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羟基甲苯磺酰碘苯_分子结构_CAS_27126-76-7)
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羟基甲苯磺酰碘苯

产品号 56517 公司名称 Sigma Aldrich
CAS号 27126-76-7 公司网站 http://www.sigmaaldrich.com
分子式 C13H13IO4S 电 话 1-800-521-8956
分子量 392.20939 传 真
纯 度 ≥97.0% (AT) 电子邮件
保 存 Chembase数据库ID: 32051

产品价格信息

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产品别名

标题
[Hydroxy(tosyloxy)iodo]benzene
IUPAC标准名
hydroxy phenyl 4-methylbenzene-1-sulfonoperoxoyl iodide
IUPAC传统名
hydroxy phenyl 4-methylbenzenesulfonoperoxoyl iodide
别名
Koser’s reagent
Koser 试剂
Hydroxy(phenyl)iodo tosylate
[Hydroxy(4-toluenesulfonato)iodo]benzene
Iodosobenzene-I-mono-p-toluenesulfonate
HTIB
NSC 294176
Phenyliodosyl hydroxide tosylate
Hydroxy(4-methylbenzenesulfonato-O)phenyliodine
羟基(甲苯磺酰氧代)碘苯

产品登记号

CAS号 27126-76-7
MDL号 MFCD00011547
Beilstein号 2150074

产品性质

德国WGK号 3
GHS危险品标识 GHS07
GHS警示词 Warning
GHS危险声明 H315-H319
欧盟危险性物质标志 刺激性(Irritant) 刺激性(Irritant) (Xi)
MSDS下载 下载链接
个人保护装置 dust mask type N95 (US), Eyeshields, Gloves
GHS警示性声明 P305 + P351 + P338
危险公开号 36/38
安全公开号 26-36
级别 purum
线性分子式 CH3C6H4SO3I(OH)C6H5
纯度 ≥97.0% (AT)
熔点 131-137 °C(lit.)
熔点 131-137 °C

产品详细信息

详细说明 (English)
Other Notes
Reagent for the selective syn-1,2-ditosyloxylation of alkenes, tosyloxylation reactions and other transformations 9,10,11
Application
Reactant for:
• Ligand-free palladium-catalyzed Heck-type coupling reactions1
• Preparation of carbodiimides via dehydrosulfurization of thioureas2
• Preparation of nitriles by oxidative conversion of alcohols, aldehydes, and amines3
• Preparation of substituted anilines via aromatic aldoxime reaction4
• Preparation of tetrahydrofurans by oxidative cyclization of homoallylic alcohols5
• Preparation of isoxazoline N-Oxides from β-hydroxyketoximes via oxidative N-O coupling6
• Ring expansion in synthesis of aminopeptidase inhibitors7
• Oxidation and protonation reactions in acidic conditions8
详细说明 (简体中文)
Other Notes
用于烯烃的选择性顺式-1,2-二对甲苯磺酰氧基化反应、对甲苯磺酰氧基化反应和其他转化的试剂9,10,11
Application
Reactant for:
• Ligand-free palladium-catalyzed Heck-type coupling reactions1
• Preparation of carbodiimides via dehydrosulfurization of thioureas2
• Preparation of nitriles by oxidative conversion of alcohols, aldehydes, and amines3
• Preparation of substituted anilines via aromatic aldoxime reaction4
• Preparation of tetrahydrofurans by oxidative cyclization of homoallylic alcohols5
• Preparation of isoxazoline N-Oxides from β-hydroxyketoximes via oxidative N-O coupling6
• Ring expansion in synthesis of aminopeptidase inhibitors7
• Oxidation and protonation reactions in acidic conditions8

参考文献