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Bithionol | CAS:97-18-7
Bithionol
  • Name:Bithionol
  • CAS:97-18-7
  • Synonyms:2,2'-Thio-bis(4,6-dichlorophenol); Bis(2-hydroxy-3,5-dichlorophenyl) sulfide
  • Molecular Formula:C12H6Cl4O2S
  • Molecular Weight:356.05
  • EINESC:202-565-0

Description

Properties

Melting point 188 ºC
Density 1.61

Safety

Symbol(GHS) Xn
Hazard Codes R20/21/22
SDS/MSDS S36

SDS

Source SDS/MSDS Samples
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Synthetic Route
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Articles
Peer-Reviewed Papers
Chemoselective high-throughput purification mediated by solid-supported reagents: its application to the first 6, 9-disubstituted purine library synthesis.K Kim et al.Combinatorial chemistry & high throughput screening, 3(2), 125-129 (2000-05-02) Additive Pummerer reaction of 3,5-O-(di-tert-butyl)silylene-4-thiofuranoid glycal: a high-yield and beta-selective entry to 4'-thioribonucleosides.Kazuhiro Haraguchi et al.The Journal of organic chemistry, 74(6), 2616-2619 (2009-02-27) Synthesis and biological properties of 9-(trans-4-hydroxy-2-buten-1-yl)adenine and guanine: open-chain analogues of neplanocin A.S Phadtare et al.Journal of medicinal chemistry, 30(2), 437-440 (1987-02-01) Molecular crowding enhances facilitated diffusion of two human DNA glycosylases.Shannen L Cravens et al.Nucleic acids research, 43(8), 4087-4097 (2015-04-08) The screening and characterization of 6-aminopurine-based xanthine oxidase inhibitors.Jung-Feng Hsieh et al.Bioorganic & medicinal chemistry, 15(10), 3450-3456 (2007-03-24) Synthesis of 7-hydroxy(phenyl)ethylguanines by alkylation of 2-amino-6-chloropurine with allyl-protected bromohydrins.Jan Novák et al.Organic letters, 5(5), 637-639 (2003-02-28) Mode of action of 2-amino-6-chloro-1-deazapurine.L L Bennett et al.Biochemical pharmacology, 33(2), 261-271 (1984-01-15) Enzymatic synthesis of 2'-deoxyguanosine with nucleoside deoxyribosyltransferase-II.Kiyoshi Okuyama et al.Bioscience, biotechnology, and biochemistry, 67(5), 989-995 (2003-07-02) Testing nucleoside analogues as inhibitors of Bacillus anthracis spore germination in vitro and in macrophage cell culture.Zadkiel Alvarez et al.Antimicrobial agents and chemotherapy, 54(12), 5329-5336 (2010-10-06) Tautomeric purine forms of 2-amino-6-chloropurine (N9H10 and N7H10): structures, vibrational assignments, NBO analysis, hyperpolarizability, HOMO-LUMO study using B3 based density functional calculations.V Balachandran et al.Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 96, 340-351 (2012-06-19) Synthesis of enantiomeric N-(2-phosphonomethoxypropyl) derivatives of purine and pyrimidine bases. II. The synthon approach.Holy A, et al. Collection of Czechoslovak Chemical Communications, 60(8), 1309-1409 (1995) Lead compounds for antimalarial chemotherapy: purine base analogs discriminate between human and P. falciparum 6-oxopurine phosphoribosyltransferases.Dianne T Keough et al.Journal of medicinal chemistry, 49(25), 7479-7486 (2006-12-08) Asymmetric synthesis of novel apio carbocyclic nucleoside analogues as potential antiviral and antitumor agent.Lak Shin Jeong et al.Nucleosides, nucleotides & nucleic acids, 26(6-7), 721-724 (2007-12-11) Preparative electrochemical reduction of 2-amino-6-chloropurine and synthesis of 6-deoxyacyclovir, a fluorescent substrate of xanthine oxidase and a prodrug of acyclovir.J T Kusmierek et al.Acta chemica Scandinavica. Series B: Organic chemistry and biochemistry, 41(10), 701-707 (1987-11-01)
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