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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)-

6-(Trifluoromethoxy)indoline

FC(Oc1ccc2c(c1)NCC2)(F)F Request for Quotation
Chemical Name: 6-(Trifluoromethoxy)indoline
CAS Number: 959235-95-1
Product Number: AG0035Y1(AGN-PC-0WAJZU)
Synonyms:
MDL No:
Molecular Formula: C9H8F3NO
Molecular Weight: 203.1611

Identification/Properties

Properties
BP:
223.3±40.0°C at N/A mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
203.164g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
203.056g/mol
Monoisotopic Mass:
203.056g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
207
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-(Trifluoromethoxy)indoline is a versatile compound widely used in chemical synthesis for its unique properties. This compound serves as a valuable building block in the creation of various organic molecules and pharmaceuticals. Its trifluoromethoxy group provides enhanced stability and reactivity, making it an ideal reagent in the formation of complex structures. In addition, the indoline moiety in this compound offers opportunities for diversification through functional group transformations, enabling the synthesis of a wide range of intricate organic compounds. Due to its significance in modern synthetic chemistry, 6-(Trifluoromethoxy)indoline plays a crucial role in the development of novel materials and bioactive compounds with potential applications in pharmaceuticals, agrochemicals, and materials science.