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2-bromo-1-(2-bromoethoxy)-4-methoxybenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76429-64-6

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76429-64-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76429-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,2 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76429-64:
(7*7)+(6*6)+(5*4)+(4*2)+(3*9)+(2*6)+(1*4)=156
156 % 10 = 6
So 76429-64-6 is a valid CAS Registry Number.

76429-64-6Relevant academic research and scientific papers

HEMOGLOBIN MODIFIER COMPOUNDS AND USES THEREOF

-

, (2018/02/28)

Described herein are compounds, including pharmaceutically acceptable salts thereof, methods of making such compounds, pharmaceutical compositions comprising such compounds, and methods of using such compounds to treat, prevent or diagnose blood-based diseases, disorders or conditions.

INHIBITORS OF ACETYL-COA CARBOXYLASE

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Page/Page column 60-61, (2010/11/17)

The present invention relates to compounds that act as acetyl-CoA carboxylase (ACC) inhibitors. The invention also relates to methods of preparing the compounds, compositions containing the compounds, and to methods of treatment using the compounds.

Oxygen Heterocycles by the Parham Cyclialkylation

Bradsher, Charles K.,Reames, David C.

, p. 1384 - 1388 (2007/10/02)

The addition of butyllithium at -100 deg C to ω-bromoalkyl ethers of o-bromophenol (and its congeners) led to preferential exchange of the aryl bromine at position 2.The resulting organolithium reagents, under suitable conditions, cyclized to afford 2,3-dihydrobenzofurans (6), 3,4-dihydro-2H-1-benzopyrans (13), or 2,3,4,5-tetrahydro-1-benzoxepins (16) in good yields, but less satisfactory results were obtained with the intermediate expected to produce 8-methyl-3,4,5,6-tetrahydro-2H-1-benzoxocin (19). ω-Bromoethyl and ω-bromopropyl ethers of suitable dibromophenols were treated successively with 2 equiv of butyllithium and an electrophile to yield derivatives of 6 and 13.

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