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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)-

Benzene, 1-nitro-4-(trifluoromethoxy)-

FC(Oc1ccc(cc1)[N+](=O)[O-])(F)F Request for Quotation
Chemical Name: Benzene, 1-nitro-4-(trifluoromethoxy)-
CAS Number: 713-65-5
Product Number: AG003KB6(AGN-PC-0JSAL5)
Synonyms:
MDL No:
Molecular Formula: C7H4F3NO3
Molecular Weight: 207.1068

Identification/Properties

Properties
MP:
15 °C
BP:
217.4°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
1.467
Computed Properties
Molecular Weight:
207.108g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
207.014g/mol
Monoisotopic Mass:
207.014g/mol
Topological Polar Surface Area:
55A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
205
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


1-Nitro-4-(trifluoromethoxy)benzene, also known as NTB, is a versatile compound widely used in chemical synthesis. With its unique structure and reactivity, NTB plays a crucial role in the preparation of various organic molecules and materials. In chemical synthesis, 1-Nitro-4-(trifluoromethoxy)benzene is commonly employed as a key building block for the creation of complex aromatic compounds. Its nitro group provides a useful handle for further derivatization, allowing chemists to introduce a wide range of functional groups and modifications. Additionally, the presence of the trifluoromethoxy moiety enhances the compound's reaction profile, enabling selective and efficient transformations in organic reactions.One of the main applications of NTB in chemical synthesis is its utility as a precursor for the synthesis of pharmaceutical compounds and agrochemicals. By strategically incorporating 1-Nitro-4-(trifluoromethoxy)benzene into synthetic routes, researchers can access novel drug candidates with improved biological activities and pharmacokinetic properties. Moreover, NTB serves as a valuable intermediate in the preparation of specialty chemicals, polymers, and advanced materials with tailored properties.Overall, the versatility and synthetic utility of 1-Nitro-4-(trifluoromethoxy)benzene make it a valuable tool in modern organic synthesis, enabling the construction of diverse molecular architectures and facilitating the development of innovative compounds for various industrial applications.