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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)-

1H-Inden-4-ol, 2,3-dihydro-

Oc1cccc2c1CCC2 Request for Quotation
Chemical Name: 1H-Inden-4-ol, 2,3-dihydro-
CAS Number: 1641-41-4
Product Number: AG001UNT(AGN-PC-0JLBHE)
Synonyms:
MDL No:
Molecular Formula: C9H10O
Molecular Weight: 134.1751

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
134.178g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
134.073g/mol
Monoisotopic Mass:
134.073g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
122
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Indanol, also known as 4-hydroxyindole, is a versatile compound widely used in chemical synthesis for various applications. In particular, 4-Indanol serves as an essential building block in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it a valuable intermediate in the synthesis of complex organic molecules. Additionally, 4-Indanol is employed as a key starting material in the preparation of indole derivatives, which have diverse biological activities and are crucial in medicinal chemistry research. Through strategic transformations, 4-Indanol can be utilized to introduce functional groups and modify molecular properties, enabling the creation of novel compounds with enhanced properties and desired functionalities. Its applications in chemical synthesis are pivotal for the development of new materials and compounds with potential applications in various industries.