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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)-

Propanoic acid, 3-(2-chlorophenoxy)-

OC(=O)CCOc1ccccc1Cl Request for Quotation
Chemical Name: Propanoic acid, 3-(2-chlorophenoxy)-
CAS Number: 7170-45-8
Product Number: AG0063GK(AGN-PC-0JLTCT)
Synonyms:
MDL No:
Molecular Formula: C9H9ClO3
Molecular Weight: 200.6190

Identification/Properties

Properties
MP:
108-109℃
BP:
305.6°Cat760mmHg
Storage:
Room Temperature;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
200.618g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
200.024g/mol
Monoisotopic Mass:
200.024g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
172
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(2-Chlorophenoxy)propanoic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. Its application in organic chemistry is particularly significant in the production of herbicides and plant growth regulators. The strategic incorporation of the 2-chlorophenoxy functional group enables $name$ to serve as a key building block in the creation of various organic compounds with herbicidal properties. By leveraging the reactivity of the carboxylic acid group and the aromatic chloride moiety, chemists can efficiently modify and functionalize $name$ to tailor its chemical properties for specific application needs. With its prominent role in the synthesis of herbicides, 3-(2-Chlorophenoxy)propanoic acid plays a crucial part in the development of sustainable agricultural solutions and the advancement of crop protection technologies.