Methyl 2-Oxoindoline-6-Carboxylate CAS 14192-26-8 Purity >99.0% (HPLC) Nintedanib Esylate Intermediate Factory
Ang Shanghai Ruifu Chemical Co., Ltd. ay ang nangungunang tagagawa at supplier ng Methyl 2-Oxoindoline-6-Carboxylate (CAS: 14192-26-8) na may mataas na kalidad, komersyal na produksyon.
Pangalan ng kemikal | Methyl 2-Oxoindoline-6-Carboxylate |
Mga kasingkahulugan | 2-Oxoindoline-6-Carboxylic Acid Methyl Ester;Methyl Oxindole-6-Carboxylate |
Numero ng CAS | 14192-26-8 |
Numero ng CAT | RF-PI1524 |
Katayuan ng Stock | Sa Stock, Production Scale Hanggang Tonelada |
Molecular Formula | C10H9NO3 |
Molekular na Timbang | 191.19 |
Temperatura ng pagkatunaw | 184.0~190.0 ℃ |
Tatak | Ruifu Chemical |
item | Mga pagtutukoy |
Hitsura | Banayad na Dilaw hanggang Kayumangging Pulbos |
1 H NMR Spectrum | Naaayon sa Istruktura |
Kadalisayan / Paraan ng Pagsusuri | >99.0% (HPLC) |
Pagkawala sa Pagpapatuyo | <1.00% |
Kabuuang mga Dumi | <1.00% |
Pamantayan sa Pagsubok | Enterprise Standard |
Paggamit | Intermediate ng Nintedanib Esylate (CAS: 656247-18-6) |
Methyl 2-Oxoindoline-6-Carboxylate (CAS: 14192-26-8) Synthetic na Ruta
Package: Bote, Aluminum foil bag, 25kg/Cardboard Drum, o ayon sa pangangailangan ng customer.
Kondisyon ng Imbakan:Mag-imbak sa mga selyadong lalagyan sa malamig at tuyo na lugar;Protektahan mula sa liwanag at kahalumigmigan.
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Ang Methyl 2-Oxoindoline-6-Carboxylate (CAS: 14192-26-8) ay isang intermediate na ginagamit sa paghahanda ng Nintedanib Esylate (CAS: 656247-18-6).Ang Nintedanib Esylate ay isang potent, oral triple angiokinase inhibitor na binuo ni Boehringer Ingelheim na nagta-target ng proangiogenic at pro-fibrotic pathways na pinapamagitan ng vascular endothelial growth factor receptor, fibroblast growth factor receptor at plateletderived growth factor receptor na mga pamilya, gayundin ang Src at Flt-3 kinases.Ang Nintedanib Esylate ay inaprubahan para sa paggamot ng idiopathic pulmonary fibrosis (IPF), isang kondisyon kung saan ang mga baga ay unti-unting nagiging peklat sa paglipas ng panahon, ng US FDA noong Oktubre 2014 at ng EMA noong Enero 2015. Binigyan ng FDA ang nintedanib esylate ng mabilis na track , priority review, orphan product, at breakthrough designations.Inaprubahan din ito ng EMA noong Nobyembre 2014 para sa paggamot ng non-small cell lung cancer kasama ng docetaxel pagkatapos ng first-line na chemotherapy.
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