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4‐Phenyl‐1,2,4‐Triazoline‐3,5‐Dione 4‐Phenyl‐1,2,4‐Triazoline‐3.5‐土卫四
Pub Date : 2001-04-15 DOI: 10.1002/047084289X.RP139
J. M. Takacs
[4233-33-4] C8H5N3O2 (MW 175.16) InChI = 1S/C8H5N3O2/c12-7-9-10-8(13)11(7)6-4-2-1-3-5-6/h1-5H InChIKey = ISULLEUFOQSBGY-UHFFFAOYSA-N (highly reactive dienophile and enophile) Alternate Names: PTAD; N-phenyl-1,2,4-triazoline-3,5-dione. Physical Data: mp 179 °C (dec).2 Form Supplied in: PTAD and 4-methyl-1,2,4-triazoline-3,5-dione (MTAD) [13274-43-6]) are widely available commercially. Preparative Methods: there are several reported preparations,2-9 particularly for the in situ preparation. Handling, Storage, and Precautions: normal precautions against exposure to moisture and air; reacts with alcohols and water.
[4233-33-4] C8H5N3O2 (MW 175.16) InChI = 1S/C8H5N3O2/c12-7-9-10-8(13)11(7)6-4-2-1-3-5-6/h1-5H InChIKey = ISULLEUFOQSBGY-UHFFFAOYSA-N(高活性亲烯试剂和亲烯试剂)N-phenyl-1 2 4-triazoline-3 5-dione。物理数据:mp 179°C (dec)提供形式:PTAD和4-甲基-1,2,4-三唑啉-3,5-二酮(MTAD)[13274-43-6])在商业上广泛使用。制备方法:有几种报道的制备方法,2-9特别是原位制备。处理、储存和注意事项:防止暴露在潮湿和空气中的正常预防措施;与醇和水反应。
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引用次数: 0
Mercury(II) Oxide 汞氧化(II)
Pub Date : 2001-04-15 DOI: 10.1002/047084289X.RM038
E. Leahy
[21908-53-2] HgO (MW 216.59) InChI = 1S/Hg.O InChIKey = UKWHYYKOEPRTIC-UHFFFAOYSA-N (promotion of thio-Claisen rearrangement;2 deprotection of dithianes, dithiolanes,3 thioorthoesters;4 synthesis of tetrahydrofurans;5 oxidizing agent6-18) Alternate Name: mercuric oxide. Physical Data: mp 500 °C (dec); d 11.14 g cm−3. Solubility: sol dilute HCl, HNO3; insol water, ethanol. Form Supplied in: commercially available in both yellow and red crystalline forms. Handling, Storage, and Precautions: highly toxic; oxidizer; protect from light.
[21908-53-2] HgO (MW 216.59) InChI = 1S/Hg。O inchkey = UKWHYYKOEPRTIC-UHFFFAOYSA-N(促进硫- clisen重排;2二硫烷、二硫烷的脱保护;3硫代正酯;4四氢呋喃的合成;5氧化剂6-18)物理数据:mp 500°C (dec);D 11.14 g cm−3。溶解度:溶胶稀释HCl、HNO3;水,乙醇。供应形式:市售黄色和红色晶体形式。处理、储存和注意事项:剧毒;氧化剂;避光。
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引用次数: 0
Potassium Dodecanoate 钾Dodecanoate
Pub Date : 1900-01-01 DOI: 10.1002/047084289x.rn02385
Vikas Sikervar
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引用次数: 0
N ‐Acetylguanidine
Pub Date : 1900-01-01 DOI: 10.1002/047084289x.rn02383
Vikas Sikervar
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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
Pub Date : 1900-01-01 DOI: 10.1002/047084289x.rn02382
Vikas Sikervar
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引用次数: 0
Sodium 2‐Methyl‐2‐Propanethiolate 2检测甲基钠2 Propanethiolate应承担的
Pub Date : 1900-01-01 DOI: 10.1002/047084289x.rn02387
Vikas Sikervar
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引用次数: 0
1‐Hydroxy‐1,2‐Benziodoxol‐3(1 H )‐One 1 1.2‐1‐Hydroxy‐Benziodoxol‐3 (H)‐1万
Pub Date : 1900-01-01 DOI: 10.1002/047084289x.rn00605.pub2
V. Zhdankin
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引用次数: 0
Tetramethylchloroformamidinium Hexafluorophosphate Tetramethylchloroformamidinium方法
Pub Date : 1900-01-01 DOI: 10.1002/047084289x.rn02314
H. Lebel
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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‐
Pub Date : 1900-01-01 DOI: 10.1002/047084289x.rn02367
Junichiro Kanazawa, M. Uchiyama
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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
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
期刊
Encyclopedia of Reagents for Organic Synthesis
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