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M29959

Sigma-Aldrich

4-Methylbenzophenone

99%

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About This Item

Linear Formula:
CH3C6H4COC6H5
CAS Number:
134-84-9
Molecular Weight:
196.24
EC Number:
205-159-1
MDL number:
MFCD00008553
UNSPSC Code:
12162002
PubChem Substance ID:
24896789
NACRES:
NA.23

assay

99%

bp

326 °C (lit.)

mp

56.5-57 °C (lit.)

SMILES string

Cc1ccc(cc1)C(=O)c2ccccc2

InChI

1S/C14H12O/c1-11-7-9-13(10-8-11)14(15)12-5-3-2-4-6-12/h2-10H,1H3

InChI key

WXPWZZHELZEVPO-UHFFFAOYSA-N

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Related Categories

Application

  • Growth of 4-methylbenzophenone (4MB) single crystals by Czochralski method and its structural, mechanical and optical characterization: This study discusses the successful growth of 4-methylbenzophenone crystals and their properties, advancing materials science applications (Ramachandran et al., 2018).
  • Synthesis and characteristics of photopolymerized benzophenone: The synthesis of 4-methylbenzophenone acrylate for low migration applications in polymers was explored, suggesting its utility in safer material design (Tang et al., 2017).

pictograms

Health hazardEnvironment
GHS08,GHS09

signalword

Warning

hcodes

H373,H411

Hazard Classifications

Aquatic Chronic 2 - STOT RE 2 Oral

target_organs

Kidney,Liver

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
STBK5167
STBK4686
STBK2777
STBJ7687
STBJ4748

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Stanislav Gobec et al.
Bioorganic & medicinal chemistry letters, 15(23), 5170-5175 (2005-09-27)
Nonsteroidal anti-inflammatory drugs (NSAIDs) like indomethacin, flufenamic acid, and related compounds have been recently identified as potent inhibitors of AKR1C3. We report that some other NSAIDs (diclofenac and naproxen) also inhibit AKR1C3, with the IC(50) values in the low micromolar

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