Product Name:Methyl 5-bromo-2-methylbenzoate

IUPAC Name:methyl 5-bromo-2-methylbenzoate

CAS:79669-50-4
Molecular Formula:C9H9BrO2
Purity:95%
Catalog Number:CM160642
Molecular Weight:229.07

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CM160642-100g in stock dždž

For R&D use only.

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Product Details

CAS NO:79669-50-4
Molecular Formula:C9H9BrO2
Melting Point:-
Smiles Code:C1=C(C(=CC=C1Br)C)C(=O)OC
Density:
Catalog Number:CM160642
Molecular Weight:229.07
Boiling Point:258.9°C at 760 mmHg
MDL No:MFCD09839555
Storage:Keep in a tight container and store at ambient temperature

Category Infos

Benzenes
Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.

Column Infos

MRT-2359
Aberrant MYC pathway activation is found in cancer cells, while MYC-induced protein translation depends on GSPT1. Molecular glues targeting GSPT1 is identified as a potential treatment method in oncology. Monte Rosa’s MRT-2359 is an oral and selective molecular glue degrader of the translation termination factor GSPT1. The targeted GSPT1 degradation results in disrupting MYC-driven protein translation and reducing MYC-oncogenic signaling.
MRT-2359 is in an ongoing phase 1/2 study in MYC-driven solid tumors with a current assessment of 0.75 mg dose level. The final phase 2 dose determination and updated clinical results are anticipated in the second half of 2024. MRT-2359 previously received Fast Track Designation in patients with previously treated, metastatic NSCLC with L-MYC or N-MYC expression, Orphan Drug Designation in small cell lung cancer (SCLC), and Fast Track Designation in previously treated, metastatic SCLC with L-MYC or N-MYC expression.

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