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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)-

3-Butyn-2-ol, 2-methyl-4-(trimethylsilyl)-

C[Si](C#CC(O)(C)C)(C)C Request for Quotation
Chemical Name: 3-Butyn-2-ol, 2-methyl-4-(trimethylsilyl)-
CAS Number: 5272-33-3
Product Number: AG00DEID(AGN-PC-0JM8S9)
Synonyms:
MDL No:
Molecular Formula: C8H16OSi
Molecular Weight: 156.2975

Identification/Properties

Properties
MP:
42 °C
BP:
186.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Refractive Index:
1.467 (589.3 nm 20℃)
Computed Properties
Molecular Weight:
156.3g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
156.097g/mol
Monoisotopic Mass:
156.097g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
174
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


2-Methyl-4-(trimethylsilyl)but-3-yn-2-ol, also known as $name$, is a versatile compound commonly used in organic synthesis. This compound serves as a valuable building block in the field of chemical synthesis due to its unique structural properties and reactivity. 2-Methyl-4-(trimethylsilyl)but-3-yn-2-ol plays a crucial role in alkyne chemistry, where it can undergo various transformations to yield functionalized organic molecules. In chemical synthesis, this compound is often employed as a synthetic intermediate in the preparation of complex organic compounds. Its triple bond and silyl group provide opportunities for selective functionalization, making it a valuable tool for chemists working on the synthesis of pharmaceuticals, agrochemicals, and materials. Additionally, the presence of the trimethylsilyl group offers protection for sensitive functional groups during synthetic pathways, allowing for controlled reactions and enhanced yields.Furthermore, 2-Methyl-4-(trimethylsilyl)but-3-yn-2-ol can participate in transition metal-catalyzed cross-coupling reactions, Sonogashira couplings, and other transformations to introduce specific functionalities into target molecules. Its incorporation into molecular structures can lead to the formation of diverse compounds with varied properties and applications in the chemical industry.