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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)-

2-Naphthalenecarboxylic acid, 4,4'-methylenebis[3-hydroxy-, disodiumsalt

[O-]C(=O)c1cc2ccccc2c(c1O)Cc1c(O)c(cc2c1cccc2)C(=O)[O-].[Na+].[Na+] Request for Quotation
Chemical Name: 2-Naphthalenecarboxylic acid, 4,4'-methylenebis[3-hydroxy-, disodiumsalt
CAS Number: 6640-22-8
Product Number: AG003TJT(AGN-PC-0TKOAF)
Synonyms:
MDL No:
Molecular Formula: C23H14Na2O6
Molecular Weight: 432.3332

Identification/Properties

Properties
MP:
300 °C
Storage:
Room Temperature;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
432.339g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
4
Exact Mass:
432.059g/mol
Monoisotopic Mass:
432.059g/mol
Topological Polar Surface Area:
121A^2
Heavy Atom Count:
31
Formal Charge:
0
Complexity:
569
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:
3
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Sodium 4,4'-methylenebis(3-hydroxy-2-naphthoate) is a versatile compound widely utilized in chemical synthesis. This compound acts as a key building block in the production of various organic materials and pharmaceuticals due to its unique chemical properties.In chemical synthesis, Sodium 4,4'-methylenebis(3-hydroxy-2-naphthoate) serves as a crucial intermediate for creating complex molecules. It can be employed as a crosslinking agent in polymer chemistry, contributing to the formation of strong and durable polymeric materials. Additionally, this compound can be used as a coupling reagent to facilitate the bonding of different functional groups in organic reactions, enabling the synthesis of intricate organic compounds.Furthermore, Sodium 4,4'-methylenebis(3-hydroxy-2-naphthoate) finds applications in the pharmaceutical industry for the development of drug molecules. Its ability to participate in various chemical reactions and form stable structures makes it a valuable component in the synthesis of pharmaceutical intermediates and active compounds.Overall, Sodium 4,4'-methylenebis(3-hydroxy-2-naphthoate) plays a crucial role in chemical synthesis by enabling the construction of diverse organic molecules with performance-boosting properties in industries such as polymers, pharmaceuticals, and materials science.