102-10-3 (亚磷酸二苯酯,Phosphorous acid, diphenyl ester)

快速询单

结构式：

亚磷酸二苯酯MOL文件

CAS号：

102-10-3

中文名称：

亚磷酸二苯酯

英文名称：

Phosphorous acid, diphenyl ester

分子式：

C₁₂H₁₀O₃P

分子量：

233.179764270782

API：

Acotiamide

亚磷酸二苯酯(102-10-3)名称与标识符

名称

英文别名：

Phosphorous acid, diphenyl ester;diphenyl phosphite;102-10-3;DTXSID70633743;Diphenoxyphosphanolate;C12H10O3P-;Bisphenyl phosphite;AKOS024437898;KUMNEOGIHFCNQW-UHFFFAOYSA-N;

标识符

InChIKey：

KUMNEOGIHFCNQW-UHFFFAOYSA-N

Inchi：

1S/C12H10O3P/c13-16(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h1-10H/q-1

SMILES：

P([O-])(OC1C=CC=CC=1)OC1C=CC=CC=1

亚磷酸二苯酯(102-10-3)物化性质

实验特性

PSA : 41.52

计算特性

精确分子量 : 234.04463
氢键供体数量 : 0
氢键受体数量 : 3
可旋转化学键数量 : 4
同位素质量 : 233.03675617g/mol
重原子数量 : 16
复杂度 : 169
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） : 3.1
拓扑分子极性表面积 : 41.5Å²

亚磷酸二苯酯(102-10-3)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
深圳菲斯生物科技有限公司	18925202235	周美娇	2850179284		询单
湖北瑞诺医药科技有限公司	13165688766	汪经理	3008058303		询单

亚磷酸二苯酯(102-10-3)相关文献

1. 796. Interaction of boron chlorides with dialkyl or diaryl hydrogen phosphites
R. Bedell,M. J. Frazer,W. Gerrard J. Chem. Soc. 1960 4037
2. BF3–Et2O promoted bifunctionalization of aldehydes for the synthesis of arylmethyl substituted organophosphorus compounds
Sajjad Ahmed,Zoya Shafeeq,Feroze Hussain,Qazi Naveed Ahmed Chem. Commun. 2023 59 12334
3. First example of quinine-squaramide catalyzed enantioselective addition of diphenyl phosphite to ketimines derived from isatins
Jimil George,B. Sridhar,B. V. Subba Reddy Org. Biomol. Chem. 2014 12 1595
4. Thiourea catalyzed organocatalytic enantioselective Michael addition of diphenyl phosphite to nitroalkenes
Ana Alcaine,Eugenia Marqués-López,Pedro Merino,Tomás Tejero,Raquel P. Herrera Org. Biomol. Chem. 2011 9 2777
5. A novel ketone olefination via organozinc reagents in the presence of diphenyl phosphite
Hua Cui,Ying Li,Songlin Zhang Org. Biomol. Chem. 2012 10 2862
6. A new, efficient and recyclable [Ce(l-Pro)]2(Oxa) heterogeneous catalyst used in the Kabachnik–Fields reaction
Caren D. G. da Silva,Aline R. Oliveira,Mariana P. D. Rocha,Ramesh Katla,Eriton Rodrigo Botero,érica C. da Silva,Nelson Luís C. Domingues RSC Adv. 2016 6 27213
7. Galactose-derived phosphonate analogues as potential inhibitors of phosphatidylinositol biosynthesis in mycobacteria
Zoran Dinev,Carlie T. Gannon,Caroline Egan,Jacinta A. Watt,Malcolm J. McConville,Spencer J. Williams Org. Biomol. Chem. 2007 5 952
8. Synthesis of phosphonates: a modified arbuzov procedure
Meng Fang Wang,Martine M. L. Crilley,Bernard T. Golding,Tom McInally,David H. Robinson,Alan Tinker J. Chem. Soc. Chem. Commun. 1991 667
9. The copper-promoted reaction of o-halogenodiarylazo-compounds with nucleophiles. Part 2. The copper-promoted reaction of o-bromodiarylazo-compounds with diesters of phosphorous acid. A novel method for the preparation of dialkyl arylphosphonates
Nigel Hall,Raymond Price J. Chem. Soc. Perkin Trans. 1 1979 2873
10. Phosphorylation of diamines
R. S. Edmundson J. Chem. Soc. C 1971 3614