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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-(4-(Trifluoromethoxy)phenyl)pyrrolidine hydrochloride

FC(Oc1ccc(cc1)C1CCCN1)(F)F.Cl Request for Quotation
Chemical Name: 2-(4-(Trifluoromethoxy)phenyl)pyrrolidine hydrochloride
CAS Number: 1185121-45-2
Product Number: AG008XMU(AGN-PC-0WAM9E)
Synonyms:
MDL No: MFCD08456904
Molecular Formula: C11H13ClF3NO
Molecular Weight: 267.6752

Identification/Properties

Computed Properties
Molecular Weight:
267.676g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
267.064g/mol
Monoisotopic Mass:
267.064g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
224
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
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


The use of 2-(4-(Trifluoromethoxy)phenyl)pyrrolidine hydrochloride in chemical synthesis is prominent in the realm of medicinal chemistry and drug development. This compound serves as a versatile building block for the synthesis of various pharmaceutical agents and organic molecules. Its unique structure containing a trifluoromethoxyphenyl group confers desirable properties such as enhanced lipophilicity and biological activity in the resulting compounds. By incorporating 2-(4-(Trifluoromethoxy)phenyl)pyrrolidine hydrochloride into synthetic routes, chemists can efficiently access a diverse array of novel compounds with potential therapeutic applications.