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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)-

3-hydroxynaphthalene-1-carbaldehyde

O=Cc1cc(O)cc2c1cccc2 Request for Quotation
Chemical Name: 3-hydroxynaphthalene-1-carbaldehyde
CAS Number: 91136-43-5
Product Number: AG003JJ6(AGN-PC-00LKAI)
Synonyms:
MDL No: MFCD17012437
Molecular Formula: C11H8O2
Molecular Weight: 172.1800

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
172.183g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
172.052g/mol
Monoisotopic Mass:
172.052g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
191
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:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Hydroxy-1-naphthaldehyde is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. One of its key applications is as a building block for the synthesis of various organic compounds. In organic chemistry, this compound is commonly used as a precursor for the preparation of complex molecules and pharmaceutical intermediates.Due to its ability to undergo various chemical transformations, 3-Hydroxy-1-naphthaldehyde serves as a valuable starting material in the synthesis of heterocyclic compounds, particularly in the production of pharmaceutical drugs and agrochemicals. Its hydroxy and aldehyde functional groups make it a suitable candidate for different reactions such as condensation, nucleophilic addition, and oxidation, allowing for the creation of a wide range of substituted derivatives.Furthermore, 3-Hydroxy-1-naphthaldehyde is employed in the development of fluorescent dyes and optical brighteners used in the textile industry. Its aromatic structure and functional groups make it ideal for the modification of organic molecules to impart desired optical properties.Overall, the application of 3-Hydroxy-1-naphthaldehyde in chemical synthesis extends to various industries, including pharmaceuticals, agrochemicals, and materials science, where its reactivity and versatility play a crucial role in the creation of novel compounds and functional materials.