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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, (2,3-dichlorophenoxy)-

OC(=O)COc1cccc(c1Cl)Cl Request for Quotation
Chemical Name: Acetic acid, (2,3-dichlorophenoxy)-
CAS Number: 2976-74-1
Product Number: AG002ZBQ(AGN-PC-0JKDVO)
Synonyms:
MDL No:
Molecular Formula: C8H6Cl2O3
Molecular Weight: 221.0374

Identification/Properties

Properties
MP:
172-175 °C
BP:
348.4 °C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
221.033g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
219.969g/mol
Monoisotopic Mass:
219.969g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
186
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,3-Dichlorophenoxyacetic acid, also known as 2,3-D, is a powerful synthetic auxin that is commonly used in chemical synthesis processes. Its main application lies in its role as a plant hormone mimic, allowing researchers to manipulate plant growth and development in controlled settings. In chemical synthesis, 2,3-D serves as a valuable reagent for the preparation of various organic compounds due to its ability to induce cell elongation and division in plants, which can be translated into enhanced synthesis and production of desired compounds. This versatile compound plays a crucial role in promoting specific physiological responses in plants, making it an indispensable tool for chemists and researchers alike.