4443-48-5 ((Bornyl bromide, Pract.)

快速询单

结构式：

Bornyl bromide, Pract.MOL文件

CAS号：

4443-48-5

英文名称：

Bornyl bromide, Pract.

分子式：

C₁₀H₁₇Br

分子量：

217.145982503891

Bornyl bromide, Pract.(4443-48-5)名称与标识符

名称

中文别名：

2-溴硼烷;

英文别名：

Bicyclo[2.2.1]heptane,2-bromo-1,7,7-trimethyl-;BORNYL BROMIDE, PRACT.;BornylBromide;Bornane, 2-bromo-;2-Bromobornanetechnical;2-Bromo-1,7,7-trimethylbicyclo[2.2.1]heptane #;2-Bromobornane;Bornylbromid;2-Bromo-1,7,7-trimethylbicyclo[2.2.1]heptane;MFCD00066594;Bornyl bromide;FT-0623176;DTXSID00963222;SCHEMBL6699644;4443-48-5;OTOQMOVZIUGCQE-UHFFFAOYSA-N;AKOS015836051;DB-080736;

标识符

MDL：

MFCD00066594

InChIKey：

OTOQMOVZIUGCQE-UHFFFAOYSA-N

Inchi：

1S/C10H17Br/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8H,4-6H2,1-3H3

SMILES：

BrC1CC2CCC1(C)C2(C)C

Bornyl bromide, Pract.(4443-48-5)物化性质

实验特性

折射率 : 1.514
沸点 : 208.5°Cat760mmHg
闪点 : 91.4°C
密度 : 1.257

计算特性

精确分子量 : 216.051363
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 : 216.051363
重原子数量 : 11
复杂度 : 185
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 : 3
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） : 4.2
拓扑分子极性表面积 : 0

Bornyl bromide, Pract.(4443-48-5)相关文献

1. Electrochemical reactions. Part XII. Reduction of the 1,3-dibromides, endo-2,endo-6-and exo-2,10-dibromobornane
Azizullah,James Grimshaw J. Chem. Soc. Perkin Trans. 1 1973 425
2. Synthesis of chiral organotin reagents: synthesis of enantiomerically enriched bicyclo[2.2.1]hept-2-yl tin hydrides from camphor. X-Ray crystal structures of (dimethyl)[(1R,2S,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl]tin chloride and methyl(phenyl)bis[(1R,2S,4R)-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl]stannane
Madeleine Helliwell,Eric J. Thomas,Linda A. Townsend J. Chem. Soc. Perkin Trans. 1 2002 1286
3. Mass spectra of dihalogenocycloalkanes
D. S. Ashton,J. M. Tedder,J. C. Walton J. Chem. Soc. B 1970 1775
4. Organic chemistry
P. D. B. de la Mare,T. S. Stevens,J. H. Ridd,Y. Pocker,C. A. Bunton,J. McKenna,A. G. Davies,G. H. Whitham,M. F. Ansell,J. Tedder,A. R. Pinder,J. E. Saxton,W. G. Overend,D. T. Elmore Annu. Rep. Prog. Chem. 1959 56 159
5. Organic chemistry
J. Chem. Soc. Abstr. 1909 96 A281
6. Oxymetallation. Part 16. Modified procedures for reducing peroxymercurials: conversion of non-terminal alkenes into secondary alkyl t-butyl peroxides
A. J. Bloodworth,J. L. Courtneidge J. Chem. Soc. Perkin Trans. 1 1982 1797
7. Organic chemistry
J. Chem. Soc. Abstr. 1922 122 i977
8. Solid-state molecular syntheses: complete reactions without auxiliaries based on the new solid-state mechanism
Gerd Kaupp CrystEngComm 2003 5 117
9. Proceedings of the Chemical Society. September 1964
Proc. Chem. Soc. 1964 273