CAS: 1212-08-4; Benzenethiosulfonicacids-Phenylester

相似化合物

3541-14-8 2943-42-2 1142-97-8

上下游产品

CAS号108-98-5 硫酚 | CAS号882-33-7 二苯二硫醚 | CAS号98-09-9 苯磺酰氯 | CAS号1073-67-2 对氯苯乙烯 | CAS号292638-84-7 phenylene-ethylene | CAS号622-97-9 4-甲基苯乙烯 | CAS号4972-29-6 苯亚磺酰氯 | CAS号121434-38-6 phenyliodonium ... | CAS号1208-20-4 Benzenesulfinot... | CAS号1712-70-5 4-氯-α-甲基苯乙烯 | CAS号456-56-4 苯基三氟甲基硫醚 | CAS号141075-87-8 1-fluoroethenyl... | CAS号368-43-4 苯磺酰氟 | CAS号139-66-2 苯硫醚 | CAS号92-52-4 联苯 | CAS号618-41-7 苯亚磺酸 | CAS号882-33-7 二苯二硫醚 | CAS号108-98-5 硫酚

Diphenyl Tetrasulfide置于四氯化碳,乙醚,氯体系中,化学反应生成S-苯基硫代苯基砜
参考文献:Lecher,Chemische Berichte,1925,Vol. 58,P. 415
标题:Lecher,Chemische Berichte,1925,Vol. 58,P. 415

专利信息

专利号:US-2006009479-A1
优先权日:2004-07-09
标 题 :Process for the synthesis of hydromorphone
发明人：BAILEY TIMOTHY S; GEE PAUL S; REZAIE ROBERT
权利人:BAILEY TIMOTHY S; GEE PAUL S; REZAIE ROBERT
摘要:There is described a method for converting oripavine to hydromorphone or a physiologically acceptable salt thereof such as hydromorphone hydrochloride involving generation of 8,14-dihydrooripavine utilising diimine.

专利号:US-5081138-A
优先权日:1986-12-17
标题:3-hetero-substituted-n-benzyl-indoles and prevention of leucotriene synthesis therewith
发明人：GILLARD JOHN W; MORTON HOWARD E; FORTIN REJEAN; GUINDON YVAN
权利人:MERCK FROSST CANADA INC
摘要:Compounds having the formula: are inhibitors of leukotriene biosynthesis. These compounds are useful as anti-asthmatic, anti-allergic, anti-inflammatory, and cytoprotective agents. They are also useful in treating diarrhea, hypertension, angina, platelet aggregation, cerebral spasm, premature labor, spontaneous abortion, dysmenorrhea, and migraine.

专利号:US-2005240034-A1
优先权日:2002-05-07
标 题 :Artemisinin-based peroxide compounds as broad spectrum anti-infective agents
发明人：AVERY MITCHELL; MURALEEDHARAN KANNOTH M
权利人:AVERY MITCHELL; MURALEEDHARAN KANNOTH M
摘要:Described herein is the synthesis, bioassay results and utility of new C- 9 and C- 10 substituted artemisinin derivatives with easily functionalizable groups attached to the artemisinin skeleton through carbon chain or heteroatoms. Described also is the demonstration of this class of compounds for their broad-spectrum anti-parasitic activity. Certain of these analogs possess noticeable cytotoxicity deliberately focused on treatment of cancerous diseases.