Product Name:2-(o-Tolylcarbamoyl)naphthalen-3-yl 2-chloroacetate

IUPAC Name:3-[(2-methylphenyl)carbamoyl]naphthalen-2-yl 2-chloroacetate

CAS:35245-26-2
Molecular Formula:C20H16ClNO3
Purity:95%
Catalog Number:CM140198
Molecular Weight:353.8

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CM140198-5g 3-4 Weeks ưȀȀ

For R&D use only.

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Product Details

CAS NO:35245-26-2
Molecular Formula:C20H16ClNO3
Melting Point:-
Smiles Code:O=C(OC1=C(C(NC2=CC=CC=C2C)=O)C=C3C=CC=CC3=C1)CCl
Density:
Catalog Number:CM140198
Molecular Weight:353.8
Boiling Point:460.3°C at 760 mmHg
MDL No:MFCD00042714
Storage:Store at 2-8°C.

Category Infos

Naphthalenes
Naphthalene is a hydrocarbon produced by the distillation of coal tar and is an aromatic white crystalline substance. Naphthalene is the most abundant component in coal tar. It is used as an insect repellant and insect fumigant. The compound is used in the manufacture of celluloid, dyes, hydrogenated naphthalenes, oil fumes, smokeless powders and synthetic resins.

Column Infos



Product Other Information

Product Overview 2-(O-tolylcarbamoyl)naphthalen-3-yl 2-chloroacetate, also known as OTCN-3-Cl, is a novel small-molecule inhibitor of the enzyme phosphoinositide 3-kinase (PI3K).
Synthesis Method 2-(O-tolylcarbamoyl)naphthalen-3-yl 2-chloroacetate is synthesized by the reaction of 2-chloroacetyl chloride with o-tolylcarbamoyl naphthalene-3-carboxylic acid. The reaction is carried out in an inert atmosphere and requires a catalyst, such as pyridine, to drive the reaction. 
Chemical Properties 2-(O-tolylcarbamoyl)naphthalen-3-yl 2-chloroacetate is relatively easy to synthesize and purify, making it a suitable choice for laboratory experiments.
Synthesis and Application 2-(O-tolylcarbamoyl)naphthalen-3-yl 2-chloroacetate has been used in a variety of scientific research applications, including the study of PI3K-mediated signaling pathways in cancer cells and other cell types. 2-(O-tolylcarbamoyl)naphthalen-3-yl 2-chloroacetate has also been used to investigate the effects of PI3K inhibition on cell proliferation, migration, and invasion in vitro. Additionally, 2-(O-tolylcarbamoyl)naphthalen-3-yl 2-chloroacetate has been used to investigate the effects of PI3K inhibition on tumor growth and metastasis in vivo.
Future Directions Further studies may investigate the effects of 2-(O-tolylcarbamoyl)naphthalen-3-yl 2-chloroacetate on other cellular processes, such as apoptosis, autophagy, and angiogenesis. Additionally, further research may investigate the effects of 2-(O-tolylcarbamoyl)naphthalen-3-yl 2-chloroacetate on other signaling pathways, such as the Wnt/β-catenin pathway, and its potential use in other therapeutic applications. Finally, further studies may investigate the mechanisms of resistance to 2-(O-tolylcarbamoyl)naphthalen-3-yl 2-chloroacetate in cancer cells, which may lead to the development of novel strategies for overcoming drug resistance.