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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)-

Benzoic acid, 3-chloro-5-nitro-

Clc1cc(cc(c1)C(=O)O)[N+](=O)[O-] Request for Quotation
Chemical Name: Benzoic acid, 3-chloro-5-nitro-
CAS Number: 34662-36-7
Product Number: AG003J9L(AGN-PC-0JNAWK)
Synonyms:
MDL No: MFCD09263224
Molecular Formula: C7H4ClNO4
Molecular Weight: 201.5640

Identification/Properties

Properties
BP:
351.1°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
201.562g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
200.983g/mol
Monoisotopic Mass:
200.983g/mol
Topological Polar Surface Area:
83.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
227
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Chloro-5-nitro-benzoic acid, also known as $name$, is a versatile chemical compound widely used in chemical synthesis. One key application of this compound is in the production of various pharmaceuticals and agrochemicals. It serves as a crucial intermediate in the synthesis of a range of important compounds due to its unique properties and reactivity.In chemical synthesis, 3-Chloro-5-nitro-benzoic acid is often used as a building block for creating more complex molecules. Its chloro and nitro functional groups make it a valuable precursor for introducing specific functional groups into the target molecules. This compound can undergo a variety of chemical reactions, such as nucleophilic substitution, reduction, and coupling reactions, to yield diverse products with desired properties.Additionally, 3-Chloro-5-nitro-benzoic acid is employed in the development of new materials, dyes, and catalysts. Its versatility in chemical transformations makes it an essential component in the toolbox of synthetic chemists for designing and synthesizing novel compounds with potential applications in various industries.Overall, the application of 3-Chloro-5-nitro-benzoic acid in chemical synthesis underscores its significance as a key building block for creating valuable compounds with diverse functionalities and applications in the fields of pharmaceuticals, agrochemicals, materials science, and more.