1. Home
  2. Silanamine, 1,1'-(1,2-ethanediyl)bis[N,N,1,1-tetramethyl-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Silanamine, 1,1'-(1,2-ethanediyl)bis[N,N,1,1-tetramethyl-

CN([Si](CC[Si](N(C)C)(C)C)(C)C)C Request for Quotation
Chemical Name: Silanamine, 1,1'-(1,2-ethanediyl)bis[N,N,1,1-tetramethyl-
CAS Number: 91166-50-6
Product Number: AG003DD2(AGN-PC-0L6V21)
Synonyms:
MDL No:
Molecular Formula: C10H28N2Si2
Molecular Weight: 232.51372

Identification/Properties

Properties
Form:
Liquid
Computed Properties
Molecular Weight:
232.518g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
5
Exact Mass:
232.179g/mol
Monoisotopic Mass:
232.179g/mol
Topological Polar Surface Area:
6.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
157
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

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
2924
Hazard Statements:
H225-H314
Precautionary Statements:
P210-P280-P305+P351+P338-P310
Class:
3,8
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


1,2-Bis[(dimethylamino)dimethylsilyl]ethane, also known as $name$, is a versatile compound widely used in chemical synthesis as a strong nucleophile and a Lewis base. Its unique structure, containing both amino and silyl groups, allows it to participate in a variety of reactions, making it a valuable tool in organic chemistry.In chemical synthesis, $name$ is commonly employed as a reagent for the functionalization of organic molecules. Its nucleophilic nature allows it to react with electrophiles, facilitating the formation of new carbon-carbon or carbon-heteroatom bonds. This makes it particularly useful in the construction of complex organic molecules, such as pharmaceuticals and agrochemicals.Additionally, $name$ can also act as a chelating agent due to the presence of the silyl groups, which can coordinate with transition metal ions. This property enables it to enhance the reactivity and selectivity of metal-catalyzed reactions, leading to more efficient synthetic pathways.Overall, the strategic use of 1,2-Bis[(dimethylamino)dimethylsilyl]ethane in chemical synthesis offers synthetic chemists a powerful tool for the efficient and controlled formation of diverse chemical bonds, contributing to the development of novel molecules with a wide range of potential applications.