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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)-

1,8-Naphthalenedimethanol

OCc1cccc2c1c(CO)ccc2 Request for Quotation
Chemical Name: 1,8-Naphthalenedimethanol
CAS Number: 2026-08-6
Product Number: AG0028BW(AGN-PC-0JLBVV)
Synonyms:
MDL No:
Molecular Formula: C12H12O2
Molecular Weight: 188.2225

Identification/Properties

Properties
MP:
153-156 °C(lit.)
BP:
411.1°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
188.226g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
188.084g/mol
Monoisotopic Mass:
188.084g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
163
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:
H315-H319
Precautionary Statements:
P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Naphthalene-1,8-diyldimethanol, also known as 1,8-bis(hydroxymethyl)naphthalene, is a versatile compound widely used in chemical synthesis processes. This compound serves as a key building block in the creation of various polymers, resins, and pharmaceutical compounds. Its unique chemical structure allows for the formation of strong covalent bonds with other molecules, making it a valuable tool in the development of advanced materials.In chemical synthesis, Naphthalene-1,8-diyldimethanol plays a crucial role as a crosslinking agent in the production of polyesters and polyurethanes. By reacting with diisocyanates or dicarboxylic acids, this compound contributes to the formation of three-dimensional network structures, enhancing the mechanical strength and thermal stability of the final polymer products. Additionally, the hydroxyl groups in Naphthalene-1,8-diyldimethanol can undergo further functionalization reactions, allowing for the fine-tuning of polymer properties such as flexibility, adhesion, and chemical resistance.Furthermore, Naphthalene-1,8-diyldimethanol is utilized in the synthesis of various pharmaceutical intermediates due to its biocompatibility and pharmacological properties. Its presence in drug molecules can enhance their solubility, bioavailability, and therapeutic effects. The ability of Naphthalene-1,8-diyldimethanol to form stable complexes with active pharmaceutical ingredients makes it a valuable component in drug delivery systems and controlled release formulations.Overall, the application of Naphthalene-1,8-diyldimethanol in chemical synthesis enables the production of diverse materials with tailored properties and functionality, making it a vital ingredient in the development of advanced polymers, resins, and pharmaceutical compounds.