2425-25-4 ((Acetophos)

Acetophos(2425-25-4)名称与标识符

名称

英文别名:
Acetic acid,2-[(diethoxyphosphinyl)thio]-, ethyl ester;ethyl 2-diethoxyphosphorylsulfanylacetate;Acetic acid, ((diethoxyphosphinyl)thio)-, ethyl ester (9CI);Ethyl [(diethoxyphosphoryl)sulfanyl]acetate;SCHEMBL5933967;UNII-J4K0KB7I7Y;O,O-Diethyl S-(carbethoxy)methyl phosphorothiolate;Acetic acid, ((diethoxyphosphinyl)thio)-, ethyl ester;AI3-27526;PHOSPHOROTHIOIC ACID, O,O-DIETHYL S-CARBOETHOXYMETHYL ESTER;NS00127312;O,O-Diethyl S-carboethoxymethyl phosphorothioate;HSDB 2030;O,O-Diethyl S-carbethoxymethyl thiophosphate;ACETOXON;Ethyl ((diethoxyphosphinyl)thio)acetate;ACETOXON [HSDB];BRN 1793591;Acetaphos;Acetic acid, mercapto-, ethyl ester, S-ester with O,O-diethyl phosphorothioate;DTXSID8041581;Acetophos;Acetofos;Q27281190;O,O-Diethyl S-carboethoxymethyl thiophosphate;J4K0KB7I7Y;2425-25-4;Phosphorothioic acid, O,O-diethyl ester, S-ester with ethyl mercaptoacetate;

标识符

InChIKey:
ZRCQYAQOWIQUBA-UHFFFAOYSA-N
Inchi:
1S/C8H17O5PS/c1-4-11-8(9)7-15-14(10,12-5-2)13-6-3/h4-7H2,1-3H3
SMILES:
S(CC(=O)OCC)P(=O)(OCC)OCC

Acetophos(2425-25-4)物化性质

实验特性

  • PSA : 61.83

计算特性

  • 精确分子量 : 256.05351
  • 氢键供体数量 : 0
  • 氢键受体数量 : 6
  • 可旋转化学键数量 : 9
  • 同位素质量 : 256.05343181g/mol
  • 重原子数量 : 15
  • 复杂度 : 223
  • 同位素原子数量 : 0
  • 确定原子立构中心数量 : 0
  • 不确定原子立构中心数量 : 0
  • 确定化学键立构中心数量 : 0
  • 不确定化学键立构中心数量 : 0
  • 共价键单元数量 : 1
  • 疏水参数计算参考值(XlogP) : 0.9
  • 互变异构体数量 : 无
  • 表面电荷 : 0
  • 拓扑分子极性表面积 : 87.1Ų

Acetophos(2425-25-4)安全信息

Acetophos(2425-25-4)推荐厂家 更多厂家(2)

公司名称手机号/电话联系人QQ微信询单
西安德而塔生物科技有限公司 18133906270
18133906270
张女士 2590956145
询单
西安德而塔生物科技有限公司 18133906270
18133906270
张女士 2590956145
询单

Acetophos(2425-25-4)相关文献

  • 1. Reactions of lead tetra-acetate. Part XV. The oxidation of α- and cis- and trans-β-methylstyrene
    R. O. C. Norman,C. B. Thomas J. Chem. Soc. B 1968 994
  • 2. Propellane type derivatives of uric acid. X-Ray structure of 9-acetyl-4,5-(1-methoxyethylidenedioxy)-4,5-dihydrouric acid
    Mirko Poje,Boris Ro?i?,Ivan Vickovi?,Milenko Bruvo J. Chem. Soc. Chem. Commun. 1982 1338
  • 3. Reactions of γδ-unsaturated ketones with peracids. 2,7-Dioxabicyclo-[2,2,1]heptanes
    Y. Gaoni J. Chem. Soc. C 1968 2925
  • 4. Photo-bromination of carbohydrate derivatives. Part 3. C-5 bromination of penta-O-benzoyl-α- and -β-D-glucopyranose; a route to D-xylo-hexos-5-ulose derivatives and α-L-idopyranosides
    Robert J. Ferrier,Peter C. Tyler J. Chem. Soc. Perkin Trans. 1 1980 1528
  • 5. The photorearrangement of 6-acetoxy-3,5-bis(chloromethyl)-2,4,6-trimethylcyclohexa-2,4-dienone
    M. R. Morris,A. J. Waring J. Chem. Soc. C 1971 3266
  • 6. Reactions of acylated pentoses and acylated methyl pentosides with dibromomethyl methyl ether. Preparation of bromo-deoxy-pentoses
    Klaus Bock,Christian Pedersen,Poul Rasmussen J. Chem. Soc. Perkin Trans. 1 1973 1456