1. Home
  2. 4-​Hydroxy-​naphthalene-​2-​carboxylic acid methyｌ ester

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

4-​Hydroxy-​naphthalene-​2-​carboxylic acid methyｌ ester

COC(=O)c1cc(O)c2c(c1)cccc2 Request for Quotation
Chemical Name: 4-​Hydroxy-​naphthalene-​2-​carboxylic acid methyｌ ester
CAS Number: 34205-71-5
Product Number: AG00C6D5(AGN-PC-0WALMZ)
Synonyms:
MDL No:
Molecular Formula: C12H10O3
Molecular Weight: 202.2060

Identification/Properties

Computed Properties
Molecular Weight:
202.209g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
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:
239
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:
N/A
Signal Word:
UN#:
N/A
Hazard Statements:
-
Precautionary Statements:
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Methyl 4-hydroxy-2-naphthoate, also known as Methyl 4-hydroxy-2-naphthoate, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and fragrances. Its unique chemical structure makes it a valuable precursor for the synthesis of complex organic molecules. By undergoing various chemical reactions, Methyl 4-hydroxy-2-naphthoate can be transformed into a wide array of functionalized compounds with diverse properties and applications. Its presence in chemical synthesis processes contributes to the development of innovative materials and compounds that have significant implications in the fields of medicine, agriculture, and perfumery.