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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, (naphthalenyloxy)-

OC(=O)COc1cccc2c1cccc2 Request for Quotation
Chemical Name: Acetic acid, (naphthalenyloxy)-
CAS Number: 2976-75-2
Product Number: AG002ZBP(AGN-PC-0JLPXW)
Synonyms:
MDL No:
Molecular Formula: C12H10O3
Molecular Weight: 202.2060

Identification/Properties

Properties
MP:
193-198 °C
BP:
388.7°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.5430 (estimate)
Computed Properties
Molecular Weight:
202.209g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
202.063g/mol
Monoisotopic Mass:
202.063g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
227
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:
H315-H319
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Naphthalen-1-yloxy)acetic acid, a versatile chemical compound, plays a crucial role in chemical synthesis as a key building block. This compound serves as an important precursor for the synthesis of various organic compounds due to its unique structural attributes. Its naphthalene ring provides aromatic properties that impart enhanced reactivity and selectivity in various chemical reactions. In organic synthesis, 2-(Naphthalen-1-yloxy)acetic acid can be utilized as a starting material for the preparation of advanced intermediates and complex molecules. Its functionality allows for the introduction of additional chemical groups, enabling the modification and fine-tuning of molecular structures to achieve specific properties or functionalities. Whether used in pharmaceutical synthesis, material science, or agrochemical development, this compound serves as a valuable tool in the hands of synthetic chemists seeking to create novel compounds with tailored properties and applications.