A compound of Formula I, wherein R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5 and R.sub.6 are independently hydrogen, halogen, an unsubstituted alkyl, alkenyl, alkynyl, cydoalkyi, cydoalkylalkyi, aryl, phenyl, or naphthyl group, and a substituted alkyl, alkenyl, alkynyl, cydoalkyi, cydoalkylalkyi, aryl, phenyl, or naphthyl group having as a substituent a halogen, alkoxy, substituted phenoxy, unsubstituted phenoxy group or a heteroatom such as oxygen, sulfur, nitrogen, phosphorus and boron.

##STR00001##

A compound of Formula I, wherein R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5 and R.sub.6 are independently hydrogen, halogen, an unsubstituted alkyl, alkenyl, alkynyl, cydoalkyi, cydoalkylalkyi, aryl, phenyl, or naphthyl group, and a substituted alkyl, alkenyl, alkynyl, cydoalkyi, cydoalkylalkyi, aryl, phenyl, or naphthyl group having as a substituent a halogen, alkoxy, substituted phenoxy, unsubstituted phenoxy group or a heteroatom such as oxygen, sulfur, nitrogen, phosphorus and boron.

##STR00001##

A method performing a Friedel-Crafts alkylation reaction between a dichloroalkane and an alkylbenzene produces a compound for hair regrowth. The inventive subject matter further includes incorporation of such compounds in topical formulations with suitable carriers. The resulting topical formulations may be employed in methods of stimulating hair regrowth.

A method performing a Friedel-Crafts alkylation reaction between a dichloroalkane and an alkylbenzene produces a compound for hair regrowth. The inventive subject matter further includes incorporation of such compounds in topical formulations with suitable carriers. The resulting topical formulations may be employed in methods of stimulating hair regrowth.

The present invention relates to a bicyclic compound of Formula (I) and to a composition for a cosmetic and therapeutic use and to a composition comprising an acceptable vehicle and an effective amount of the compound of Formula (I): ##STR00001##

The present invention relates to a bicyclic compound of Formula (I) and to a composition for a cosmetic and therapeutic use and to a composition comprising an acceptable vehicle and an effective amount of the compound of Formula (I): ##STR00001##

A method for extraction of desirable comounds from cannabis provides for high-cannabinoid full spectrum (HCFSE) extractions, using CO.sub.2 at low temperature to extract the compounds in an extraction vessel. The CO.sub.2 with extracted compounds is transferred to a heated vessel which converts the CO.sub.2 to a gas, allowing the desired compounds to drop out and be removed.

A method for extraction of desirable comounds from cannabis provides for high-cannabinoid full spectrum (HCFSE) extractions, using CO.sub.2 at low temperature to extract the compounds in an extraction vessel. The CO.sub.2 with extracted compounds is transferred to a heated vessel which converts the CO.sub.2 to a gas, allowing the desired compounds to drop out and be removed.

A method for extraction of desirable compounds from cannabis provides for high-cannabinoid full spectrum (HCFSE) extractions, using CO.sub.2 at low temperature to extract the compounds in an extraction vessel. The CO.sub.2 with extracted compounds is transferred to a heated vessel which converts the CO.sub.2 to a gas, allowing the desired compounds to drop out and be removed.

A method for extraction of desirable compounds from cannabis provides for high-cannabinoid full spectrum (HCFSE) extractions, using CO.sub.2 at low temperature to extract the compounds in an extraction vessel. The CO.sub.2 with extracted compounds is transferred to a heated vessel which converts the CO.sub.2 to a gas, allowing the desired compounds to drop out and be removed.