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methyl 5-bromo-2-(dibromomethyl)-benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1265286-99-4

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1265286-99-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1265286-99-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,5,2,8 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1265286-99:
(9*1)+(8*2)+(7*6)+(6*5)+(5*2)+(4*8)+(3*6)+(2*9)+(1*9)=184
184 % 10 = 4
So 1265286-99-4 is a valid CAS Registry Number.

1265286-99-4Relevant academic research and scientific papers

Preparation method and application of water-soluble supramolecular organic cage compound for detecting pyridine salt substances in water

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, (2021/10/27)

The preparation method comprises the following steps: synthesizing compound S1, wherein compound S1 is 5 -bromo -2 - methylbenzoate. Compound S2 in which compound S2 is 5 - bromo -2 - (dibromomethyl) benzoate. The method has the beneficial effects that qu

COMPOUNDS AND USES THEREOF

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, (2021/08/06)

The present disclosure features compounds useful for the treatment of BAF complex-related disorders.

COMPOUNDS AND USES THEREOF

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Page/Page column 71, (2021/08/06)

The present disclosure features compounds useful for the treatment of BAF complex-related disorders.

BRIDGED BICYCLIC COMPOUNDS AS FARNESOID X RECEPTOR MODULATORS

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Paragraph 1564-1565, (2019/05/15)

The present invention provides compounds of Formula (I): or stereoisomers, tautomers, or pharmaceutically acceptable salts or solvates thereof, wherein all the variables are as defined herein. These compounds modulate the activity of farnesoid X receptor

Synthesis and characterization of π-extended porphyrins as potential precursors for the formation of columnar mesophases: Design principles for columnar mesophases need revision?

Herzog, Beat,Neier, Reinhard

experimental part, p. 29 - 44 (2011/06/18)

A series of meso-a bridged extended porphyrins substituted with long aliphatic chains were synthesized and fully characterized. Two different synthetic strategies were tested to obtain the target structures. The synthetic steps were optimized in order to obtain scalable routes for the production of sufficient quantities of η-extended porphyrins for material science studies. The porphyrins were obtained either as free bases or complexed with Ni II or CuII. UV-Vis spectroscopy and polarized light microscopy was used for the analysis of the material properties of the η-extended porphyrins. The results obtained with our compounds are not compatible with the results reported in the literature. ARKAT-USA, Inc.

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