(R)-(-)-3-Quinuclidinol CAS 25333-42-0 Ubunyulu ≥99.0% Chiral Purity ≥99.0%
Igama leMchiza | (R)-(-)-3-Quinuclidinol |
Izithethantonye | (R)-3-Quinuclinol |
Inombolo yeCAS | 25333-42-0 |
Inombolo yeCAT | RF-CC117 |
Ubume beStokhwe | Kwi-Stock, iMveliso yoMveliso ukuya kwiiToni |
Ifomula yeemolekyuli | C7H13NO |
Ubunzima beMolekyuli | 127.18 |
Uphawu | Ruifu Chemical |
Into | Iinkcukacha |
Imbonakalo | Umgubo oMhlophe okanye oMhlophe |
Ukuchongwa kwe-RT (ngu-GC) | Thobela uMgangatho weReference |
Indawo yokunyibilika | 212.0~224.0℃ |
Ukujikeleziswa okuthe ngqo [α]D20 | -40.0 ° ~ -48.0 ° |
Ukufuma (KF) | ≤0.50% |
Intsalela kwi-Ignition | ≤0.50% |
Ubunyulu | ≥99.0% |
Ukungcola ngokupheleleyo | ≤1.00% |
Ucoceko lweChiral | ≥99.0% |
I-Enantiomer | ≤1.00% |
Isivavanyi | 98.0%~101.0% (kwisiseko esingenamanzi) |
Umgangatho woVavanyo | Umgangatho woShishino |
Ukusetyenziswa | IiCompounds zeChiral;AbaPhakathi bamayeza |
Iphakheji: Ibhotile, ingxowa yefoyile yeAluminiyam, 25kg/Igubu lekhadibhodi, okanye ngokwemfuno yomthengi
Imeko yoGcino:Gcina kwizikhongozeli ezivaliweyo kwindawo epholileyo neyomileyo;Khusela ukukhanya kunye nokufuma
I-Shanghai Ruifu Chemical Co., Ltd. ngumenzi okhokelayo kunye nomthengisi we-(R)-(-)-3-Quinuclidinol (CAS: 25333-42-0) enomgangatho ophezulu, esetyenziswa ngokubanzi kwi-organic synthesis, i-synthesis ye-pharmaceutical intermediates kunye. I-Active Pharmaceutical Ingredient (API) synthesis.(R)-(-)-3-Quinuclidinol ingasetyenziswa njengendawo ephakathi kwi-synthesis ye-API (CAS: 242478-38-2).(I-CAS: 242478-38-2) iyeza le-antimuscarinic elisetyenziselwa ukunyanga i-bladder esebenzayo ebangela iimpawu zokuphindaphinda, ukukhawuleza, okanye ukungazinzi.(I-CAS: i-242478-38-2) i-M3 ye-muscarinic receptor antagonist eyaphuhliswa kwaye yaqaliswa kunyango lwe-bladder overactive (pollakiuria) eYurophu.Ii-receptors ze-M3 ziye zabandakanyeka kwi-neurally evoked smooth muscle contractions of the bladder, kunye ne-M2 receptors baye bakrokrelwa ukuba badlala indima ngenxa yokulawula kwabo kwi-detrusor muscle.I-synthesis ye-solifenacin ibandakanya ukulungiswa kwe-racemic 1-Phenyl-1,2,3,4-Tetrahydroisoquinoline ngokusebenzisa i-cyclization ye-N-(2-Phenylethyl)benzamide, kunye nokusabela okulandelayo kunye ne-ethyl chloroformate kunye ne-transesterification nge (R) -3-Quinuclidinol. .Ichromatography yeChiral inika ukubekwa wedwa kwe-diastereomer efunwayo.Ngaphandle koko, i-1-Phenyl-1,2,3,4-Tetrahydroisoquinoline inokuthi ifakwe kwisisombululo se-optical kunye (+) -i-Tartaric Acid ngaphambi kokuba unyango lwe-ethyl chloroformate kunye ne-transesterification elandelayo.