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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)-

Propane, 1,1,1-trifluoro-3-iodo-

ICCC(F)(F)F Request for Quotation
Chemical Name: Propane, 1,1,1-trifluoro-3-iodo-
CAS Number: 460-37-7
Product Number: AG0032SE(AGN-PC-0JPKTX)
Synonyms:
MDL No:
Molecular Formula: C3H4F3I
Molecular Weight: 223.9635

Identification/Properties

Properties
BP:
90°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Stability:
Light Sensitive
Refractive Index:
n20/D 1.42(lit.)
Computed Properties
Molecular Weight:
223.965g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
223.931g/mol
Monoisotopic Mass:
223.931g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
48.6
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P280-P302+P352-P305+P351+P338-P261
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Iodo-3,3,3-Trifluoropropane, also known as trifluoroiodomethane, is a versatile compound widely used in chemical synthesis. This compound is highly valued for its unique reactivity and ability to introduce the trifluoromethyl group into organic molecules. In the field of medicinal chemistry, 1-Iodo-3,3,3-Trifluoropropane is often employed as a synthetic building block in the creation of pharmaceuticals and agrochemicals. Its trifluoromethyl group can significantly enhance the biological activity and metabolic stability of the resulting compounds, making it a valuable tool for drug discovery. Additionally, this compound is utilized in the modification of materials and polymers, where the trifluoromethyl moiety can impart desirable properties such as increased hydrophobicity and thermal stability. Furthermore, 1-Iodo-3,3,3-Trifluoropropane plays a crucial role in the development of advanced materials, catalysts, and specialty chemicals due to its unique chemical structure and reactivity profile.