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1-(bromomethyl)-2-chloro-3,5-dimethoxybenzene is an organic compound with the molecular formula C9H10BrClO2. It is a colorless to pale yellow liquid with a molecular weight of 273.53 g/mol. 1-(bromomethyl)-2-chloro-3,5-dimethoxybenzene is characterized by the presence of a benzene ring, with a bromine atom attached to the methyl group at the 1-position, a chlorine atom at the 2-position, and two methoxy groups at the 3 and 5 positions. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its versatile functional groups, which can be further modified to introduce different chemical properties. The compound is sensitive to heat and light, and it is typically stored under cool, dry conditions to maintain its stability.

5859-85-8

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5859-85-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5859-85-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,5 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5859-85:
(6*5)+(5*8)+(4*5)+(3*9)+(2*8)+(1*5)=138
138 % 10 = 8
So 5859-85-8 is a valid CAS Registry Number.

5859-85-8Relevant academic research and scientific papers

FGFR INHIBITOR AND APPLICATION THEREOF

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, (2020/01/22)

An azatricyclic compound (as represented by formula I) which acts as an inhibitor of fibroblast growth factor receptors (FGFR), as well as a pharmaceutical composition thereof, a preparation method, and a use therefor in the treatment of FGFR-mediated diseases. The azatricyclic compound exerts an effect by means of participating in the regulation of a plurality of processes such as cell proliferation, apoptosis, migration, neovascularization, and the like. AA%%%Formula (I).

Diastereoselective synthesis of complex cis-hexahydroindanes by reductive alkylation

Kaplan, Hilan Z.,Rendina, Victor L.,Kingsbury, Jason S.

, p. 4620 - 4626 (2013/06/27)

An efficient and operationally simple approach to complex cis-hexahydroindanes is reported. Upon Birch reduction of unprotected, C4-alkylated tetrahydroindanols and electrophilic trapping of the tetrasubstituted enolate, cis-fused products are formed with a new stereogenic quaternary carbon. The reaction is convergent, completely diastereoselective, and shows a broad scope with regard to the electrophile.

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