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Trihydrido(1,3,5,7-tetraazatricyclo[3.3.1.13,7]decane-kappaN1)boron, commonly known as H3B-N4, is a boron compound characterized by a distinctive molecular structure. It features a boron atom connected to three hydrogen atoms and a 1,3,5,7-tetraazatricyclo[3.3.1.13,7]decane ligand. trihydrido(1,3,5,7-tetraazatricyclo[3.3.1.1~3,7~]decane-kappaN~1~)boron is of interest in the scientific community due to its potential applications in various chemical processes and material development.

14547-02-5

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14547-02-5 Usage

Uses

Used in Hydrosilation Reactions:
Trihydrido(1,3,5,7-tetraazatricyclo[3.3.1.1~3,7~]decane-kappaN~1~)boron is utilized as a catalyst in hydrosilation reactions, a process that involves the addition of a hydrosilicon (Si-H) bond to unsaturated organic compounds, such as alkenes or alkynes. This reaction is significant in the synthesis of various organosilicon compounds and materials.
Used in Catalysis:
In the field of catalysis, trihydrido(1,3,5,7-tetraazatricyclo[3.3.1.1~3,7~]decane-kappaN~1~)boron is employed as a catalyst to facilitate various chemical reactions. Its unique structure allows it to play a crucial role in enhancing the efficiency and selectivity of catalytic processes.
Used in Hydrogen Storage Materials:
Trihydrido(1,3,5,7-tetraazatricyclo[3.3.1.1~3,7~]decane-kappaN~1~)boron is considered for use in hydrogen storage materials due to its ability to interact with hydrogen atoms. This property makes it a potential candidate for applications in clean energy technologies, such as fuel cells and hydrogen-powered vehicles, where efficient hydrogen storage is essential.
Used in Organic Synthesis:
In organic synthesis, trihydrido(1,3,5,7-tetraazatricyclo[3.3.1.1~3,7~]decane-kappaN~1~)boron is used as a building block or reagent to construct complex organic molecules. Its unique structure and reactivity contribute to the development of new synthetic pathways and the creation of novel organic compounds.
Used in Material Science:
Trihydrido(1,3,5,7-tetraazatricyclo[3.3.1.1~3,7~]decane-kappaN~1~)boron is being studied for its potential use as a building block in the development of new materials. Its unique structure and properties could lead to the creation of advanced materials with applications in various industries, such as electronics, pharmaceuticals, and aerospace.

Check Digit Verification of cas no

The CAS Registry Mumber 14547-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,4 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14547-02:
(7*1)+(6*4)+(5*5)+(4*4)+(3*7)+(2*0)+(1*2)=95
95 % 10 = 5
So 14547-02-5 is a valid CAS Registry Number.

14547-02-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name hexamethylene tetramine monoborane

1.2 Other means of identification

Product number -
Other names Hexamethylentetraminmonoboran

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:14547-02-5 SDS

14547-02-5Relevant articles and documents

Hexamethylenetetramine-borane adducts

Riley, Marvin D.,Miller, Norman E.

, p. 707 - 710 (2008/10/08)

The four possible borane adducts of hexamethylenetetramine (hexamine) were prepared, three of which being hitherto unknown. Synthesis and purification procedures were worked out so that pure samples were available for chemical studies. Pyrolysis of the tetraadduct when controlled proceeded with rearrangement by hydride migration to form dimethylaminoborane derivatives. The adducts were not amenable to borane cation formation; those two cations eventually prepared, (CH2)6N4BH2py+ and (CH2)6N4BH2P(CH3) 3+, were not very stable.

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