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BROMADOL HCL BDPC

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    Bromadol HCL
    Bromadol HCL BDPC
    Cyclohexanol, 4-(4-broMophenyl)-4-(diMethylaMino)-1-(2-phenylethyl)-, trans-
    Bromadol HCl4-(4-bromophenyl)-4-(dimethylamino)-1-phenethylcyclohexanol hydrochloride
    BDPC
    bromadol
    Bromadol CAS NO.77239-98-6
    Bromadol hight quality CAS NO.77239-98-6
    Bromadol HCL (BDPC) white powder CAS NO.77239-98-6
    Reaxys ID: 2819173
    77239-98-6
    pharmaceutical intermediate
BDPC;bromadol;Bromadol HCL;Bromadol HCL BDPC;Reaxys ID: 2819173;Bromadol CAS NO.77239-98-6;Bromadol hight quality CAS NO.77239-98-6;Bromadol HCL (BDPC) white powder CAS NO.77239-98-6;Cyclohexanol, 4-(4-broMophenyl)-4-(diMethylaMino)-1-(2-phenylethyl)-, trans-;Bromadol HCl4-(4-bromophenyl)-4-(dimethylamino)-1-phenethylcyclohexanol hydrochloride
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Description

Bromadol HCL (BDPC) (efficient name 4-(4-bromophenyl)- 4-(dimethylamino)– 1-(2-phenylethyl)cyclohexanol; otherwise called bromadol) is a strong opiate pain relieving with an unmistakable arylcyclohexylamine substance structure. It was created by Daniel Lednicer at Upjohn in the 1970s.[1] Initial studies assessed that it was around 10,000 times the quality of morphine in creature models.[2] However, later studies doled out an estimation of 504 times the strength of morphine for the more dynamic trans-isomer.[3] To date, it is obscure if this medication has been utilized by people, nonetheless, it was seized alongside three kilograms of acetylfentanyl in an April 25, 2013 police activity in Montreal, Canada. Notwithstanding taking precautionary measures, no less than two officers got to be inebriated because of taking care of the drugs.

Bromadol HCL BDPC has never been utilized as a part of people, however would be required to create impacts like those of other strong opioid agonists, including solid absense of pain, sedation, happiness, stoppage, tingling and respiratory sadness which could be unsafe or lethal. BDPC Formula :C22H29BrClNO Resistance and reliance would be required to grow quickly in light of the intensity

of the medication, as it is of a comparative quality to sufentanil thus would in all likelihood cause affirmed tachyphylaxis

taking after rehashed dosing, as is seen with the powerful fentanyl analogs.

Structure-movement connections

Bromadol HCL BDPC (systematic name 4-(4-bromophenyl)-4-(dimethylamino)-1-(2-phenylethyl)cyclohexanol

Several related analogs such as the p-methyl and ring-unsubstituted compounds have also been investigated. BDPC is the lead compound in this series that attracted so much interest in it initially. narcotic analgesic A large number of analogs have been prepared, and the SAR is very well established. Lednicer constructed Dreiding models to show that the model of BDPC will give an exact overlay on a model of fentanyl.

Lednicer’s two parent compounds for BDPC. They are equipotent, arylcyclohexylamine chemical structure which is an unusual case for a simple cyclohexanone to display interchangeable equal potency with either a methyl or bromine in the same substitution, both having the same potency as pethidine. The p-Methyl was never tested as an analogue of BDPC because ‘We forgot’. acetylfentanyl Although Lednicer stated that he felt that the p-Me would be equipotent.

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