Product Name:6-Amino-3-bromo-2-methylbenzoic acid

IUPAC Name:6-amino-3-bromo-2-methylbenzoic acid

CAS:124341-06-6
Molecular Formula:C8H8BrNO2
Purity:95%
Catalog Number:CM248452
Molecular Weight:230.06

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CM248452-250mg in stock ũȺ
CM248452-1g in stock ƛǜŵ
CM248452-5g in stock ŵȺũ

For R&D use only.

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Product Details

CAS NO:124341-06-6
Molecular Formula:C8H8BrNO2
Melting Point:-
Smiles Code:O=C(O)C1=C(N)C=CC(Br)=C1C
Density:
Catalog Number:CM248452
Molecular Weight:230.06
Boiling Point:346.4±42.0°C at 760 mmHg
MDL No:
Storage:Store at 2-8°C.

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.

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Tinlorafenib
The Journal of Medicinal Chemistry releases an article titled "Identification of the Clinical Candidate PF-07284890 (ARRY-461), a Highly Potent and Brain Penetrant BRAF Inhibitor for the Treatment of Cancer". Mutations in the BRAF gene result in MAPK pathway activation that are most commonly found in human melanomas. The BRAF V600E mutation is among the most frequent types. Present BRAF inhibitors have significantly improved treatment outcomes for patients with BRAF V600-mutant cancers. However, their effectiveness is limited by disease progression in the brain as they don’t adequately penetrate the blood-brain barrier (BBB).
Pfizer’s Tinlorafenib (formerly PF 07284890) is a highly brain-penetrant inhibitor of BRAF V600-mutant tumors, and currently in a phase 1 clinical trial (NCT04543188). 

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