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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)-

Acetic acid, (4-cyanophenoxy)-, methyl ester

COC(=O)COc1ccc(cc1)C#N Request for Quotation
Chemical Name: Acetic acid, (4-cyanophenoxy)-, methyl ester
CAS Number: 272792-14-0
Product Number: AG003RIM(AGN-PC-0K664S)
Synonyms:
MDL No: MFCD05855148
Molecular Formula: C10H9NO3
Molecular Weight: 191.1834

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
191.186g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
191.058g/mol
Monoisotopic Mass:
191.058g/mol
Topological Polar Surface Area:
59.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
235
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl (4-Cyanophenoxy)acetate is a versatile compound widely used in chemical synthesis. Its primary application lies in the field of organic chemistry where it serves as a key building block in the formation of various complex molecules. Through esterification reactions, this compound can be easily incorporated into different organic structures, adding functionality and introducing new chemical properties.In organic synthesis, Methyl (4-Cyanophenoxy)acetate can participate in numerous reactions such as nucleophilic substitution, reduction, and condensation, among others. Its reactive nature allows chemists to manipulate its structure to create custom-designed molecules with specific functions. By selectively modifying the ester group or the cyano group, researchers can tailor the compound for a wide range of applications including pharmaceuticals, agrochemicals, and materials science.Moreover, the presence of the cyanophenoxy moiety in this compound offers opportunities for further derivatization, enabling the synthesis of more complex and diverse molecules. This versatility makes Methyl (4-Cyanophenoxy)acetate a valuable asset in the toolkit of synthetic chemists seeking to develop novel compounds for various industrial and scientific purposes.