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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)-

Benzenemethanamine, 4-(difluoromethoxy)-

NCc1ccc(cc1)OC(F)F Request for Quotation
Chemical Name: Benzenemethanamine, 4-(difluoromethoxy)-
CAS Number: 177842-14-7
Product Number: AG0025KV(AGN-PC-0KBPDU)
Synonyms:
MDL No:
Molecular Formula: C8H9F2NO
Molecular Weight: 173.1600

Identification/Properties

Properties
BP:
227.3°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Stability:
Air Sensitive
Refractive Index:
1.491
Computed Properties
Molecular Weight:
173.163g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
173.065g/mol
Monoisotopic Mass:
173.065g/mol
Topological Polar Surface Area:
35.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
124
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:
Danger
UN#:
2735
Hazard Statements:
H314-H318
Precautionary Statements:
P280-P301+P330+P331-P302+P352-P304+P340-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Difluoromethoxy)benzenemethanamine is a versatile compound that finds widespread application in chemical synthesis. This compound serves as a valuable building block for the creation of various pharmaceuticals, agrochemicals, and materials. Its unique chemical structure containing a difluoromethoxy group provides enhanced reactivity and selectivity in a range of reactions.In medicinal chemistry, 4-(Difluoromethoxy)benzenemethanamine is commonly utilized for the synthesis of novel drug candidates due to its ability to introduce specific functional groups and enhance biological activity. With its fluorine-containing moiety, this compound can help improve drug efficacy, metabolic stability, and pharmacokinetic properties.Furthermore, in the field of agrochemicals, this compound serves as a key intermediate for developing pesticides and herbicides with improved performance and environmental safety. The difluoromethoxy group in 4-(Difluoromethoxy)benzenemethanamine can impart desirable physicochemical properties to the final products, making them more effective in pest control and crop protection.In material science, the incorporation of 4-(Difluoromethoxy)benzenemethanamine in polymer synthesis can lead to the production of innovative materials with advanced properties such as increased thermal stability, chemical resistance, and optical characteristics. This compound can act as a modifier to tailor the physical and chemical properties of polymers for various industrial applications.Overall, the application of 4-(Difluoromethoxy)benzenemethanamine in chemical synthesis plays a crucial role in the development of diverse compounds with enhanced functionality and performance across pharmaceuticals, agrochemicals, and materials sectors.