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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-chloro-2-nitro-

O=Cc1cccc(c1[N+](=O)[O-])Cl Request for Quotation
Chemical Name: Benzaldehyde, 3-chloro-2-nitro-
CAS Number: 22233-52-9
Product Number: AG0033NJ(AGN-PC-0NI8C4)
Synonyms:
MDL No:
Molecular Formula: C7H4ClNO3
Molecular Weight: 185.5646

Identification/Properties

Properties
BP:
313.6±27.0°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
185.563g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
184.988g/mol
Monoisotopic Mass:
184.988g/mol
Topological Polar Surface Area:
62.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
192
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


3-Chloro-2-nitrobenzaldehyde is a versatile chemical compound that finds wide application in organic synthesis processes. It serves as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and dyes. In chemical synthesis, 3-Chloro-2-nitrobenzaldehyde acts as a valuable building block due to its unique structural properties and reactivity.One of the prominent uses of 3-Chloro-2-nitrobenzaldehyde is in the synthesis of complex molecules such as benzimidazoles, which are important heterocyclic compounds with diverse biological activities. This compound can undergo various reactions like nucleophilic substitution, reduction, and condensation to yield a range of derivatives with different functional groups attached.Furthermore, 3-Chloro-2-nitrobenzaldehyde is employed in the preparation of fluorescent dyes and as a starting material for the synthesis of chiral compounds. It participates in cross-coupling reactions and aromatic substitutions to introduce desired substituents onto the benzene ring, allowing for the creation of new chemical entities with tailored properties.Additionally, this compound is utilized in the development of potential drug candidates and in the production of fine chemicals used in the formulation of specialty products. Its versatility and synthetic utility make 3-Chloro-2-nitrobenzaldehyde a valuable asset in the toolkit of organic chemists and researchers working in diverse fields of chemical science.