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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, 2-methoxy-4-methyl-

COc1cc(C)ccc1C=O Request for Quotation
Chemical Name: Benzaldehyde, 2-methoxy-4-methyl-
CAS Number: 57415-35-7
Product Number: AG003HIW(AGN-PC-0LTCAD)
Synonyms:
MDL No: MFCD06248007
Molecular Formula: C9H10O2
Molecular Weight: 150.1745

Identification/Properties

Properties
MP:
40-43 °C
BP:
258°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
150.177g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
150.068g/mol
Monoisotopic Mass:
150.068g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
134
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Methoxy-4-methylbenzaldehyde, also known as veratraldehyde, is a versatile chemical compound that finds wide applications in chemical synthesis. One of the key uses of this compound is its role as a building block in the synthesis of various pharmaceuticals, agrochemicals, and fragrances. In organic synthesis, 2-Methoxy-4-methylbenzaldehyde serves as a vital intermediate in the production of numerous organic compounds due to its aromatic nature and reactivity. Its aldehyde functional group allows for the formation of important carbon-carbon and carbon-oxygen bonds, enabling the creation of complex molecular structures. Additionally, this compound is utilized in the preparation of flavor and fragrance ingredients, where its unique aromatic profile adds depth and complexity to end products. Its versatility and importance as a starting material make 2-Methoxy-4-methylbenzaldehyde a valuable component in the toolbox of synthetic chemists across various industries.