Detail of "6583-06-8"

Reference

4-Hydroxy-7-aminobenzo-2,1,3-thiadiazole

4-Hydroxy-7-aminobenzo-2,1,3-thiadiazole. Pesin, V. G.; Belen'kaya, I. A.; Dubovskova, L. P. (USSR ). U.S.S.R. SU 545643 5 Feb 1977 From: Otkrytiya, Izobret., Prom. Obraztsy, Tovarnye Znaki 1977, 54(5), 91. (Russian). (Union of Soviet Socialist Republics). CODEN: URXXAF. CLASS: IC: C07D285-14. APPLICATION: SU 75-2151723 20 Jun 1975.There are some commonly used reagents with their cas registry numbers 1753-27-1 and 6583-06-8 in this article. DOCUMENT TYPE: Patent CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Redn. of 4-nitrobenzo-2,1,3-thiadiazole with an alc. soln. of NH3 and H2S at room temp. followed by refluxing the reaction mass with concd. HCl gave the title compd. .

Microbiological reduction of 4-nitrobenzo-2,1,3-thiadiazole

Microbiological reduction of 4-nitrobenzo-2,1,3-thiadiazole. Davidenko, T. I.; Kotlyar, I. I.; Belen'kaya, I. A.; Andronati, S. A. (Fiz.-Khim. Inst., Odessa, USSR). Deposited Doc., VINITI 5405-82, 7 pp. Avail. VINITI (Russian) 1982. DOCUMENT TYPE: Report CA Section: 16 (Fermentation and Bioindustrial Chemistry) Section cross-reference(s): 10, 59 Degrdn. of 4-nitrobenzo-2,1,3-thiadiazole [6583-06-8] by Escherichia coli yielded a product, which by physicochem. properties and UV, IR, and mass spectra was identified as 4-aminobenzo-2,1,3-thiadiazole [767-64-6].There are some commonly used reagents with their cas registry numbers 767-64-6 and 6583-06-8 in this article. The yield of the latter compd. was highest when the concn. of the former one was 100-300 mg/50 mg bacterial cells (on wet-wt. basis). .