cas 90347-66-3|| where to buy methyl 3-iodo-4-methylbenzoate

Product Name:methyl 3-iodo-4-methylbenzoate

IUPAC Name:methyl 3-iodo-4-methylbenzoate

Packing Unit	Available Stock	Price($)
CM101804-100g	in stock	ǟǎ
CM101804-500g	in stock	ţǟţ

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: CAS NO:90347-66-3; Molecular Formula:C9H9IO2; Melting Point:-; Smiles Code:O=C(OC)C1=CC=C(C)C(I)=C1; Density:1.666g/cm3

: Catalog Number:CM101804; Molecular Weight:276.07; Boiling Point:302.9°C at 760 mmHg; MDL No:MFCD00230583; Storage:Store at 2-8°C.

: 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.

: Carbonyl Compounds; In organic chemistry, a carbonyl group is a functional group with the formula C=O, composed of a carbon atom double-bonded to an oxygen atom, and it is divalent at the C atom. It is common to several classes of organic compounds (such as aldehydes, ketones and carboxylic acids), as part of many larger functional groups. A compound containing a carbonyl group is often referred to as a carbonyl compound.

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Olverembatinib (HQP1351) is an oral, third-generation BCR-ABL1 tyrosine kinase inhibitor (TKI) developed by Ascentage Pharma for the treatment of chronic myeloid leukaemia (CML), acute myeloid leukaemia, acute lymphoblastic leukaemia (ALL) and solid tumours, including gastrointestinal stromal tumours (GIST). Olverembatinib is an ATP binding-site inhibitor of wild type BCR-ABL1 kinase and a broad spectrum of BCR-ABL1 mutants, including mutant T315I, which confers resistance against all first- and second-generation TKIs.