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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)-

Benzaldehyde, 3-(1-methylethyl)-

O=Cc1cccc(c1)C(C)C Request for Quotation
Chemical Name: Benzaldehyde, 3-(1-methylethyl)-
CAS Number: 34246-57-6
Product Number: AG007H12(AGN-PC-0JS9LY)
Synonyms:
MDL No: MFCD08062435
Molecular Formula: C10H12O
Molecular Weight: 148.2017

Identification/Properties

Computed Properties
Molecular Weight:
148.205g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
148.089g/mol
Monoisotopic Mass:
148.089g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
129
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-Isopropylbenzaldehyde, also known as IPA, is a versatile compound widely utilized in chemical synthesis. This aromatic aldehyde is valued for its unique properties that make it a crucial intermediate in various reactions and processes. In the realm of organic chemistry, 3-Isopropylbenzaldehyde serves as a key building block for the synthesis of diverse compounds, including pharmaceuticals, fragrances, and agrochemicals. Its functional groups and reactivity make it an invaluable tool for chemists looking to introduce specific structural motifs in their target molecules. Additionally, 3-Isopropylbenzaldehyde finds application in the preparation of advanced materials and fine chemicals due to its ability to participate in a range of transformations, such as condensations, reductions, and functional group modifications. Chemists rely on this compound for its versatility and reliability in enabling the synthesis of a wide array of valuable products.