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Key Documents

M29959

Sigma-Aldrich

4-Methylbenzophenone

99%

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About This Item

Linear Formula:
CH3C6H4COC6H5
CAS Number:
Molecular Weight:
196.24
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
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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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

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Chronic 2 - STOT RE 2 Oral

Target Organs

Kidney,Liver

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)

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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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