14500-82-4 ((Phosphinous bromide(6CI,8CI,9CI))

快速询单

结构式：

Phosphinous bromide(6CI,8CI,9CI)MOL文件

CAS号：

14500-82-4

英文名称：

Phosphinous bromide(6CI,8CI,9CI)

分子式：

BrH₂P

分子量：

112.893640041351

Phosphinous bromide(6CI,8CI,9CI)(14500-82-4)名称与标识符

名称

英文别名：

Phosphinous bromide(6CI,8CI,9CI);bromophosphane;Bromophosphine;Phosphine, bromo-;Phosphinous bromide;DTXSID10592648;14500-82-4;

标识符

InChIKey：

IJJURYQDEVNZCW-UHFFFAOYSA-N

Inchi：

1S/BrH2P/c1-2/h2H2

SMILES：

BrP

Phosphinous bromide(6CI,8CI,9CI)(14500-82-4)物化性质

实验特性

LogP : 1.17140
PSA : 0

计算特性

精确分子量 : 111.90776
氢键供体数量 : 0
氢键受体数量 : 0
可旋转化学键数量 : 0
同位素质量 : 111.90775g/mol
重原子数量 : 2
复杂度 : 2
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
拓扑分子极性表面积 : 0Å²

Phosphinous bromide(6CI,8CI,9CI)(14500-82-4)相关文献

1. Facile synthesis and nematicidal activity evaluation of thiophosphinyl amide [(Pz)2P(S)NHR] and thiophosphonyl diamide [(Pz)P(S)(NHR)2] (Pz = 1,3,5-trimethylpyrazole, R = biphenyl derivatives)
Xiao Chen,Xiaogang Lu,Haibo Liu,Hongmei Wang,Chengxin Pei RSC Adv. 2021 11 36250
2. Phosphorus–fluorine chemistry. Part XXI. Pentafluorophenylfluorophosphines and pentafluorophenylfluorophosphoranes
M. Fild,R. Schmutzler J. Chem. Soc. A 1969 840
3. Synthesis and characterisation of novel o-xylene-based P,E ligands
Kathryn M. Allan,John L. Spencer Org. Biomol. Chem. 2014 12 956
4. Stereoselective addition of Grignard reagents to new P-chirogenic N-phosphinoylimines
Irene Notar Francesco,Alain Wagner,Fran?oise Colobert Chem. Commun. 2010 46 2139
5. Versatile routes to selenoether functionalised tertiary phosphines
Tom J. Cunningham,Mark R. J. Elsegood,Paul F. Kelly,Martin B. Smith,Paul M. Staniland Dalton Trans. 2010 39 5216
6. Recent advances in Sonogashira reactions
Rafael Chinchilla,Carmen Nájera Chem. Soc. Rev. 2011 40 5084
7. Palladium(ii) complexes with chelating N-phosphanyl acyclic diaminocarbenes: synthesis, characterization and catalytic performance in Suzuki couplings
Anatoliy Marchenko,Georgyi Koidan,Anastasiya Hurieva,Yurii Vlasenko,Aleksandr Kostyuk,Andrea Biffis Dalton Trans. 2016 45 1967
8. Electrophilic terminal phosphinidene complex–Lewis base adducts: Chemistry between carbon–halide bond activation and weak Lewis base adduct formation
Arif Ali Khan,Cathleen Wismach,Peter G. Jones,Rainer Streubel Chem. Commun. 2003 2892
9. Coupling of ortho-substituted aryl chlorides with bulky amides
Florian C. Falk,Roland Fr?hlich,Jan Paradies Chem. Commun. 2011 47 11095
10. A comprehensive review of caged phosphines: synthesis, catalytic applications, and future perspectives
Harshita Shet,Udaysinh Parmar,Shatrughn Bhilare,Anant R. Kapdi Org. Chem. Front. 2021 8 1599