Silanediamine, hexamethyl-


Chemical Name: Silanediamine, hexamethyl-
CAS Number: 3768-58-9
Product Number: AG003OAO(AGN-PC-0JLQNR)
Synonyms:
MDL No:
Molecular Formula: C6H18N2Si
Molecular Weight: 146.30602

Identification/Properties


Properties
MP:
-98℃
Form:
Liquid
Computed Properties
Molecular Weight:
146.309g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
146.124g/mol
Monoisotopic Mass:
146.124g/mol
Topological Polar Surface Area:
6.5A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
79.1
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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NMR Spectrum


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Chemical Structure



N,N,N′,N′,1,1-Hexamethylsilanediamine, also known as hexamethyldisilazane, is a versatile compound widely used in chemical synthesis. Its primary application lies in the field of organic chemistry, where it serves as a valuable reagent and building block for various reactions.One of the key uses of N,N,N′,N′,1,1-Hexamethylsilanediamine is as a silylating agent. It can be employed to introduce trimethylsilyl (TMS) groups onto molecules, which can serve as protective groups for sensitive functional groups during reactions. By using hexamethyldisilazane, chemists can selectively block certain reactive sites in a molecule while allowing desired transformations to occur elsewhere. This selective silylation strategy is particularly useful in complex synthesis schemes where multiple steps are involved.Furthermore, N,N,N′,N′,1,1-Hexamethylsilanediamine can also act as a deprotecting agent. By utilizing appropriate conditions, TMS groups introduced by hexamethyldisilazane can be efficiently removed, revealing the original functional groups in the molecule. This deprotection step is crucial in the final stages of synthesis when the protected groups are no longer needed.Overall, the versatility of N,N,N′,N′,1,1-Hexamethylsilanediamine in silylation and deprotection reactions makes it a valuable tool in the hands of synthetic chemists. Its ability to modify and protect functional groups selectively contributes significantly to the success of various chemical transformations in organic synthesis.