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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-Propen-1-ol, 3-phenyl-, propanoate

CCC(=O)OC/C=C/c1ccccc1 Request for Quotation
Chemical Name: 2-Propen-1-ol, 3-phenyl-, propanoate
CAS Number: 103-56-0
Product Number: AG003OWX(AGN-PC-0NVL3H)
Synonyms:
MDL No:
Molecular Formula: C12H14O2
Molecular Weight: 190.2384

Identification/Properties

Properties
BP:
297.4±19.0 °C at 760 mmHg
Storage:
Room Temperature;Keep in dry area;
Computed Properties
Molecular Weight:
190.242g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
5
Exact Mass:
190.099g/mol
Monoisotopic Mass:
190.099g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
191
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
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:
H317
Precautionary Statements:
P261-P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of Cinnamyl propionate in chemical synthesis is primarily as a flavoring agent or fragrance compound. This chemical compound is often used in the pharmaceutical and food industries to provide a sweet, fruity, and floral aroma. In chemical synthesis, Cinnamyl propionate can also serve as a building block for creating more complex organic molecules. Its structure and reactivity make it a valuable starting material for the synthesis of various fragrances, flavors, and even pharmaceutical compounds. The ability of Cinnamyl propionate to undergo various transformations through chemical reactions makes it a versatile compound in the realm of chemical synthesis.