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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)-

2-chloro-3-nitro-5-(trifluoromethyl)benzamide

NC(=O)c1cc(cc(c1Cl)[N+](=O)[O-])C(F)(F)F Request for Quotation
Chemical Name: 2-chloro-3-nitro-5-(trifluoromethyl)benzamide
CAS Number: 22227-47-0
Product Number: AG00BFB9(AGN-PC-03843K)
Synonyms:
MDL No:
Molecular Formula: C8H4ClF3N2O3
Molecular Weight: 268.5771696

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-3-nitro-5-(trifluoromethyl)benzamide is a versatile compound that finds application in chemical synthesis as a key building block in organic chemistry reactions. This compound serves as a valuable intermediate in the creation of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique structural properties. Its ability to undergo selective transformations, such as reduction, substitution, and functional group interconversion, makes it a crucial component in the production of complex molecules. Additionally, 2-Chloro-3-nitro-5-(trifluoromethyl)benzamide plays a significant role as a substrate in catalytic processes and asymmetric synthesis, enabling the creation of chiral molecules with high efficiency and selectivity. The compound's presence in the synthesis of bioactive compounds and materials further highlights its importance in the realm of modern organic chemistry.