CAS 16331-45-6: 4-Ethylbenzoyl chloride
Formula:C9H9ClO
InChI:InChI=1S/C9H9ClO/c1-2-7-3-5-8(6-4-7)9(10)11/h3-6H,2H2,1H3
InChI key:InChIKey=AVTLLLZVYYPGFX-UHFFFAOYSA-N
SMILES:C(Cl)(=O)C1=CC=C(CC)C=C1
Synonyms:- 4-Ethylbenzene-1-Carbonyl Chloride
- 4-Ethylbenzoyl choride
- Benzoyl Chloride, 4-Ethyl-
- Benzoyl chloride, p-ethyl-
- Ethylbenzoyl Chloride
- P-Ethylbenzoyl Chloride
- Pebc
- PenicillinGProcaineSterileBp98
- Timtec-Bb Sbb006540
- 4-Ethylbenzoyl chloride
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Found 6 products.
4-Ethylbenzoyl chloride, 98+%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C9H9ClOPurity:98+%Color and Shape:Clear colorless to yellow, LiquidMolecular weight:168.624-Ethylbenzoyl chloride, 97%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C9H9ClOPurity:97%Color and Shape:Liquid, Clear colorless to yellowMolecular weight:168.62Benzoyl chloride, 4-ethyl-
CAS:Formula:C9H9ClOPurity:98%Color and Shape:LiquidMolecular weight:168.62024-Ethylbenzene-1-carbonyl chloride
CAS:4-Ethylbenzene-1-carbonyl chloridePurity:98%Color and Shape:Colourless - Yellow LiquidMolecular weight:168.62g/mol4-Ethylbenzoyl chloride
CAS:4-Ethylbenzoyl chloride is a compound that inhibits the growth of cells. It has been used as an analytical reagent in clinical chemistry and as a research tool for cancer studies. 4-Ethylbenzoyl chloride has been shown to inhibit the growth of mammalian cells, including human colon carcinoma HCT116 cells, by inhibiting protein synthesis through inhibition of DNA transcription and translation. The mechanism of action is related to its ability to act as a membrane-permeable chloride ion channel and nitrate reductase inhibitor. This compound also reacts with supercritical carbon dioxide, forming benzoate and benzamidine.Formula:C2H5C6H4COClPurity:Min. 95%Molecular weight:168.62 g/mol
