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1-Brommethyl-1-(2-bromethyl)-cyclohexan is a brominated cyclohexane derivative, featuring a cyclohexane ring with two bromine atoms attached to different carbon atoms. Specifically, one bromine atom is directly bonded to a methyl group (-CH3), while the other bromine atom is attached to the second carbon of the cyclohexane ring. This organic compound is characterized by its molecular formula C7H13Br2 and a molecular weight of 250.99 g/mol. It is a colorless liquid with a density of 1.54 g/cm3 and a boiling point of 243-245°C. Due to its reactive bromine atoms, 1-Brommethyl-1-(2-bromethyl)-cyclohexan can be used as an intermediate in the synthesis of various organic compounds, particularly those involving the formation of carbon-carbon bonds through radical reactions. It is also important to note that, like many brominated compounds, 1-brommethyl-1-(2-bromethyl)-cyclohexan may have potential environmental and health concerns due to its persistence and bioaccumulation properties.

3187-35-7

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3187-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3187-35-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,8 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3187-35:
(6*3)+(5*1)+(4*8)+(3*7)+(2*3)+(1*5)=87
87 % 10 = 7
So 3187-35-7 is a valid CAS Registry Number.

3187-35-7Downstream Products

3187-35-7Relevant academic research and scientific papers

Spiro[4,5] and spiro[4,6] carboxylic acids: Cyclic analogues of valproic acid. Synthesis and anticonvulsant evaluation

Scott,Moore,Zalucky,Nicholson,Lee,Hinko

, p. 413 - 417 (2007/10/02)

Spiro[4,5]decane-2-carboxylic acid, spiro[4,5]decane-2,2-dicarboxylic acid, spiro[4,6]undecane-2-carboxylic acid (12b), spiro[4,6]undecane-2,2-dicarboxylic acid, and spiro[4,6]undecane-2-acetic acid were synthesized by an improved method and evaluated for anticonvulsant activity. These analogues were synthesized to evaluate the role of the carboxylic acid group as an essential substituent in valproic acid (di-n-propylacetic acid, 1). Carbocyclic spiranes are known to resist metabolic alteration so that any activity elicited by these compounds would be due to the carboxylic acid function and not to any metabolic change. Spiro[4,6]undecane-2-carboxylic acid (12b) was the most active analogue tested and the pentylenetetrazol and picrotoxin evaluations of 12b compared favorably to 1. However, 12b failed to provide adequate protection against maximal electroshock seizures, bicuculline, or strychnine in mice. Possible reasons for these results are discussed.

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