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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)-

Benzenemethanol, 3-hydroxy-

OCc1cccc(c1)O Request for Quotation
Chemical Name: Benzenemethanol, 3-hydroxy-
CAS Number: 620-24-6
Product Number: AG003JKB(AGN-PC-0CV47Q)
Synonyms:
MDL No:
Molecular Formula: C7H8O2
Molecular Weight: 124.1372

Identification/Properties

Properties
MP:
69-72 °C(lit.)
BP:
289.2°C at 760 mmHg
Storage:
Room Temperature;Inert atmosphere;
Form:
Solid
Refractive Index:
1.5035 (estimate)
Computed Properties
Molecular Weight:
124.139g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
124.052g/mol
Monoisotopic Mass:
124.052g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
83
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(Hydroxymethyl)phenol, or commonly known as resorcinol monomethyl ether, is a versatile compound widely utilized in various chemical synthesis processes. This compound serves as a crucial intermediate in the production of pharmaceuticals, agrochemicals, fragrances, and dyes. Its hydroxyl and methoxy groups allow for a range of functionalization reactions, making it a valuable building block in organic synthesis. In the pharmaceutical industry, 3-(Hydroxymethyl)phenol is employed in the synthesis of antiseptics, antihistamines, and anticancer agents. Additionally, it is used in the formulation of hair dyes, perfumes, and other cosmetic products. The compound's reactivity and compatibility with different reaction conditions make it a favorable choice for chemists seeking to introduce functional groups or create complex molecular structures.