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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)-

2-Propyn-1-amine, N,N-dimethyl-3-(trimethylsilyl)-

CN(CC#C[Si](C)(C)C)C Request for Quotation
Chemical Name: 2-Propyn-1-amine, N,N-dimethyl-3-(trimethylsilyl)-
CAS Number: 56849-88-8
Product Number: AG00E9WZ(AGN-PC-0KKMKQ)
Synonyms:
MDL No:
Molecular Formula: C8H17NSi
Molecular Weight: 155.31278

Identification/Properties

Computed Properties
Molecular Weight:
155.316g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
155.113g/mol
Monoisotopic Mass:
155.113g/mol
Topological Polar Surface Area:
3.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
153
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-DIMETHYLAMINO-3-(TRIMETHYLSILYL)-2-PROPYNE is a versatile chemical compound commonly used in organic synthesis due to its unique properties and functionalities. This compound, also known by its chemical formula (CH3)3SiC≡CCH2N(CH3)2, plays a crucial role in various chemical transformations and reactions. In chemical synthesis, 1-DIMETHYLAMINO-3-(TRIMETHYLSILYL)-2-PROPYNE is often employed as a reagent in the preparation of alkynes and other organic molecules. It can act as a nucleophilic reagent in reactions with electrophiles, participating in addition reactions to form new carbon-carbon or carbon-heteroatom bonds. Additionally, this compound can undergo deprotonation or deprotection reactions to reveal reactive functional groups for further modification.Furthermore, 1-DIMETHYLAMINO-3-(TRIMETHYLSILYL)-2-PROPYNE is utilized in the synthesis of complex natural products, pharmaceuticals, and materials with tailored properties. Its ability to introduce specific chemical functionalities into target molecules makes it a valuable tool for chemists working in various research fields. Overall, this compound plays a significant role in modern organic chemistry as a versatile building block for creating diverse molecular structures and compounds.