1-(1-Adamantylcarbonyl) proline (ACA) mea hana pauka CAS No.: 35084-48-1 98% maemae min. no nā mea hoʻohui
Video Huahana
Nā Kūlana Huahana
inoa huahana | 1-(1-Adamantylcarbonyl) proline |
inoa ʻē aʻe | 1-(1-ADAMANTYLCARBONYL)PYRROLIDINE-2-CARBOXYLIC ACID; 1-(ADAMANTANE-1-CARBONYL)-PYRROLIDINE-2-CARBOXYLIC ACID; 1-(1-Adamantylcarbonyl)proline;L-Proline, 1-(tricyclo[3.3.1.13,7]dec-1-ylcarbonyl)- |
CAS No. | 35084-48-1 |
ʻAno molekala | C16H23NO3 |
Kaumaha molekula | 277.36 |
Maemae | 98.0% |
Ka nana aku | Pauda keʻokeʻo |
Hoʻopili | 1kg / ʻeke 10kg / pahu 25kg / pahu |
Palapala noi | Nootropic |
Hoʻolauna huahana
1-(1-Adamantylcarbonyl) proline he phenylalanine derivative, ʻike ʻia ʻo adamantylproline a i ʻole Ad-Pro. Hoʻohana nui ʻia e like me catalyst a i ʻole chiral resolution reagent i ka synthesis organik. Ua hōʻike mai nā haʻawina e hiki i ka 1-(1-Adamantylcarbonyl) proline ke hoʻopili 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 ka sulfuryl folate, ka hopena o nā aldehydes a me ka nitro Methane reactions, etc. ʻO ka hana hoʻohui ikaika loa kēia mea hoʻohui i nā alkylene azides. Hiki i ka 1-(1-Adamantylcarbonyl) proline ke hoʻoikaika i nā hopena amination asymmetric. Hiki ke hoʻohana ʻia ka proline 1-(1-Adamantylcarbonyl) ma ke ʻano he chiral catalyst e hoʻokaʻawale i ka asymmetric alcoholization. No ka laʻana, hiki iā ia ke hana i nā ʻawaʻawa me nā aldehydes a i ʻole nā ketones e hāʻawi i nā huahana aldol a i ʻole hydroxyketone pili. 1-(1-Adamantylcarbonyl) proline, ma ke ʻano he chiral organic compound, he hana catalytic maikaʻi loa.
Hiʻona
(1) 1-(1-Adamantylcarbonyl) proline he pauka keʻokeʻo a keʻokeʻo paha me ka solubility maikaʻi. He haʻahaʻa kona hoʻoheheʻe ʻana i ka wai akā loaʻa pinepine ka solubility maikaʻi i nā mea hoʻoheheʻe organik. He hui paʻa ia e hiki ke mālama ʻia ma ka lumi wela no ka manawa lōʻihi.
(2) 1-(1-Adamantylcarbonyl) proline he mole kiral me ʻelua enantiomers. Hoʻohana nui ʻia kona ʻano chiral i ka synthesis chiral. ʻO ka maʻamau, hoʻokahi wale nō isomer chiral e hoʻohana ʻia ma muli o kona hoʻokomo ʻana chiral maikaʻi.
(3) Maʻemaʻe kiʻekiʻe: 1-(1-Adamantylcarbonyl) proline hiki ke loaʻa nā huahana maʻemaʻe kiʻekiʻe ma o ka hoʻomaʻemaʻe ʻana i nā kaʻina hana. ʻO ka maʻemaʻe kiʻekiʻe, ʻoi aku ka maikaʻi o ka bioavailability a me ka liʻiliʻi o nā hopena ʻino.
(4) Paʻa: 1-(1-Adamantylcarbonyl) proline he kūpaʻa maikaʻi a hiki ke mālama i kāna hana a me ka hopena ma lalo o nā kaiapuni like ʻole a me nā kūlana mālama.
Nā noi
ʻO 1-(1-Adamantylcarbonyl) proline he mea hoʻohui i loko o ka nitrogen, keʻokeʻo a i ʻole ka pauka keʻokeʻo, hoʻohana ʻia ma ke ʻano he waena a me nā noi ʻē aʻe i ka lāʻau lapaʻau. Eia kekahi, ma muli o kāna mau waiwai chiral kū hoʻokahi, hoʻohana nui ʻia ia i ka chiral organic synthesis, me ka asymmetric nucleophilic hoʻohui i nā hopena, amination reactions, alcoholization reactions, etc.