2-Chloro-5-Iodobenzoic Acid CAS 19094-56-5 Empagliflozin Intermediate Assay ≥99.0% (HPLC)
Ukunikezwa Komkhiqizi, Ukuhlanzeka Okuphezulu, Ukukhiqizwa Kwezohwebo
Igama Lekhemikhali: 2-Chloro-5-Iodobenzoic Acid
CAS: 19094-56-5
Igama Lekhemikhali | I-2-Chloro-5-Iodobenzoic Acid |
Inombolo ye-CAS | 19094-56-5 |
Inombolo yeCAT | I-RF-PI438 |
Isimo Sesitoko | Esitokweni, Isikali Sokukhiqiza Sifinyelela Kumathani |
I-Molecular Formula | I-C7H4ClIO2 |
Isisindo samangqamuzana | 282.46 |
Ukuncibilika | I-Soluble ku-Methanol |
Ibhrendi | I-Ruifu Chemical |
Into | Imininingwane |
Ukubukeka | Amakristalu Aphuzi Amhlophe noma Aphaphathekile |
Indlela Yokuhlola / Yokuhlaziya | ≥99.0% (HPLC) |
I-Melting Point | 161.0~163.0℃ |
Ukulahlekelwa Ekumisweni | ≤0.50% |
Izinsalela ekushiseni | ≤0.20% |
Ukungcola Okuphelele | ≤1.0% |
Izinsimbi Ezisindayo | ≤20ppm |
I-Residual Solvent | I-Ethanol |
Izinga Lokuhlola | I-Enterprise Standard |
Ukusetshenziswa | I-Epagliflozin emaphakathi (CAS: 864070-44-0) |
I-2-Chloro-5-Iodobenzoic Acid (CAS 19094-56-5) Umzila Wokwenziwa
Iphakheji: Ibhodlela, isikhwama se-Aluminium foil, 25kg/Cardboard Drum, noma ngokwezidingo zekhasimende.
Isimo Sesitoreji:Gcina ezitsheni ezivaliwe endaweni epholile neyomile;Vikela ekukhanyeni nakumswakama.
I-2-Chloro-5-Iodobenzoic Acid (CAS: 19094-56-5) ingasetshenziswa njengendawo yezemithi ekuhlanganiseni kwe-Empagliflozin (CAS: 864070-44-0).I-Empagliflozin (igama lokuhweba elithi Jardiance) iyi-inhibitor ye-sodium glucose co-transporter-2 (SGLT-2), futhi ibangela ukuthi ushukela osegazini ukhishwe yizinso futhi uphume emchamweni.Ngo-Agasti 1, 2014, i-Food and Drug Administration (FDA) yagunyaza ngokusemthethweni umuthi wokwelapha uhlobo lwesifo sikashukela sohlobo 2, ukuthuthukisa nokulawula ushukela wegazi kubantu abadala.I-Empagliflozin imithi yesithathu evimbela i-SGLT-2 egunyazwe yi-FDA.Eminye imithi emibili ye-SGLT-2 inhibitor, i-Canagliflozin ne-Dapagliflozin, okungekaJohnson Pharmaceuticals, i-AstraZeneca kanye ne-Bristol-Myers Squibb ngokulandelana, igunyazwe yi-FDA ngoNovemba 2013 nangoJanuwari 2014 ngokulandelana.