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Cyclohexene; compound with bromine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16489-73-9

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16489-73-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16489-73-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,8 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16489-73:
(7*1)+(6*6)+(5*4)+(4*8)+(3*9)+(2*7)+(1*3)=139
139 % 10 = 9
So 16489-73-9 is a valid CAS Registry Number.

16489-73-9Upstream product

16489-73-9Downstream Products

16489-73-9Relevant academic research and scientific papers

Direct Evidence for Bromine-Olefin Charge-Transfer Complexes as Essential Intermediates of the Fast Ionic Addition of Bromine to Cyclohexene

Bellucci, Giuseppe,Bianchini, Roberto,Ambrosetti, Roberto

, p. 2464 - 2471 (1985)

The addition of molecular bromine to cyclohexene in 1,2-dichloroethane has been investigated spectrophotometrically with the stopped-flow technique in the 15-35 deg C temperature range with and without cyclohexane added to the reaction medium.The third-or

Transition-State Barrier for Electrophilic Reactions. Solvation of Charge-Transfer Ion Pair as the Unifying Factor in Alkene Addition and Aromatic Substitution with Bromine

Fukuzumi, S.,Kochi, J. K.

, p. 7599 - 7609 (2007/10/02)

Alkenes and arenes are known to form 1:1 electron donor-acceptor complexes with molecular bromine.The disappearance of the charge-transfer (CT) absorption bands for these alkene and aromatic complexes coincides with the kinetics of electrophilic addition

Electrophilic Additions to Olefins. A New Approach to Unifying the Mechanisms of Bromination and Oxymercuration

Fukuzumi, S.,Kochi, J. K.

, p. 2783 - 2791 (2007/10/02)

Bromination and oxymercuration of carbon-carbon double bonds represent classical examples of electrophilic addition, but they nonetheless show quite divergent patterns of reactivities for various olefins.However, the olefin reactivities are identical when

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