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ChemInform Abstract: A 1,2,3‐THIADIAZOLE‐1,2,3‐THIADIAZOLE REARRANGEMENT
Chemischer Informationsdienst, 1983AbstractAus den Thiadiazolen (I) und (IV) entstehen unter Umlagerung die Diazoverbindungen (II) bzw. (V).
G. L'ABBE, J.‐P. DEKERK, M. DEKETELE
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Acta Crystallographica Section C Crystal Structure Communications, 1990
C 2 H 2 N 6 S cristallise dans P2 1 /a avec a=9,018, b=10,975, c=5,5305A, β=99,17°, Z=4; affinement jusqu'a R=0,058. Le groupement azido adopte une conformation transetendue. L'atome N de l'amine, type sp 2 , participe aux deux liaisons hydrogene intermoleculaires, de 3,264 et 3 ...
K. Yamaguchi, A. Ohsawa, C. Kawabata
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C 2 H 2 N 6 S cristallise dans P2 1 /a avec a=9,018, b=10,975, c=5,5305A, β=99,17°, Z=4; affinement jusqu'a R=0,058. Le groupement azido adopte une conformation transetendue. L'atome N de l'amine, type sp 2 , participe aux deux liaisons hydrogene intermoleculaires, de 3,264 et 3 ...
K. Yamaguchi, A. Ohsawa, C. Kawabata
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2015
[288-48-2 C2H2N2S (MW 86.12) InChI = 1S/C2H2N2S/c1-2-5-4-3-1/h1-2H InChIKey = UGUHFDPGDQDVGX-UHFFFAOYSA-N (heteroaromatic compound, precursor to thiirenes) Physical Data: bp 98 °C, mp −28 °C. Alternate Name: 2,3-diazathiophene. Handling: compound known to possess potent biological activities in humans.
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[288-48-2 C2H2N2S (MW 86.12) InChI = 1S/C2H2N2S/c1-2-5-4-3-1/h1-2H InChIKey = UGUHFDPGDQDVGX-UHFFFAOYSA-N (heteroaromatic compound, precursor to thiirenes) Physical Data: bp 98 °C, mp −28 °C. Alternate Name: 2,3-diazathiophene. Handling: compound known to possess potent biological activities in humans.
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2015
[288-92-6] C2H2N2S (MW 86.11) InChI = 1S/C2H2N2S/c1-3-2-5-4-1/h1-2H InChIKey = YGTAZGSLCXNBQL-UHFFFAOYSA-N (prepared from 5-bromo-1,2,4-thiadiazole) Alternate Name(s): 1-thia-2,4-diazacyclopentadiene; 2,4-diazathiophene. Physical Data: mp −33 to −35 °C, bp753 120.7–121.2 °C, d 1.3298 g mL−1 at 20 °C, 1.5316; λmax 229 nm ...
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[288-92-6] C2H2N2S (MW 86.11) InChI = 1S/C2H2N2S/c1-3-2-5-4-1/h1-2H InChIKey = YGTAZGSLCXNBQL-UHFFFAOYSA-N (prepared from 5-bromo-1,2,4-thiadiazole) Alternate Name(s): 1-thia-2,4-diazacyclopentadiene; 2,4-diazathiophene. Physical Data: mp −33 to −35 °C, bp753 120.7–121.2 °C, d 1.3298 g mL−1 at 20 °C, 1.5316; λmax 229 nm ...
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1965
Publisher Summary 1,2, 4-thiadiazole derivatives have recently found important uses and have attained industrial and economic importance. The syntheses of 1,2,4-thiadiazoles are classified according to the nature of the fragments, from which the heterocyclic ring is built.
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Publisher Summary 1,2, 4-thiadiazole derivatives have recently found important uses and have attained industrial and economic importance. The syntheses of 1,2,4-thiadiazoles are classified according to the nature of the fragments, from which the heterocyclic ring is built.
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2008
This chapter deals with new developments in the field of 1,2,4-thiadiazoles, covering the period 1996–2006, updating CHEC-II(1996). Developments in structure determination, especially X-ray structures, have been reported along with new reactions of both the fully aromatic and reduced ring systems. New examples of established methods of preparation have
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This chapter deals with new developments in the field of 1,2,4-thiadiazoles, covering the period 1996–2006, updating CHEC-II(1996). Developments in structure determination, especially X-ray structures, have been reported along with new reactions of both the fully aromatic and reduced ring systems. New examples of established methods of preparation have
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2008
This chapter deals with new developments in the field of 1,2,3-thiadiazoles updating the second edition covering the period 1996 to 2006. Developments in structure determination, especially X-ray structures, have been reported along with new reactions of both the fully aromatic and reduced ring systems.
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This chapter deals with new developments in the field of 1,2,3-thiadiazoles updating the second edition covering the period 1996 to 2006. Developments in structure determination, especially X-ray structures, have been reported along with new reactions of both the fully aromatic and reduced ring systems.
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