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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-methyl-5-nitro-

O=Cc1cc(ccc1C)[N+](=O)[O-] Request for Quotation
Chemical Name: Benzaldehyde, 2-methyl-5-nitro-
CAS Number: 16634-91-6
Product Number: AG001WNU(AGN-PC-0NJRSL)
Synonyms:
MDL No:
Molecular Formula: C8H7NO3
Molecular Weight: 165.1461

Identification/Properties

Computed Properties
Molecular Weight:
165.148g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
165.043g/mol
Monoisotopic Mass:
165.043g/mol
Topological Polar Surface Area:
62.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
187
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Methyl-5-nitrobenzaldehyde, a versatile chemical compound, holds a pivotal role in chemical synthesis due to its unique properties. This compound is commonly used as a key building block in the synthesis of various organic compounds, especially in the field of medicinal chemistry. 2-Methyl-5-nitrobenzaldehyde serves as a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and fine chemicals. Its nitro group makes it a useful precursor for the synthesis of diverse heterocyclic compounds, which have significant applications in drug discovery and development. Additionally, the aldehyde functionality in 2-Methyl-5-nitrobenzaldehyde allows for further functionalization through various chemical reactions, enabling the synthesis of complex molecules with specific desired properties. Due to its importance in chemical synthesis, 2-Methyl-5-nitrobenzaldehyde is a crucial tool for chemists and researchers striving to develop novel compounds with potential applications in various industries.