538-60-3 (亚磷酸二苄酯,Dibenzyl Hydrogen Phosphate)

快速询单

结构式：

亚磷酸二苄酯MOL文件

CAS号：

538-60-3

中文名称：

亚磷酸二苄酯

英文名称：

Dibenzyl Hydrogen Phosphate

分子式：

C₁₄H₁₅O₃P

分子量：

262.240864992142

亚磷酸二苄酯(538-60-3)名称与标识符

名称

中文别名：

亚磷酸二苄酯;

英文别名：

Dibenzyl Hydrogen Phosphate;Dibenzyl hydrogen phosphite;DIBENZYL PHOSPHITE;Dibenzyl hydrogen phosphite #;NSC49746;SCHEMBL51153;Phosphorous Acid Dibenzyl Ester;Phosphorous acid, bis(phenylmethyl) ester;538-60-3;DTXSID80871270;DIBENZYLOXYPHOSPHINOUS ACID;Benzyl phosphite (C7H7O)2(HO)P;DYUGVWSETOTNKQ-UHFFFAOYSA-N;AKOS015896399;NSC-49746;

标识符

InChIKey：

DYUGVWSETOTNKQ-UHFFFAOYSA-N

Inchi：

1S/C14H15O3P/c15-18(16-11-13-7-3-1-4-8-13)17-12-14-9-5-2-6-10-14/h1-10,15H,11-12H2

SMILES：

P(O)(OCC1C=CC=CC=1)OCC1C=CC=CC=1

亚磷酸二苄酯(538-60-3)物化性质

实验特性

LogP : 3.63920
PSA : 52.28000
折射率 : n20/D 1.555(lit.)
沸点 : 110-120 °C0.01 mm Hg(lit.)
熔点 : NA
蒸气压 : 0.0±0.9 mmHg at 25°C
闪点 : >230 °F
溶解度 : Chloroform, Ethyl Acetate
颜色与性状 : 淡黄色油状
密度 : 1.187 g/mL at 25 °C(lit.)

计算特性

精确分子量 : 262.07600
氢键供体数量 : 0
氢键受体数量 : 6
可旋转化学键数量 : 11
同位素质量 : 262.076
重原子数量 : 32
复杂度 : 600
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 : 4
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） : 无
互变异构体数量 : 无
表面电荷 : 0
拓扑分子极性表面积 : 38.7A^2

亚磷酸二苄酯(538-60-3)安全信息

WGK Germany： 3
安全说明： H303+H313+H333
危害声明：H303吞入可能有害+H313皮肤接触可能有害+H333吸入可能对身体有害
警示性声明：P264+P280+P305+P351+P338+P337+P313
储存条件： 2-8°C
信号词： warning
FLUKA BRAND F CODES： 21

亚磷酸二苄酯(538-60-3)海关数据

海关编码：

2920901900

海关数据：

中国海关编码：

2920901900

概述：

2920901900 亚磷酸酯。监管条件:无。增值税率:17.0%。退税率:9.0%。最惠国关税:6.5%。普通关税:30.0%

申报要素：

品名, 成分含量, 用途

Summary：

2920901900 VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

亚磷酸二苄酯(538-60-3)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
上海瀚思化工有限公司	18939883912 021-34536277	顾经理	3003949364		询单
上海依赫生物科技有限公司	17721395025 021-68882955	张经理	2423903095		询单

亚磷酸二苄酯(538-60-3)相关文献

1. 176. Studies on phosphorylation. Part V. The reaction of tertiary bases with esters of phosphorous, phosphoric, and pyrophosphoric acids. A new method of selective debenzylation
J. Baddiley,V. M. Clark,J. J. Michalski,A. R. Todd J. Chem. Soc. 1949 815
2. 220. Studies on phosphorylation. Part IV. Further studies on the use of dibenzyl chlorophosphonate and the examination of certain alternative phosphorylation methods
F. R. Atherton,H. T. Howard,A. R. Todd J. Chem. Soc. 1948 1106
3. Fosmidomycin analogues with N-hydroxyimidazole and N-hydroxyimidazolone as a chelating unit
Camille Midrier,Sonia Montel,Ralf Braun,Klaus Haaf,Lothar Willms,Arie van der Lee,Jean-No?l Volle,Jean-Luc Pirat,David Virieux RSC Adv. 2014 4 23770
4. Prodrugs of phosphonoformate: products, kinetics and mechanisms of hydrolysis of dibenzyl (methoxycarbonyl)phosphonate
Antony G. Mitchell,Dave Nicholls,Ian Walker,William J. Irwin,Sally Freeman J. Chem. Soc. Perkin Trans. 2 1991 1297
5. 174. Studies on phosphorylation. Part II. The reaction of dialkyl phosphites with polyhalogen compounds in presence of bases. A new method for the phosphorylation of amines
F. R. Atherton,H. T. Openshaw,A. R. Todd J. Chem. Soc. 1945 660
6. 129. Studies on phosphorylation. Part III. Further observations on the reaction of phosphites with polyhalogen compounds in presence of bases and its application to the phosphorylation of alcohols
F. R. Atherton,A. R. Todd J. Chem. Soc. 1947 674
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 dihydronaphthalene analogues inspired by combretastatin A-4 and their biological evaluation as anticancer agents
Casey J. Maguire,Zhi Chen,Vani P. Mocharla,Madhavi Sriram,Tracy E. Strecker,Ernest Hamel,Heling Zhou,Ramona Lopez,Yifan Wang,Ralph P. Mason,David J. Chaplin,Mary Lynn Trawick,Kevin G. Pinney Med. Chem. Commun. 2018 9 1649
9. 704. Nucleotides. Part XVI. Ribonucleoside-5′ phosphites. A new method for the preparation of mixed secondary phosphites
N. S. Corby,G. W. Kenner,A. R. Todd J. Chem. Soc. 1952 3669
10. 350. Synthesis of quinol monophosphates from vitamin K1, ubiquinone, and other quinones, and experiments on oxidative phosphorylation
K. J. M. Andrews J. Chem. Soc. 1961 1808