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脲过氧化氢加合物_分子结构_CAS_124-43-6)
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脲过氧化氢加合物

产品号 L13940 公司名称 Alfa Aesar
CAS号 124-43-6 公司网站 http://www.alfa.com
分子式 CH6N2O3 电 话
分子量 94.06994 传 真
纯 度 97% 电子邮件
保 存 Chembase数据库ID: 126396

产品价格信息

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产品别名

标题
Urea hydrogen peroxide adduct
IUPAC标准名
peroxol; urea
IUPAC传统名
hydrogen peroxide; urea
别名
Percarbamide
Hydrogen peroxide urea adduct

产品登记号

MDL号 MFCD00013119
EC号 204-701-4
默克索引号 141782
Beilstein号 3680414
CAS号 124-43-6

产品性质

纯度 97%
熔点 ca 90°C dec.
GHS危险品标识 GHS03
GHS危险品标识 GHS05
GHS危险声明 H272-H314-H318
欧盟危险性物质标志 腐蚀性(Corrosive) 腐蚀性(Corrosive) (C)
欧盟危险性物质标志 氧化性(Oxidising) 氧化性(Oxidising) (O)
GHS警示性声明 P221-P210-P303+P361+P353-P305+P351+P338-P405-P501A
危险公开号 8-34
RTECS编号 T4860000
安全公开号 17-20-26-36/37/39-45-60
保存注意事项 Hygroscopic
TSCA收录
联合国危险货物等级 5.1
联合国危险货物编号 UN1511
联合国危险货物包装类别(PG) III

产品详细信息

参考文献

  • For use in partial oxidation of nitriles to amides, see: Synth. Commun., 23, 3149 (1993).
  • In combination with phthalic anhydride is an effective mild and safe oxidant for N-heteroaromatic compounds and tertiary amines to N-oxides: Chem. Ber., 125, 1965 (1992)
  • Useful, low-hazard alternative to high-concentration H2O2 in epoxidations, Baeyer-Villiger reactions, N-oxidations, etc.: Synlett, 533 (1990). Alkenes can be epoxidized in high yield in 1,1,1,3,3,3-Hexafluoro-2-propanol, A12747 as solvent: Eur. J. Org. Chem., 3290 (2002). For use in combination with N,N'-Dicyclohexylcarbodiimide, A10973, in epoxidation of alkenes, see: J. Org. Chem., 63, 1730 (1998); in combination with Maleic anhydride, A12178, for epoxidation and Baeyer-Villiger reactions: Heterocycles, 36, 1075 (1993). For an extensive review of the Baeyer-Villiger reaction, see: Org. React., 43, 251 (1993).
  • Can be used to generate the powerful oxidant peroxytrifluoroacetic acid from TFAA, avoiding the use of hazardous 90% H2O2: Tetrahedron Lett., 33, 4835 (1992). The same system has also been reported for oxidation of electron-deficient pyridines to the N-oxides: Tetrahedron Lett., 41, 2299 (2000). Similarly, performic acid can be generated in situ, providing a mild system for oxidation of aromatic aldehydes to benzoic acids: Synth. Commun., 31, 2195 (2001). See also Sodium percarbonate, A16045.