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5-(4-bromophenyl)-4,6,11-trioxa-1-aza-5-silabicyclo[3.3.3]undecane is a complex organic compound with the molecular formula C11H16BrNO3Si. It features a unique structure, consisting of a bicyclo[3.3.3]undecane core with a nitrogen atom, three oxygen atoms, and a silicon atom. The compound is characterized by the presence of a 4-bromophenyl group attached to the nitrogen atom, which contributes to its chemical properties. 5-(4-bromophenyl)-4,6,11-trioxa-1-aza-5-silabicyclo[3.3.3]undecane is of interest in the field of organic chemistry, particularly in the synthesis of various pharmaceuticals and materials due to its potential reactivity and unique structural features.

86806-91-9

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86806-91-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86806-91-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,8,0 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 86806-91:
(7*8)+(6*6)+(5*8)+(4*0)+(3*6)+(2*9)+(1*1)=169
169 % 10 = 9
So 86806-91-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H16BrNO3Si/c13-11-1-3-12(4-2-11)18-15-8-5-14(6-9-16-18)7-10-17-18/h1-4H,5-10H2

86806-91-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-bromophenyl)-4,6,11-trioxa-1-aza-5-silabicyclo[3.3.3]undecane

1.2 Other means of identification

Product number -
Other names 1-(4-Bromophenyl)-2,8,9-trioxa-5-aza-1-silabicyclo(3.3.3)undecane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:86806-91-9 SDS

86806-91-9Downstream Products

86806-91-9Relevant academic research and scientific papers

The crystal structure of 1-p-bromophenylsilatrane at 293 K and 133 K

Parkanyi,Kertesz,Bihatsi,Hencsei

, p. 153 - 158 (1996)

The crystal structure of 1-p-bromophenylsilatrane was determined at ambient and low temperature. The methylene groups of the silatrane skeleton in the β-position to the nitrogen atom are disordered in the ambient temperature structure. The disorder disappears at 133 K. The Si mutually implies N dative bond length is nearly identical at both temperatures (2.139(3) and 2.132(2) A). The deviation of the atoms in the silatrane moiety from the ideal three-fold symmetry seems to point to the most dynamically behaving parts of the molecule.

Organosilatrane building blocks

Brennan, Bradley J.,Gust, Devens,Brudvig, Gary W.

, p. 1062 - 1064 (2014/02/14)

Phenylsilatrane analogues containing reactive amino, bromo, boronic ester, and alkynyl functional groups for coupling reactions have been prepared. Pinacol boronic ester and ethynyl analogues were synthesized from 4- bromophenylsilatrane by palladium cata

Organosilatrane building blocks

Brennan, Bradley J.,Gust, Devens,Brudvig, Gary W.

, p. 1062 - 1064 (2015/02/19)

Phenylsilatrane analogues containing reactive amino, bromo, boronic ester, and alkynyl functional groups for coupling reactions have been prepared. Pinacol boronic ester and ethynyl analogues were synthesized from 4-bromophenylsilatrane by palladium catal

Synthesis of organosilatranes via rhodium(I)-catalyzed silylation of organic iodides with hydrosilatrane

Murata, Miki,Yamasaki, Hiroyuki,Uogishi, Kota,Watanabe, Shinji,Masuda, Yuzuru

, p. 2944 - 2946 (2008/03/13)

The silylation of aryl and alkenyl iodides with hydrosilatrane in the presence of a rhodium(I) catalyst and DABCO provides the corresponding organosilatranes in good yield. The same catalyst system also enables the related coupling of hydrogermatrane. Georg Thieme Verlag Stuttgart.

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