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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, 4-methyl-3-nitro-

O=Cc1ccc(c(c1)[N+](=O)[O-])C Request for Quotation
Chemical Name: Benzaldehyde, 4-methyl-3-nitro-
CAS Number: 31680-07-6
Product Number: AG00BXDM(AGN-PC-0K97RI)
Synonyms:
MDL No:
Molecular Formula: C8H7NO3
Molecular Weight: 165.1461

Identification/Properties

Properties
MP:
46-49 °C(lit.)
BP:
276.3°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Stability:
Air Sensitive
Computed Properties
Molecular Weight:
165.148g/mol
XLogP3:
1.9
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Methyl-3-nitrobenzaldehyde, also known as $name$, is a versatile chemical compound widely utilized in chemical synthesis. This compound plays a crucial role in various organic reactions, particularly in the production of pharmaceuticals, agrochemicals, and fine chemicals.One significant application of 4-Methyl-3-nitrobenzaldehyde is its use as a key intermediate in the synthesis of diverse organic compounds. This compound serves as a building block for the preparation of complex molecules, allowing chemists to efficiently construct a range of products with specific functional groups and structures.In addition, 4-Methyl-3-nitrobenzaldehyde is commonly employed in the synthesis of heterocyclic compounds, which are essential in the development of new drugs and materials. By incorporating this compound into the reaction pathways, chemists can access a diverse array of heterocycles with unique properties and applications.Furthermore, 4-Methyl-3-nitrobenzaldehyde is utilized in the manufacturing of dyes and pigments, where its chemical properties contribute to the color and stability of the final products. The compound can undergo various chemical transformations to yield a spectrum of vibrant and robust colorants used in textiles, paints, and other industrial applications.Overall, the versatile nature of 4-Methyl-3-nitrobenzaldehyde makes it a valuable tool in chemical synthesis, enabling the creation of diverse compounds with tailored properties and functionalities.