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397210

Sigma-Aldrich

2-Amino-5-chloro-2′-fluorobenzophenone

98%

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About This Item

Linear Formula:
H2NC6H3(Cl)C(O)C6H4F
CAS Number:
784-38-3
Molecular Weight:
249.67
EC Number:
212-316-8
MDL number:
MFCD00038381
UNSPSC Code:
12352100
PubChem Substance ID:
24864693
NACRES:
NA.22

Assay

98%

mp

95-98 °C (lit.)

SMILES string

Nc1ccc(Cl)cc1C(=O)c2ccccc2F

InChI

1S/C13H9ClFNO/c14-8-5-6-12(16)10(7-8)13(17)9-3-1-2-4-11(9)15/h1-7H,16H2

InChI key

GTGMXPIQRQSORU-UHFFFAOYSA-N

Related Categories

Application

2-Amino-5-chloro-2′-fluorobenzophenone is suitable electrophilic coupling reagent for the determination of iron(III) in environmental waters, soils and industrial effluent samples. It may be used in the synthesis of following:
  • 2,4-disubstituted quinolones, via Meyer-Schuster rearrangement
  • 6-chloro-2-methyl-4-(2-fluorophenyl) quinazoline
  • N-desalkylflurazepam
  • benzotriazepines
  • diazepam-related benzodiazepines.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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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Ionic liquid-an efficient recycalable system for the synthesis of 2, 4-disubstituted quinolines via Meyer-Schuster rearrangement.
Saqrma R and Prajapati D.
Synlett, 19, 3001-3005 (2008)
Bhawana Sati et al.
Acta pharmaceutica (Zagreb, Croatia), 63(3), 385-396 (2013-10-25)
During the manufacture of bulk drug midazolam various impurities arised that can be the related products or degradation products. Structures of eight impurities that can arise during the manufacture of bulk drug midazolam were proposed. In the present work, synthesis
J. Chem. Res. Synop., 2-2 (1991)
Journal of the American Chemical Society, 112, 3969-3969 (1990)

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