Trimethylsulfonium Iodide 碘化三甲基锍
CAS 2181-42-2 MFCD00011632
信息真实价格透明
资金保障
专业采购外包团队在线服务
信息真实价格透明
资金保障
专业采购外包团队在线服务
品牌质保精细包装
现货库存
一流品牌服务
分类
- {SA} Building Blocks, C-C Bond Formation, Chemical Synthesis, Organic Building Blocks, Others, Sulfonium/Sulfoxonium Compounds, Sulfur Compounds, Synthetic Reagents
- {SNA} Building Blocks, C-C Bond Formation, Chemical Synthesis, Organic Building Blocks, Others, Sulfonium/Sulfoxonium Compounds, Sulfur Compounds, Synthetic Reagents
- {SNA} Building Blocks, C-C Bond Formation, Chemical Synthesis, Organic Building Blocks, Other Synthetic Reagents for C-C Bond Formation, Sulfonium/Sulfoxonium Compounds, Sulfur Compounds, Synthetic Reagents
产品应用
- 亚甲基转移试剂,碳复合物转换成环氧化物或烯丙基醇。
相关文献及参考
- Other conditions for addition to aldehydes include: phase-transfer catalysis: Angew. Chem. Int. Ed., 12, 845 (1973), KOH in acetonitrile: Tetrahedron Lett., 23, 5283 (1982), or KF on alumina: Tetrahedron, 41, 1259 (1985). With aryl aldehydes, the use of KO-t-Bu gives improved results by suppressing the competing Cannizzaro reaction: Org. Prep. Proced. Int., 27, 219 (1995). A simplified, solvent-free method employing KO-t-Bu has been reported for ketones: Heterocycles, 46, 185 (1997). With excess of the sulfonium ylide, ketones or epoxides give good yields of allylic alcohols, whereas aldehydes give poor yields. Under similar conditions, the sulfoxonium ylide gives oxetanes: Tetrahedron Lett., 35, 2009, 5449 (1994).
- Beilstein: 1,IV,1280
- Methylene transfer to allylic, propargylic, benzylic and primary alkyl halides and sulfonates results in formation of termi
- The ylide, generated with strong base, is a powerful methylene transfer reagent, converting aldehydes and ketones to epoxides; reaction with ɑß-enones also gives epoxides (contrast Trimethylsulfoxonium iodide, A14589): J. Am. Chem. Soc., 87, 1353 (1965):
- Methylene transfer to imines and arylhydrazones gives aziridines and N-arylaminoaziridines respectively: Synthesis, 330 (1983).
- Addition to vinyl sulfones gives cyclopropyl sulfones: J. Org. Chem., 29, 3277 (1964). Similarly, vinylsulfonates and sulfonamides give cyclopropanes in fair to good yields: J. Org. Chem., 33, 3849 (1968).
安全信息
- P280 Wear protective gloves/protective clothing/eye protection/face protection. 戴防护手套/防护服/眼睛的保护物/面部保护物。
- P362 Take off contaminated clothing and wash before reuse. 脱掉污染的衣服,清洗后方可重新使用
- P264 Wash hands thoroughly after handling. 处理后要彻底洗净双手。
- P261 Avoid breathing dust/fume/gas/mist/vapours/spray. 避免吸入粉尘/烟/气体/烟雾/蒸汽/喷雾。
- P305+P351+P338
- P302+P352+P332+P313+P362+P364
- P305+P351+P338+P337+P313
GHS Symbol
- H315 Causes skin irritation 会刺激皮肤
- H319 Causes serious eye irritation 严重刺激眼睛
- H335 May cause respiratory irritation 可能导致呼吸道刺激
- S36 Wear suitable protective clothing 穿戴适当的防护服;
- S26 In case of contact with eyes, rinse immediately with plenty of water and seek medical advice 眼睛接触后,立即用大量水冲洗并征求医生意见;
- S37 Wear suitable gloves 戴适当手套;
- R36/37/38 Irritating to eyes, respiratory system and skin 对眼睛、呼吸系统和皮肤有刺激性
TYPE OF TEST : LDLo - Lowest published lethal dose ROUTE OF EXPOSURE : Subcutaneous SPECIES OBSERVED : Rodent - mouse DOSE/DURATION : 300 mg/kg TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value REFERENCE : JPETAB Journal of Pharmacology and Experimental Therapeutics. (Williams & Wilkins Co., 428 E. Preston St., Baltimore, MD 21202) V.1- 1909/10- Volume(issue)/page/year: 25,315,1925
TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : Intravenous SPECIES OBSERVED : Rodent - mouse DOSE/DURATION : 18 mg/kg TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value REFERENCE : CSLNX* U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. (Aberdeen Proving Ground, MD 21010) Volume(issue)/page/year: NX#02185
TYPE OF TEST : LDLo - Lowest published lethal dose ROUTE OF EXPOSURE : Intraperitoneal SPECIES OBSERVED : Rodent - rat DOSE/DURATION : 88 mg/kg TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value REFERENCE : TXAPA9 Toxicology and Applied Pharmacology. (Academic Press, Inc., 1 E. First St., Duluth, MN 55802) V.1- 1959- Volume(issue)/page/year: 20,135,1971
其他信息
- TCI Shanghai:碘化三甲基锍 Trimethylsulfonium Iodide,>;98.0%(T)(2181-42-2)
- 溶于水。
- Acros Organics:三甲基碘化硫嗡 Trimethylsulfonium iodide, 98%(2181-42-2)
- F:8
- 海关编码:29309070
- 用途一:亚甲基转移试剂,碳复合物转换成环氧化物或烯丙基醇。
- Alfa Aesar:三甲基碘化锍,99% Trimethylsulfonium iodide, 99%(2181-42-2)
- Sigma Aldrich:2181-42-2(sigmaaldrich)
- MSDS 信息:Trimethylsulfonium iodide(2181-42-2).msds
- 敏感性:Light Sensitive
- MOL 文件:2181-42-2.mol
- 图谱信息:三甲基碘化锍(2181-42-2)质谱(MS) 三甲基碘化锍(2181-42-2)核磁图( 13 CNMR) 三甲基碘化锍(2181-42-2)红外图谱(IR1) 三甲基碘化锍(2181-42-2)核磁图( 1 HNMR) 三甲基碘化锍(2181-42-2)红外图谱(IR2)
- 三甲基碘化锍价格(试剂级):更新日期 产品编号 产品名称 包装 价格 2014/06/02 T1056 三甲基碘化锍 Trimethylsulfonium Iodide 25G 404元 2014/06/02 T1056 三甲基碘化锍 Trimethylsulfonium Iodide 500G 3140元 2010/06/21 140255000 三甲基碘化锍 Trimethylsulfonium iodide 98% 500 GR 3962元