1. Home
  2. Ethanone, 1-[1,1'-biphenyl]-4-yl-2-chloro-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Ethanone, 1-[1,1'-biphenyl]-4-yl-2-chloro-

ClCC(=O)c1ccc(cc1)c1ccccc1 Request for Quotation
Chemical Name: Ethanone, 1-[1,1'-biphenyl]-4-yl-2-chloro-
CAS Number: 635-84-7
Product Number: AG003LZF(AGN-PC-0JL91G)
Synonyms:
MDL No:
Molecular Formula: C14H11ClO
Molecular Weight: 230.6895

Identification/Properties

Properties
MP:
126°C
BP:
366.1°C at 760 mmHg
Storage:
Keep in dry area;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
230.691g/mol
XLogP3:
4.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
230.05g/mol
Monoisotopic Mass:
230.05g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
225
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:
H315-H319
Precautionary Statements:
P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


1-([1,1-Biphenyl]-4-yl)-2-chloroethanone, also known as $name$, is a versatile compound utilized in chemical synthesis for various applications. This compound acts as a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials. Its reactivity allows for the introduction of functional groups and modifications onto the biphenyl scaffold, enabling the creation of diverse chemical structures with tailored properties. In organic synthesis, $name$ serves as a key building block for the construction of complex molecules through various reactions such as nucleophilic substitution, Grignard reactions, and cross-coupling reactions. Its strategic placement of the chloroethanone moiety enables selective transformations and enables the incorporation of diverse molecular components, making it a valuable tool for synthetic chemists seeking to develop novel compounds with unique properties.