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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)-

Benzenamine, 2-chloro-6-methyl-4-nitro-

Cc1cc(cc(c1N)Cl)[N+](=O)[O-] Request for Quotation
Chemical Name: Benzenamine, 2-chloro-6-methyl-4-nitro-
CAS Number: 69951-02-6
Product Number: AG003B7G(AGN-PC-0KK62H)
Synonyms:
MDL No:
Molecular Formula: C7H7ClN2O2
Molecular Weight: 186.5957

Identification/Properties

Properties
MP:
170-175 °C
BP:
344.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Refractive Index:
1.5560 (estimate)
Computed Properties
Molecular Weight:
186.595g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
186.02g/mol
Monoisotopic Mass:
186.02g/mol
Topological Polar Surface Area:
71.8A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
183
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:
H317-H319
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-Chloro-6-methyl-4-nitroaniline is a versatile intermediate compound commonly used in chemical synthesis. Its application lies primarily in its role as a building block for the creation of various organic compounds. Due to its specific chemical structure, this compound can participate in a range of reactions, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and dyes. Additionally, 2-Chloro-6-methyl-4-nitroaniline can be utilized as a precursor in the preparation of heterocyclic compounds and other complex organic molecules. Its selective reactivity and ability to introduce specific functional groups make it a crucial component in the toolkit of organic chemists seeking to design and produce novel chemical entities.