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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-Propenal, 3-(2-methylphenyl)-, (2E)-

O=C/C=C/c1ccccc1C Request for Quotation
Chemical Name: 2-Propenal, 3-(2-methylphenyl)-, (2E)-
CAS Number: 93614-78-9
Product Number: AG00GRN6(AGN-PC-0ONOEC)
Synonyms:
MDL No:
Molecular Formula: C10H10O
Molecular Weight: 146.1858

Identification/Properties

Properties
BP:
259.691 °C at 760 mmHg

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 3-(o-Tolyl)acrylaldehyde is a versatile compound commonly utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a crucial building block in organic chemistry, particularly in the formation of various functionalized molecules. Its specific application lies in its ability to participate in a range of highly valuable reactions, such as the Horner–Wadsworth–Emmons reaction, which is utilized for the synthesis of olefins. Additionally, 3-(o-Tolyl)acrylaldehyde can be employed as a key intermediate in the production of pharmaceuticals, agrochemicals, and materials with advanced functionalities. Its structural features and reactivity make it an indispensable tool for synthetic chemists seeking to design and create complex organic molecules with precision and efficiency.