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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)-

2,4-壬二烯醛

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Chemical Name: 2,4-壬二烯醛
CAS Number: 6750-03-4
Product Number: AG01FZRK(AGN-PC-3H64FM)
Synonyms:
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Molecular Formula:
Molecular Weight:

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Chemical Structure


2,4-Nonadienal, a versatile compound in chemical synthesis, is widely used as a key intermediate in the production of various fragrance and flavor compounds. Known for its distinctive fruity and green odor, 2,4-Nonadienal plays a crucial role in creating the characteristic scents found in perfumes, cosmetics, and food products. Chemically, it is utilized as a building block in the synthesis of aldehydes, alcohols, and carboxylic acids, offering a broad range of applications in the fragrance and flavor industry. Additionally, 2,4-Nonadienal is valued for its role in organic synthesis, serving as a starting material for the preparation of complex molecules and pharmaceutical compounds. Its unique chemical properties make it a valuable component in the creation of diverse products that enhance sensory experiences and contribute to the creation of novel chemical entities.