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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)-

1-Propanamine, 3-[3,3,3-trimethyl-1,1-bis[(trimethylsilyl)oxy]disiloxanyl]-

NCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)O[Si](C)(C)C Request for Quotation
Chemical Name: 1-Propanamine, 3-[3,3,3-trimethyl-1,1-bis[(trimethylsilyl)oxy]disiloxanyl]-
CAS Number: 25357-81-7
Product Number: AG00BC0L(AGN-PC-0KKL4Y)
Synonyms:
MDL No:
Molecular Formula: C12H35NO3Si4
Molecular Weight: 353.7532

Identification/Properties

Computed Properties
Molecular Weight:
353.756g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
9
Exact Mass:
353.169g/mol
Monoisotopic Mass:
353.169g/mol
Topological Polar Surface Area:
53.7A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
254
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:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


$Name$ is a versatile chemical compound that finds significant application in chemical synthesis processes. Its unique structure, consisting of a trisiloxane backbone and a propylamine functional group, imparts distinctive properties that make it a valuable reagent in various synthetic reactions. One key application of 3-(1,1,1,5,5,5-Hexamethyl-3-((trimethylsilyl)oxy)trisiloxan-3-yl)propan-1-amine is as a silylating agent in organic synthesis. The trimethylsilyl group attached to the trisiloxane scaffold enables selective silylation of hydroxyl or amino groups in organic molecules. This silylation reaction is particularly useful in protecting sensitive functional groups during multi-step synthesis, preventing unwanted side reactions and enhancing overall yield.Additionally, $Name$ can act as a cross-linking agent in polymer chemistry. The trisiloxane backbone confers flexibility and stability, making it suitable for creating durable polymer networks through cross-linking reactions. This property is exploited in the production of functional materials such as coatings, adhesives, and sealants where robustness and chemical resistance are desired.Furthermore, the propylamine moiety in $Name$ can serve as a precursor for introducing nitrogen-containing groups into organic molecules. This functionality is valuable in medicinal chemistry for the synthesis of bioactive compounds, as well as in materials science for imparting specific properties such as improved adhesion or corrosion resistance.In conclusion, the application of 3-(1,1,1,5,5,5-Hexamethyl-3-((trimethylsilyl)oxy)trisiloxan-3-yl)propan-1-amine in chemical synthesis spans a wide range of industries, offering tailored solutions for complex synthetic challenges and enabling the development of innovative materials and compounds.