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1-Bromo-2-methoxy-octane, also known as 2-methoxy-1-bromooctane, is an organic compound with the chemical formula C9H19BrO. It is a colorless liquid at room temperature and is derived from octane, an alkane with eight carbon atoms. The compound features a bromine atom attached to the first carbon atom and a methoxy group (-OCH3) attached to the second carbon atom. 1-Bromo-2-methoxy-octane is used as a chemical intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries. It is also employed as a solvent and a reagent in various chemical reactions. Due to its potential health and environmental hazards, it is essential to handle Octane, 1-bromo-2-methoxy- with proper safety measures and dispose of it according to regulations.

5935-18-2

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5935-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5935-18-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,3 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5935-18:
(6*5)+(5*9)+(4*3)+(3*5)+(2*1)+(1*8)=112
112 % 10 = 2
So 5935-18-2 is a valid CAS Registry Number.

5935-18-2Downstream Products

5935-18-2Relevant academic research and scientific papers

Comparative study of the vicinal functionalization of olefins with 2:1 bromide/bromate and iodide/iodate reagents

Agrawal, Manoj K.,Adimurthy, Subbarayappa,Ganguly, Bishwajit,Ghosh, Pushpito K.

, p. 2791 - 2797 (2009)

A comparative evaluation was made on the syntheses of vicinal halohydrins, halo methyl ethers, and halo acetates from olefins using 2:1 Br-/BrO3- and I-/IO3- reagents. In many cases both reagents afforded products selectively in high yields. The highest halogen atom efficiencies attained were 97% and 93% for Br-/BrO3- and I-/IO3-, respectively. Of the two reagents, I-/IO3- was established to be the preferred reagent for vicinal functionalization of linear alkenes and also for halo acetate preparation. However, only Br-/BrO3- was effective for vicinal functionalization of trans-stilbene and chalcones.

Micellar Effects upon Alkene Bromination. 2. The Role of Alkene Hydrophobicity

Cerichelli, Giorgio,Grande, Celeste,Luchetti, Luciana,Mancini, Giovanna

, p. 3025 - 3030 (2007/10/02)

Surface polarity of cettyltrimethylammonium bromide (CTAB) aqueous micelles was checked by use of as a probe the bromination reaction of a series of 1-alkenes and a water-soluble alkene, cis-4-cyclohexene-1,2-dicarboxylic acid dimethyl ester (I).There was

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