Mea hana pauka 1-(1-Adamantylcarbonyl)proline (ACA) CAS No.: 35084-48-1 98% maʻemaʻe min. no nā mea hoʻohui
Wikiō Huahana
Nā Palena Huahana
| Inoa huahana | 1-(1-Adamantylcarbonyl) proline |
| Inoa ʻē aʻe | 1-(1-ADAMANTYLCARBONYL)PIRROLIDINE-2-CARBOXYLIC ACID; 1-(ADAMANTANE-1-CARBONYL)-PIRROLIDINE-2-CARBOXYLIC ACID; 1-(1-Adamantylcarbonyl)proline;L-Proline, 1-(tricyclo[3.3.1.13,7]dec-1-ylcarbonyl)- |
| Helu CAS. | 35084-48-1 |
| ʻO ke ʻano molekole | C16H23NO3 |
| Kaumaha molekole | 277.36 |
| Maʻemaʻe | 98.0% |
| helehelena | Pauka keʻokeʻo |
| Hoʻopili ʻana | 1kg/ʻeke 10kg/pahu 25kg/pahu |
| Noi | Nootropic |
Hoʻolauna huahana
ʻO 1-(1-Adamantylcarbonyl) proline kahi phenylalanine derivative, i ʻike ʻia hoʻi ʻo adamantylproline a i ʻole Ad-Pro. Hoʻohana nui ʻia ma ke ʻano he catalyst a i ʻole chiral resolution reagent i ka synthesis organik. Ua hōʻike ʻia nā haʻawina e hiki i ka 1-(1-Adamantylcarbonyl) proline ke hoʻoulu i nā hopena hoʻohui nucleophilic asymmetric, e like me ka hopena o nā aldehydes a me nā alkylene azides, ka hopena o nā aldehydes a me sulfuryl folate, ka hopena o nā aldehydes a me nā nitro Methane reactions, a pēlā aku. Ma waena o kēia mau hopena, ʻo kēia catalyst ka hana hoʻohui ikaika loa i nā alkylene azides. Hiki i ka 1-(1-Adamantylcarbonyl) proline ke hoʻoulu i nā hopena amination asymmetric. Hiki ke hoʻohana ʻia ka 1-(1-Adamantylcarbonyl) proline ma ke ʻano he catalyst chiral e hoʻoulu i ka asymmetric alcoholization. No ka laʻana, hiki iā ia ke hoʻoulu i nā alcohols me nā aldehydes a i ʻole ketones e hua mai i nā huahana aldol a i ʻole hydroxyketone e pili ana. ʻO 1-(1-Adamantylcarbonyl) proline, ma ke ʻano he hui organik chiral, he hana catalytic maikaʻi loa.
Hiʻona
He pauka keʻokeʻo a keʻokeʻo paha ka (1)1-(1-Adamantylcarbonyl) proline me ka solubility maikaʻi. He haʻahaʻa kona solubility i ka wai akā pinepine he solubility maikaʻi i nā mea hoʻoheheʻe organik. He hui paʻa ia e hiki ke mālama ʻia ma ka mahana o ka lumi no ka manawa lōʻihi.
(2) ʻO 1-(1-Adamantylcarbonyl) proline kahi molekole chiral me ʻelua enantiomers. ʻO kona ʻano chiral e hoʻohana nui ʻia ai i ka hana chiral. Ma ke ʻano laulā, hoʻokahi wale nō isomer chiral e hoʻohana ʻia ma muli o kona hoʻokomo chiral maikaʻi.
(3) Maʻemaʻe kiʻekiʻe: Hiki i ka 1-(1-Adamantylcarbonyl) proline ke loaʻa nā huahana maʻemaʻe kiʻekiʻe ma o nā kaʻina hana hoʻomaʻemaʻe. ʻO ke ʻano o ka maʻemaʻe kiʻekiʻe ʻo ia hoʻi ka bioavailability maikaʻi a me nā hopena ʻino liʻiliʻi.
(4) Paʻa: Loaʻa i ka 1-(1-Adamantylcarbonyl) proline ke kūpaʻa maikaʻi a hiki ke mālama i kāna hana a me kona hopena ma lalo o nā ʻano like ʻole a me nā kūlana mālama.
Nā noi
ʻO 1-(1-Adamantylcarbonyl) proline kahi hui organik i loaʻa ka naikokene, pauka keʻokeʻo a keʻokeʻo paha, i hoʻohana ʻia ma ke ʻano he waena a me nā noi ʻē aʻe i ka lāʻau lapaʻau. Eia kekahi, ma muli o kona mau waiwai chiral kū hoʻokahi, hoʻohana nui ʻia ia i ka synthesis organik chiral, me nā hopena hoʻohui nucleophilic asymmetric, nā hopena amination, nā hopena alcoholization, a pēlā aku.
