhov, V. A.
autorsonst Kurella, M. G.
Vorontsova, L. G.
Amamchyan, A. R.
Dorokhov, V. A.
book_url http://dx.doi.org/10.1007/BF00866590
datenlieferant nat_lic_papers
hauptsatz hsatz_simple
identnr NLM192206842
iqvoc_descriptor_keyword iqvoc_00000708:analysis
issn 1573-9171
journal_name Russian chemical bulletin
materialart 1
notes Abstract The crystal and molecular structures of N-(1,2,4-triazol-5-yl)benzamidine (1) and its hydrochloride (2) were determined by x-ray crystallography. In compound 1 both independent molecules are Z isomers of the anidine substituted in the imino group and 5-substituted 1H-1,2,4-triazoles. In the crystal the molecules of compound 1 are linked into a stable dimer by intermolecular hydrogen bonds. An undissociated HCl molecule was unexpectedly found in the structure of compound 2, while the structure of the base corresponded to the Z isomer of the amidine substituted in the amino group and to 2H-1,2,4-triazole substituted at position 5. The structures of compounds 1 and 2 are stabilized by an intramolecular hydrogen bond. The HCl molecule participates in the formation of intermolecular hydrogen bonds in compound 2.
package_name Springer
publikationsjahr_anzeige 1992
publikationsjahr_facette 1992
publikationsjahr_intervall 8009:1990-1994
publikationsjahr_sort 1992
publisher Springer
reference 41 (1992), S. 1079-1083
schlagwort X-ray crystallographic analysis
heterylamidine
N-(1,2,4-triazol-5-yl)benzamidine
N-(1,2,4-triazol-5-yl)benzamidine hydrochloride
search_space articles
shingle_author_1 Kurella, M. G.
Vorontsova, L. G.
Amamchyan, A. R.
Dorokhov, V. A.
shingle_author_2 Kurella, M. G.
Vorontsova, L. G.
Amamchyan, A. R.
Dorokhov, V. A.
shingle_author_3 Kurella, M. G.
Vorontsova, L. G.
Amamchyan, A. R.
Dorokhov, V. A.
shingle_author_4 Kurella, M. G.
Vorontsova, L. G.
Amamchyan, A. R.
Dorokhov, V. A.
shingle_catch_all_1 Kurella, M. G.
Vorontsova, L. G.
Amamchyan, A. R.
Dorokhov, V. A.
Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride
X-ray crystallographic analysis
heterylamidine
N-(1,2,4-triazol-5-yl)benzamidine
N-(1,2,4-triazol-5-yl)benzamidine hydrochloride
X-ray crystallographic analysis
heterylamidine
N-(1,2,4-triazol-5-yl)benzamidine
N-(1,2,4-triazol-5-yl)benzamidine hydrochloride
Abstract The crystal and molecular structures of N-(1,2,4-triazol-5-yl)benzamidine (1) and its hydrochloride (2) were determined by x-ray crystallography. In compound 1 both independent molecules are Z isomers of the anidine substituted in the imino group and 5-substituted 1H-1,2,4-triazoles. In the crystal the molecules of compound 1 are linked into a stable dimer by intermolecular hydrogen bonds. An undissociated HCl molecule was unexpectedly found in the structure of compound 2, while the structure of the base corresponded to the Z isomer of the amidine substituted in the amino group and to 2H-1,2,4-triazole substituted at position 5. The structures of compounds 1 and 2 are stabilized by an intramolecular hydrogen bond. The HCl molecule participates in the formation of intermolecular hydrogen bonds in compound 2.
1573-9171
15739171
Springer
shingle_catch_all_2 Kurella, M. G.
Vorontsova, L. G.
Amamchyan, A. R.
Dorokhov, V. A.
Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride
X-ray crystallographic analysis
heterylamidine
N-(1,2,4-triazol-5-yl)benzamidine
N-(1,2,4-triazol-5-yl)benzamidine hydrochloride
X-ray crystallographic analysis
heterylamidine
N-(1,2,4-triazol-5-yl)benzamidine
N-(1,2,4-triazol-5-yl)benzamidine hydrochloride
Abstract The crystal and molecular structures of N-(1,2,4-triazol-5-yl)benzamidine (1) and its hydrochloride (2) were determined by x-ray crystallography. In compound 1 both independent molecules are Z isomers of the anidine substituted in the imino group and 5-substituted 1H-1,2,4-triazoles. In the crystal the molecules of compound 1 are linked into a stable dimer by intermolecular hydrogen bonds. An undissociated HCl molecule was unexpectedly found in the structure of compound 2, while the structure of the base corresponded to the Z isomer of the amidine substituted in the amino group and to 2H-1,2,4-triazole substituted at position 5. The structures of compounds 1 and 2 are stabilized by an intramolecular hydrogen bond. The HCl molecule participates in the formation of intermolecular hydrogen bonds in compound 2.
1573-9171
15739171
Springer
shingle_catch_all_3 Kurella, M. G.
Vorontsova, L. G.
Amamchyan, A. R.
Dorokhov, V. A.
Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride
X-ray crystallographic analysis
heterylamidine
N-(1,2,4-triazol-5-yl)benzamidine
N-(1,2,4-triazol-5-yl)benzamidine hydrochloride
X-ray crystallographic analysis
heterylamidine
N-(1,2,4-triazol-5-yl)benzamidine
N-(1,2,4-triazol-5-yl)benzamidine hydrochloride
Abstract The crystal and molecular structures of N-(1,2,4-triazol-5-yl)benzamidine (1) and its hydrochloride (2) were determined by x-ray crystallography. In compound 1 both independent molecules are Z isomers of the anidine substituted in the imino group and 5-substituted 1H-1,2,4-triazoles. In the crystal the molecules of compound 1 are linked into a stable dimer by intermolecular hydrogen bonds. An undissociated HCl molecule was unexpectedly found in the structure of compound 2, while the structure of the base corresponded to the Z isomer of the amidine substituted in the amino group and to 2H-1,2,4-triazole substituted at position 5. The structures of compounds 1 and 2 are stabilized by an intramolecular hydrogen bond. The HCl molecule participates in the formation of intermolecular hydrogen bonds in compound 2.
1573-9171
15739171
Springer
shingle_catch_all_4 Kurella, M. G.
Vorontsova, L. G.
Amamchyan, A. R.
Dorokhov, V. A.
Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride
X-ray crystallographic analysis
heterylamidine
N-(1,2,4-triazol-5-yl)benzamidine
N-(1,2,4-triazol-5-yl)benzamidine hydrochloride
X-ray crystallographic analysis
heterylamidine
N-(1,2,4-triazol-5-yl)benzamidine
N-(1,2,4-triazol-5-yl)benzamidine hydrochloride
Abstract The crystal and molecular structures of N-(1,2,4-triazol-5-yl)benzamidine (1) and its hydrochloride (2) were determined by x-ray crystallography. In compound 1 both independent molecules are Z isomers of the anidine substituted in the imino group and 5-substituted 1H-1,2,4-triazoles. In the crystal the molecules of compound 1 are linked into a stable dimer by intermolecular hydrogen bonds. An undissociated HCl molecule was unexpectedly found in the structure of compound 2, while the structure of the base corresponded to the Z isomer of the amidine substituted in the amino group and to 2H-1,2,4-triazole substituted at position 5. The structures of compounds 1 and 2 are stabilized by an intramolecular hydrogen bond. The HCl molecule participates in the formation of intermolecular hydrogen bonds in compound 2.
1573-9171
15739171
Springer
shingle_title_1 Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride
shingle_title_2 Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride
shingle_title_3 Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride
shingle_title_4 Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride
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source_archive Springer Online Journal Archives 1860-2000
timestamp 2024-05-06T10:08:57.675Z
titel Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride
titel_suche Some features of the crystal and molecular structure of N-(1,2,4-triazol-5-yl)benzamidine and its hydrochloride
topic V
uid nat_lic_papers_NLM192206842