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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)-

Butanal, 3-methyl-2-(1-methylethyl)-

O=CC(C(C)C)C(C)C Request for Quotation
Chemical Name: Butanal, 3-methyl-2-(1-methylethyl)-
CAS Number: 35155-64-7
Product Number: AG01B9E1(AGN-PC-0NJ7RI)
Synonyms:
MDL No:
Molecular Formula: C8H16O
Molecular Weight: 128.2120

Identification/Properties

Computed Properties
Molecular Weight:
128.215g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
128.12g/mol
Monoisotopic Mass:
128.12g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
76.6
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


3-Methyl-2-(propan-2-yl)butanal, also known as $name$, is a versatile compound commonly used in chemical synthesis for its unique properties and reactions. This aldehyde serves as a valuable building block in the creation of various organic compounds due to its distinct chemical structure and reactivity.In chemical synthesis, $name$ plays a crucial role as a precursor in the production of complex molecules such as pharmaceuticals, fragrances, and fine chemicals. Its branched structure with a methyl and isopropyl group enables it to participate in a range of reactions, including aldol condensation, Grignard reactions, and Wittig reactions, leading to the formation of diverse derivatives.One key application of 3-Methyl-2-(propan-2-yl)butanal is its involvement in the synthesis of chiral auxiliary compounds used in asymmetric synthesis. By leveraging its stereochemical properties, chemists can efficiently access enantiomerically pure building blocks, facilitating the creation of stereoselective molecules with high precision and efficacy.Furthermore, this compound serves as a valuable starting material for the preparation of complex natural products and drug intermediates, highlighting its significance in the pharmaceutical and chemical industries. Its ability to undergo diverse transformations and functional group manipulations makes it a versatile tool for organic chemists seeking to design and synthesize novel molecules with specific properties and functionalities.Overall, 3-Methyl-2-(propan-2-yl)butanal is a fundamental component in the toolkit of synthetic chemists, enabling the efficient construction of intricate organic structures and providing a pathway to diverse chemical innovations and discoveries in the field of organic chemistry.