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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-Benzofuranmethanol, 2,3-dihydro-

OCC1Cc2c(O1)cccc2 Request for Quotation
Chemical Name: 2-Benzofuranmethanol, 2,3-dihydro-
CAS Number: 66158-96-1
Product Number: AG00FB9C(AGN-PC-0C2GCB)
Synonyms:
MDL No:
Molecular Formula: C9H10O2
Molecular Weight: 150.1745

Identification/Properties

Computed Properties
Molecular Weight:
150.177g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
150.068g/mol
Monoisotopic Mass:
150.068g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
136
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Utilizing (2,3-Dihydrobenzofuran-2-yl)methanol in chemical synthesis offers a versatile and valuable tool in the production of various compounds. As a key building block, this compound plays a crucial role in the creation of complex molecules through efficient and selective transformations. Its structural features provide unique opportunities for the construction of heterocyclic frameworks and functionalized organic molecules. In organic synthesis, (2,3-Dihydrobenzofuran-2-yl)methanol serves as a strategic intermediate for the introduction of diverse functional groups, enabling the synthesis of biologically active compounds, pharmaceuticals, and advanced materials. Its synthetic versatility and reactivity open up pathways for the development of novel chemical entities and the exploration of new reaction mechanisms, making it a valuable component in the toolbox of synthetic chemists.