4-Methylbenzenesulfonhydrazide 对甲苯磺酰肼
CAS 1576-35-8 MFCD00007588
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分类
- {SNA} Building Blocks, Chemical Synthesis, Organic Building Blocks, Sulfonyl Hydrazides, Sulfur Compounds
相关文献及参考
- Beil. 11 ,IV,470
- Several simple methods are known for cleavage of tosylhydrazones, including:
- For a reviews of the Bamford-Stevens, Shapiro-Heath and related reactions, see: Org. React., 23, 405 (1976); 39, 1 (1990). For an example (bornene: 63-66% yield from camphor tosylhydrazone and MeLi), see: Org. Synth. Coll., 6, 172 (1988).
- React
- Reaction of tosylhydrazones with base leads to alkenes (Bamford-Stevens reaction): J. Chem. Soc., 4735 (1952). Dianion formation from the tosylhydrazone with an alkyllithium or LDA results in a vinyllithium intermediate, which, on protonation, also gives the alkene (Shapiro-Heath reaction). With unsymmetrical tosylhydrazones, this is a useful synthe
- Exchange with refluxing acetone: J. Org. Chem., 40, 3302 (1975); acetone/ BF3 etherate: Synthesis, 456 (1976); Amberlyst. 15 in aqueous acetone: J. Chem. Soc., Perkin 1, 2563 (1988).
- Reduction of tosylhydrazones to alkanes by NaBH4 is a mild alternative to the Clemmensen and Wolff-Kishner methods: Chem. Ind. (London), 153, 1689 (1964). NaBH4 in AcOH is a more selective system: J. Org. Chem., 43, 2299 (1978). For reduction of a steroidal ketone by catecholborane, see: Org. Synth. Coll., 6, 293 (1988). Aliphatic tosylhydrazones are also reduced to methylenes by NaBH3CN, effective even for hindered ketones. For a study of the mechanism of this reduction, see: J. Org. Chem., 54, 4175 (1989).
- Precursor of the versatile synthetic intermediates, tosylhydrazones. For a brief feature on tosylhydrazones, see: Synlett, 1844 (1999). Preparation using AcOH rather than mineral acid was found to reduce azine formation: Synthesis, 957 (1984).
- Reaction of tosylhydrazones with base leads to alkenes (Bamford-Stevens reaction): J. Chem. Soc., 4735 (1952). Dianion formation from the tosylhydrazone with an alkyllithium or LDA results in a vinyllithium intermediate, which, on protonation, also gives the alkene (Shapiro-Heath reaction). With
安全信息
GHS Symbol


- H242 Heating may cause a fire 加热可能会引起火灾
- H301 Toxic if swallowed 吞食有毒
- H302 Harmful if swallowed 吞食有害
- H319 Causes serious eye irritation 严重刺激眼睛
- P201 Obtain special instructions before use. 使用前获取专门指示。
- P202 Do not handle until all safety precautions have been read and understood. 已阅读并理解所有的安全预防措施之前,切勿操作。
- P210 Keep away from heat/sparks/open flames/hot surfaces. — No smoking. 远离热源/火花/明火/热的表面。——禁止吸烟。
- P220 Keep/Store away from clothing/…/combustible materials. 保持远离/贮存远离服装/....../可燃材料。
- P234 Keep only in original container. 只保留在原来的容器中。
- P261 Avoid breathing dust/fume/gas/mist/vapours/spray. 避免吸入粉尘/烟/气体/烟雾/蒸汽/喷雾。
- P264 Wash hands thoroughly after handling. 处理后要彻底洗净双手。
- P270 Do not eat, drink or smoke when using this product. 使用本产品时不要吃东西,喝水或吸烟。
- 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。
- P301+P310
- P301+P310+P330
- P301+P312
- P302+P350
- P302+P352+P332+P313+P362+P364
- P305+P351+P338
- P305+P351+P338+P337+P313
- P308+P313
- P321 Specific treatment (see … on this label). 具体治疗(见本标签上的)。
- P330 Rinse mouth. 漱口
- P332+P313
- P337+P313
- 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
- P370+P378
- P403+P235
- P405 Store locked up. 上锁保管。
- P411 Store at temperatures not exceeding … oC/…oF. 储存在温度不超过…oC /…oF。
- P420 Store away from other materials. 远离其他材料。
- P501 Dispose of contents/container to..… 处理内容物/容器.....
- R11 Highly flammable 非常易燃
- R44 Risk of explosion if heated under confinement 密封下加热有爆炸危险
- R22 Harmful if swallowed 吞咽有害
TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : Intraperitoneal SPECIES OBSERVED : Rodent - mouse DOSE/DURATION : 1200 mg/kg TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value REFERENCE : RPTOAN Russian Pharmacology and Toxicology (English Translation). Translation of FATOAO. (Euromed Pub., 33, Woodlands Rd., Surbiton, Surrey, UK) V.30- 1967- Volume(issue)/page/year: 36,27,1973
其他信息
- MSDS 信息:p-Toluenesulfonhydrazide(1576-35-8).msds
- Acros Organics:对甲苯磺酰肼 4-Methylbenzenesulfonhydrazide, 97%(1576-35-8)
- 检测方法:HPLC,NMR,MS
- Sigma Aldrich:1576-35-8(sigmaaldrich)
- 方法一:对甲苯磺酰氯与水合肼在苯介质中于60-70℃进行缩合,排放的氯化氢用水吸收。过滤,水洗,于65℃干燥得发泡剂TSH。滤液中的苯层供循环使用,水层可回收硫酸肼。原料消耗(kg/t)对甲苯磺酰氯(96.8%) 1110水合肼(40%) 820苯 520
- 用途一:用作天然胶、合成胶及多种塑料的发泡剂及用于有机合成中
- 图谱信息:对甲苯磺酰肼(1576-35-8)核磁图( 13 CNMR) 对甲苯磺酰肼(1576-35-8)质谱(MS) 对甲苯磺酰肼(1576-35-8)核磁图( 1 HNMR) 对甲苯磺酰肼(1576-35-8)红外图谱(IR2) 对甲苯磺酰肼(1576-35-8)红外图谱(IR1)
- 存储注意事项:氮气保护
- TCI Shanghai:4-甲苯磺酰肼 p-Toluenesulfonyl Hydrazide,>;98.0%(LC)(1576-35-8)
- 对甲苯磺酰肼价格(试剂级):更新日期 产品编号 产品名称 包装 价格 2014/06/02 T0286 对甲苯磺酰肼 p-Toluenesulfonyl Hydrazide 25G 130元 2014/06/02 T0286 对甲苯磺酰肼 p-Toluenesulfonyl Hydrazide 500G 720元 2010/06/21 157861000 对甲苯磺酰肼 4-Methylbenzenesulfonhydrazide 97% 100 GR 447元
- 上游原料:4-甲苯磺酰氯 --> 硫酸肼
- 海关编码:29280090
- 用途二:用作天然橡胶、合成橡胶及多种塑料的发泡剂,使塑料及橡胶制品产生细微闭孔结构,制品的收缩率小,抗撕裂强度大。
- 敏感性:Moisture Sensitive
- MOL 文件:1576-35-8.mol
- Alfa Aesar:对甲苯磺酰肼,98% p-Toluenesulfonyl hydrazide, 98%(1576-35-8)