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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)-

Heptanal, 3-ethyl-

CCCCC(CC=O)CC Request for Quotation
Chemical Name: Heptanal, 3-ethyl-
CAS Number: 2570-97-0
Product Number: AG01A39I(AGN-PC-00BDZ1)
Synonyms:
MDL No:
Molecular Formula: C9H18O
Molecular Weight: 142.2386

Identification/Properties

Computed Properties
Molecular Weight:
142.242g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
6
Exact Mass:
142.136g/mol
Monoisotopic Mass:
142.136g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
78.8
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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-Ethylheptanal is a vital component in chemical synthesis, commonly utilized as a versatile building block in the creation of various compounds. In organic chemistry, it serves as a key precursor in the synthesis of aldehydes, ketones, and alcohols through a range of chemical reactions such as oxidation, reduction, and condensation. Its strategic placement of functional groups makes it a valuable intermediate for the production of pharmaceuticals, fragrances, and fine chemicals. Additionally, 3-Ethylheptanal is employed as a reagent in the preparation of complex organic molecules, enabling chemists to access diverse structural motifs for further exploration and development in the realms of drug discovery and material science. Its unique molecular structure and reactivity offer researchers a powerful tool for the advancement of modern chemical synthesis techniques.