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4‐Phenyl‐1,2,4‐Triazoline‐3,5‐Dione 4‐Phenyl‐1,2,4‐Triazoline‐3.5‐土卫四
Encyclopedia of Reagents for Organic Synthesis Pub Date : 2001-04-15 DOI: 10.1002/047084289X.RP139
J. M. Takacs
{"title":"4‐Phenyl‐1,2,4‐Triazoline‐3,5‐Dione","authors":"J. M. Takacs","doi":"10.1002/047084289X.RP139","DOIUrl":"https://doi.org/10.1002/047084289X.RP139","url":null,"abstract":"[4233-33-4] C8H5N3O2 (MW 175.16) \u0000 \u0000 \u0000 \u0000 \u0000 \u0000InChI = 1S/C8H5N3O2/c12-7-9-10-8(13)11(7)6-4-2-1-3-5-6/h1-5H \u0000 \u0000 \u0000 \u0000InChIKey = ISULLEUFOQSBGY-UHFFFAOYSA-N \u0000 \u0000 \u0000 \u0000(highly reactive dienophile and enophile) \u0000 \u0000 \u0000 \u0000Alternate Names: PTAD; N-phenyl-1,2,4-triazoline-3,5-dione. \u0000 \u0000 \u0000 \u0000Physical Data: mp 179 °C (dec).2 \u0000 \u0000 \u0000 \u0000Form Supplied in: PTAD and 4-methyl-1,2,4-triazoline-3,5-dione (MTAD) [13274-43-6]) are widely available commercially. \u0000 \u0000 \u0000 \u0000Preparative Methods: there are several reported preparations,2-9 particularly for the in situ preparation. \u0000 \u0000 \u0000 \u0000Handling, Storage, and Precautions: normal precautions against exposure to moisture and air; reacts with alcohols and water.","PeriodicalId":11669,"journal":{"name":"Encyclopedia of Reagents for Organic Synthesis","volume":"20 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2001-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87316181","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mercury(II) Oxide 汞氧化(II)
Encyclopedia of Reagents for Organic Synthesis Pub Date : 2001-04-15 DOI: 10.1002/047084289X.RM038
E. Leahy
{"title":"Mercury(II) Oxide","authors":"E. Leahy","doi":"10.1002/047084289X.RM038","DOIUrl":"https://doi.org/10.1002/047084289X.RM038","url":null,"abstract":"[21908-53-2] HgO (MW 216.59) \u0000 \u0000 \u0000 \u0000 \u0000 \u0000InChI = 1S/Hg.O \u0000 \u0000 \u0000 \u0000InChIKey = UKWHYYKOEPRTIC-UHFFFAOYSA-N \u0000 \u0000 \u0000 \u0000(promotion of thio-Claisen rearrangement;2 deprotection of dithianes, dithiolanes,3 thioorthoesters;4 synthesis of tetrahydrofurans;5 oxidizing agent6-18) \u0000 \u0000 \u0000 \u0000Alternate Name: mercuric oxide. \u0000 \u0000 \u0000 \u0000Physical Data: mp 500 °C (dec); d 11.14 g cm−3. \u0000 \u0000 \u0000 \u0000Solubility: sol dilute HCl, HNO3; insol water, ethanol. \u0000 \u0000 \u0000 \u0000Form Supplied in: commercially available in both yellow and red crystalline forms. \u0000 \u0000 \u0000 \u0000Handling, Storage, and Precautions: highly toxic; oxidizer; protect from light.","PeriodicalId":11669,"journal":{"name":"Encyclopedia of Reagents for Organic Synthesis","volume":"s3-10 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2001-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90806465","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Potassium Dodecanoate 钾Dodecanoate
Encyclopedia of Reagents for Organic Synthesis Pub Date : 1900-01-01 DOI: 10.1002/047084289x.rn02385
Vikas Sikervar
{"title":"Potassium Dodecanoate","authors":"Vikas Sikervar","doi":"10.1002/047084289x.rn02385","DOIUrl":"https://doi.org/10.1002/047084289x.rn02385","url":null,"abstract":"","PeriodicalId":11669,"journal":{"name":"Encyclopedia of Reagents for Organic Synthesis","volume":"92 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74543076","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
N ‐Acetylguanidine
Encyclopedia of Reagents for Organic Synthesis Pub Date : 1900-01-01 DOI: 10.1002/047084289x.rn02383
Vikas Sikervar
{"title":"N\u0000 ‐Acetylguanidine","authors":"Vikas Sikervar","doi":"10.1002/047084289x.rn02383","DOIUrl":"https://doi.org/10.1002/047084289x.rn02383","url":null,"abstract":"","PeriodicalId":11669,"journal":{"name":"Encyclopedia of Reagents for Organic Synthesis","volume":"15 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74768012","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
1,3‐Di‐Boc‐2‐(trifluoromethanesulfonyl)guanidine 1,3必经Di必经中行还是2 (trifluoromethanesulfonyl)胍
Encyclopedia of Reagents for Organic Synthesis Pub Date : 1900-01-01 DOI: 10.1002/047084289x.rn02382
Vikas Sikervar
{"title":"1,3‐Di‐Boc‐2‐(trifluoromethanesulfonyl)guanidine","authors":"Vikas Sikervar","doi":"10.1002/047084289x.rn02382","DOIUrl":"https://doi.org/10.1002/047084289x.rn02382","url":null,"abstract":"","PeriodicalId":11669,"journal":{"name":"Encyclopedia of Reagents for Organic Synthesis","volume":"36 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89779044","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Sodium 2‐Methyl‐2‐Propanethiolate 2检测甲基钠2 Propanethiolate应承担的
Encyclopedia of Reagents for Organic Synthesis Pub Date : 1900-01-01 DOI: 10.1002/047084289x.rn02387
Vikas Sikervar
{"title":"Sodium 2‐Methyl‐2‐Propanethiolate","authors":"Vikas Sikervar","doi":"10.1002/047084289x.rn02387","DOIUrl":"https://doi.org/10.1002/047084289x.rn02387","url":null,"abstract":"","PeriodicalId":11669,"journal":{"name":"Encyclopedia of Reagents for Organic Synthesis","volume":"33 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86927624","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
1‐Hydroxy‐1,2‐Benziodoxol‐3(1 H )‐One 1 1.2‐1‐Hydroxy‐Benziodoxol‐3 (H)‐1万
Encyclopedia of Reagents for Organic Synthesis Pub Date : 1900-01-01 DOI: 10.1002/047084289x.rn00605.pub2
V. Zhdankin
{"title":"1‐Hydroxy‐1,2‐Benziodoxol‐3(1\u0000 \u0000 H\u0000 \u0000 )‐One\u0000 1","authors":"V. Zhdankin","doi":"10.1002/047084289x.rn00605.pub2","DOIUrl":"https://doi.org/10.1002/047084289x.rn00605.pub2","url":null,"abstract":"","PeriodicalId":11669,"journal":{"name":"Encyclopedia of Reagents for Organic Synthesis","volume":"723 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78743425","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Tetramethylchloroformamidinium Hexafluorophosphate Tetramethylchloroformamidinium方法
Encyclopedia of Reagents for Organic Synthesis Pub Date : 1900-01-01 DOI: 10.1002/047084289x.rn02314
H. Lebel
{"title":"Tetramethylchloroformamidinium Hexafluorophosphate","authors":"H. Lebel","doi":"10.1002/047084289x.rn02314","DOIUrl":"https://doi.org/10.1002/047084289x.rn02314","url":null,"abstract":"","PeriodicalId":11669,"journal":{"name":"Encyclopedia of Reagents for Organic Synthesis","volume":"24 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75177797","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
1,3,2‐Dioxaborolane, 2‐[3‐(Dimethylphenylsilyl)bicyclo[1.1.1]pent‐1‐yl]‐4,4,5,5‐tetramethyl‐ 1,3,2‐Dioxaborolane 2‐[3]‐Dimethylphenylsilyl bicyclo [1.1.1] (pent‐1‐yl]‐4,4,5,5‐tetramethyl‐
Encyclopedia of Reagents for Organic Synthesis Pub Date : 1900-01-01 DOI: 10.1002/047084289x.rn02367
Junichiro Kanazawa, M. Uchiyama
{"title":"1,3,2‐Dioxaborolane, 2‐[3‐(Dimethylphenylsilyl)bicyclo[1.1.1]pent‐1‐yl]‐4,4,5,5‐tetramethyl‐","authors":"Junichiro Kanazawa, M. Uchiyama","doi":"10.1002/047084289x.rn02367","DOIUrl":"https://doi.org/10.1002/047084289x.rn02367","url":null,"abstract":"","PeriodicalId":11669,"journal":{"name":"Encyclopedia of Reagents for Organic Synthesis","volume":"58 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72581537","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
tert ‐Butyl ( Z )‐((1 H ‐pyrazol‐1‐yl)((2,2,2‐Trifluoroacetyl)imino)methyl)carbamate 叔丁基(Z)‐((1 H‐吡唑‐1‐基)((2,2,2‐三氟乙酰基)亚氨基)甲基)氨基甲酸酯
Encyclopedia of Reagents for Organic Synthesis Pub Date : 1900-01-01 DOI: 10.1002/047084289x.rn02315
H. Lebel
{"title":"tert\u0000 \u0000 ‐Butyl (\u0000 \u0000 Z\u0000 \u0000 )‐((1\u0000 \u0000 H\u0000 \u0000 ‐pyrazol‐1‐yl)((2,2,2‐Trifluoroacetyl)imino)methyl)carbamate","authors":"H. Lebel","doi":"10.1002/047084289x.rn02315","DOIUrl":"https://doi.org/10.1002/047084289x.rn02315","url":null,"abstract":"","PeriodicalId":11669,"journal":{"name":"Encyclopedia of Reagents for Organic Synthesis","volume":"13 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73914745","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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