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1-fluoro-3,4,5,6-tetrachloro-4-methoxycyclohexene is a complex organic compound with the molecular formula C7H5Cl4FO. It features a cyclohexene ring, which is a six-carbon ring with a double bond between two of the carbons. 1-fluoro-3,4,5,6-tetrachloro-4-methoxycyclohexene has four chlorine atoms attached to the ring at positions 3, 4, 5, and 6, a fluorine atom at position 1, and a methoxy group (-OCH3) at position 4. The presence of these halogen atoms and the methoxy group significantly alters the chemical properties and reactivity of the cyclohexene ring, making it a potentially useful intermediate in the synthesis of various pharmaceuticals and agrochemicals. Due to its complex structure and the presence of multiple functional groups, 1-fluoro-3,4,5,6-tetrachloro-4-methoxycyclohexene may exhibit unique chemical behaviors and require specific handling and storage conditions.

83801-97-2

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83801-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83801-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,8,0 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 83801-97:
(7*8)+(6*3)+(5*8)+(4*0)+(3*1)+(2*9)+(1*7)=142
142 % 10 = 2
So 83801-97-2 is a valid CAS Registry Number.

83801-97-2Upstream product

83801-97-2Downstream Products

83801-97-2Relevant academic research and scientific papers

Formation of Nonaromatic Products in the Chlorination of Simple Substituted Aromatic Ethers

Watson, William David

, p. 5270 - 5276 (2007/10/02)

The neat chlorination of 4-chloroanisole produces 1,3,4,5,6-pentachloro-4-methoxycyclohexene in 35percent yield.Mono- and dichlorinated anisoles and a variety of simple substituted anisoles were chlorinated to determine the generality of nonaromatic product formation. 3,4-Dichloroanisole, 4-fluoroanisole, 4-bromoanisole, 4-methylanisole, and 4-chlorophenetole form similar products based on their spectral properties.These products are proposed to form by a cis-1,2-chlorine addition followed by rapid cis-1,4 chlorine addition.On the basis of the NMR data, a predominate configuration is proposed.

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