2-(4-Chlorophenyl)acetophenone - CAS 6332-83-8
Catalog: |
BB032099 |
Product Name: |
2-(4-Chlorophenyl)acetophenone |
CAS: |
6332-83-8 |
Synonyms: |
2-(4-chlorophenyl)-1-phenylethanone; 2-(4-chlorophenyl)-1-phenylethanone |
IUPAC Name: | 2-(4-chlorophenyl)-1-phenylethanone |
Description: | 2-(4-Chlorophenyl)acetophenone (CAS# 6332-83-8) is an intermediate in the synthesis of pyrrobutamine which is antihistaminic. Also used as a reagent on the synthesis of 2,3-diaryl-6,7-dihydro-5H-1,4-diazepines which display antileukemic annd antiplatelet properties. |
Molecular Weight: | 230.69 |
Molecular Formula: | C14H11ClO |
Canonical SMILES: | C1=CC=C(C=C1)C(=O)CC2=CC=C(C=C2)Cl |
InChI: | InChI=1S/C14H11ClO/c15-13-8-6-11(7-9-13)10-14(16)12-4-2-1-3-5-12/h1-9H,10H2 |
InChI Key: | HGIDMJOUQKOWMX-UHFFFAOYSA-N |
Density: | 1.587 g/cm3 |
MDL: | MFCD02260686 |
LogP: | 3.76540 |
Publication Number | Title | Priority Date |
CN-111269227-A | Process for preparing 1,2, 3-trisubstituted indolizine derivatives | 20200228 |
WO-2020204733-A1 | A solvent drying composition and processes therfor | 20190403 |
AU-2018346086-A1 | A salt recovery solution and processes of use thereof | 20171003 |
CA-3075922-A1 | A salt recovery solution and processes of use thereof | 20171003 |
CN-111225875-A | Salt recovery solution and method of using salt recovery solution | 20171003 |
Complexity: | 225 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 230.0498427 |
Formal Charge: | 0 |
Heavy Atom Count: | 16 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 230.0498427 |
Rotatable Bond Count: | 3 |
Topological Polar Surface Area: | 17.1 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 3.8 |
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