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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-methoxy-2-nitro-4-(phenylmethoxy)-

COc1c(OCc2ccccc2)ccc(c1[N+](=O)[O-])C=O Request for Quotation
Chemical Name: Benzaldehyde, 3-methoxy-2-nitro-4-(phenylmethoxy)-
CAS Number: 2450-27-3
Product Number: AG002OD1(AGN-PC-0JSX83)
Synonyms:
MDL No:
Molecular Formula: C15H13NO5
Molecular Weight: 287.2674

Identification/Properties

Properties
MP:
111.5-112.5°C
BP:
487.8±45.0°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
287.271g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
5
Exact Mass:
287.079g/mol
Monoisotopic Mass:
287.079g/mol
Topological Polar Surface Area:
81.4A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
351
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:
H302-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


4-(Benzyloxy)-3-methoxy-2-nitrobenzaldehyde is a versatile compound widely utilized in chemical synthesis. This aldehyde derivative serves as a key building block in the creation of various organic compounds due to its unique molecular structure and reactivity.In chemical synthesis, 4-(Benzyloxy)-3-methoxy-2-nitrobenzaldehyde is commonly employed as a precursor in the preparation of complex molecules such as pharmaceuticals, agrochemicals, and advanced materials. Its nitro and aldehyde functional groups allow for versatile transformations, making it a valuable intermediate in organic synthesis.This compound can undergo various chemical reactions, including reduction, condensation, and substitution reactions, to yield a range of products with tailored properties. The benzyloxy and methoxy groups in the molecule provide opportunities for selective modifications and controlled functionalization, enabling chemists to design and synthesize diverse molecular structures.Overall, the strategic use of 4-(Benzyloxy)-3-methoxy-2-nitrobenzaldehyde in chemical synthesis offers a pathway to access intricate organic compounds with precise control over structure and functionality, facilitating the development of novel materials and bioactive molecules.