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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)-

5-(2-chloroethyl)-2,3-dihydro-1-benzofuran

ClCCc1ccc2c(c1)CCO2 Request for Quotation
Chemical Name: 5-(2-chloroethyl)-2,3-dihydro-1-benzofuran
CAS Number: 943034-50-2
Product Number: AG005Z7W(AGN-PC-04USLL)
Synonyms:
MDL No:
Molecular Formula: C10H11ClO
Molecular Weight: 182.6467

Identification/Properties

Properties
BP:
284.4 °C at 760 mmHg
Computed Properties
Molecular Weight:
182.647g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
182.05g/mol
Monoisotopic Mass:
182.05g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
149
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:
N/A
Signal Word:
UN#:
N/A
Hazard Statements:
-
Precautionary Statements:
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The chemical compound 5-(2-Chloroethyl)-2,3-dihydrobenzofuran plays a crucial role in chemical synthesis as a versatile building block with diverse applications. Its unique structure and reactivity make it a valuable intermediate in the production of various organic compounds. In chemical synthesis, it is commonly used as a reagent in the preparation of pharmaceuticals, agrochemicals, and fine chemicals due to its ability to participate in various reactions such as nucleophilic substitution, electrophilic aromatic substitution, and radical reactions. Additionally, its incorporation into complex molecules allows for the creation of novel structures with potential biological activities. This compound's versatility and synthetic utility make it a valuable tool for the development of new chemical entities and the advancement of organic synthesis.