Λεπτομέρειες για το προϊόν
Τόπος καταγωγής: Κίνα
Μάρκα: Sunshine
Πιστοποίηση: ISO,COA
Αριθμό μοντέλου: 477600-75-2
Όροι πληρωμής και αποστολής
Ποσότητα παραγγελίας min: Διαπραγμάτευση
Τιμή: negotiable
Συσκευασία λεπτομέρειες: Αλουμινένιο χαρτί, βαρέλι
Χρόνος παράδοσης: 7-15 ημέρες
Όροι πληρωμής: Λ/Κ, D/A, D/P, T/T, Western Union, MoneyGram
Δυνατότητα προσφοράς: Γ,ΚΓ,ΤΟΝ
Εμφάνιση:: |
Αχνή πούδρα |
Αριθμός CAS:: |
477600-75-2 |
Μοριακός τύπος:: |
C16H20N6O |
Μοριακό βάρος:: |
312.37000 |
Αριθμός EINECS:: |
689-145-4 |
Αριθμός MDL:: |
MFCD11035919 |
Εμφάνιση:: |
Αχνή πούδρα |
Αριθμός CAS:: |
477600-75-2 |
Μοριακός τύπος:: |
C16H20N6O |
Μοριακό βάρος:: |
312.37000 |
Αριθμός EINECS:: |
689-145-4 |
Αριθμός MDL:: |
MFCD11035919 |
Product Description:
Product Name: Tofacitinib citrate CAS NO: 477600-75-2
Synonyms:
(3R,4R)-4-methyl-3-(methyl-1H-pyrrolo[2,3-d]pyrimidin-4-ylamino)-β-oxo-1-p-iperidinepropanenitrile;
Tofacitinib;
Tasocitinib;
Chemical & Physical Properties:
Appearance: Pale powder
Assay :≥99.0%
Density: 1.296g/cm3
Boiling Point: 585.845℃ at 760 mmHg
Flash Point: 308.108℃
Refractive Index: 1.646
Vapor Pressure: 0.0±1.6 mmHg at 25℃
Safety Information:
HS Code: 29335990
Signal Word: Warning
Hazard Statements: H315; H319; H335
Precautionary Statements:
P261; P264; P271; P280; P302+P352; P304+P340; P305+P351+P338; P312; P321; P332+P313; P337+P313; P362; P403+P233; P405; P501
CP-690550 is a pyrrolo[2,3-d]pyrimidine derivative, as Janus kinase inhibitor for treatment of rheumatoid arthritis.
The chemical system name of Tofacitinib citrate is 3-{(3R, 4R) -4-methyl-3 -[methyl -(7H-pyrronozo [2,3-d] pyrimidine-4-yl) -p-iperidine-1-yl] -3-oxo-propionitrile citrate, Chemicalbook is a Janus kinase inhibitor developed by Pfizer (USA). On November 6, 2012, the U.S. Food and Drug Administration (FDA) approved the drug for the treatment of adults with moderately to severely active rheumatoid arthritis (RA) who have an inadequate response or intolerance to methotrexate therapy. Tofatib is indicated for adult patients with moderately to severely active rheumatoid arthritis (RA) who have inadequate or intolerant MTX response and may be used in combination with MTX or other abiotic ameliorating antirheumatic agents (DMARDs).
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