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Key Documents

194387

Sigma-Aldrich

2-Chlorobenzophenone

≥99%

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About This Item

Linear Formula:
ClC6H4COC6H5
CAS Number:
Molecular Weight:
216.66
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

≥99%

bp

330 °C (lit.)

mp

44-47 °C (lit.)

SMILES string

Clc1ccccc1C(=O)c2ccccc2

InChI

1S/C13H9ClO/c14-12-9-5-4-8-11(12)13(15)10-6-2-1-3-7-10/h1-9H

InChI key

VMHYWKBKHMYRNF-UHFFFAOYSA-N

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General description

Thermodynamics of formation of inclusion complex between 2-chlorobenzophenone and cyclomaltoheptaose (β-cyclodextrin) has been investigated by UV-vis spectroscopy and reversed-phase liquid chromatography. 2-Chlorobenzophenone undergoes reduction in the presence of LiAlH4 and (R)-(-)-2-(2-iso-indolinyl)butan-1-ol to afford the corresponding benzhydrols.

Application

2-Chlorobenzophenone was used in the synthesis of 1-(2-chlorophenyl)isoquinolin-3-yl trifluoromethanesulfonate.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Customers Also Viewed

Matias I Sancho et al.
Carbohydrate research, 346(13), 1978-1984 (2011-06-07)
A thermodynamic study of the inclusion process between 2-chlorobenzophenone (2ClBP) and cyclomaltoheptaose (β-cyclodextrin, β-CD) was performed using UV-vis spectroscopy, reversed-phase liquid chromatography (RP-HPLC), and molecular modeling (PM6). Spectrophotometric measurements in aqueous solutions were performed at different temperatures. The stoichiometry of
Synthesis of N-methyl-N-(1-methylpropyl)-1-(2-chlorophenyl) isoquinoline-3-[11 C] carboxamide ([11 C-carbonyl] PK11195) and some analogues using [11 C] carbon monoxide and 1-(2-chlorophenyl) isoquinolin-3-yl triflate.
Rahman O, et al.
Journal of the Chemical Society. Perkin Transactions 1, 23, 2699-2703 (2002)
Asymmetric reductions of ketones using lithium aluminium hydride modified with N, N-dialkyl derivatives of (R)-(-)-2-aminobutan-1-ol.
Brown E, et al.
Tetrahedron Asymmetry, 2(5), 339-342 (1991)

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